Acessibilidade / Reportar erro

Skin manifestations associated with COVID-19* * Study conducted at the Department of Dermatology, Universidade Federal de São Paulo, São Paulo, SP, Brazil.

Abstract

This article will address the main aspects of skin manifestations associated with COVID-19, based on a review of the literature published to date. Since the beginning of the pandemic, more than 1,500 articles have been published on the subject. Regarding the pathophysiology, it is believed that the same mechanisms responsible for the disease in the main target organs also act in the skin, although they are not yet fully elucidated. The actual frequency of dermatological manifestations remains uncertain - it can range from 0.2% to 45%, being close to 6% in systematic reviews. Pioneering studies of large case series conducted in European countries and the USA provide the first information on the main skin manifestations associated with COVID-19 and propose classifications regarding their clinical presentation, pathophysiology, as well as their frequencies. Although there is yet no consensus, maculopapular eruptions are considered the most frequent presentations, followed by erythema pernio-like (EPL) lesions. Manifestations such as urticaria, vesicular conditions and livedo/purpura/necrosis are rare. The time of onset, severity, need for specific treatment and prognosis vary according to the clinical presentation pattern. The increasing histopathological description of skin conditions can contribute to the diagnosis, as well as to the understanding of the pathophysiology. Also, in the dermatological field, the relationship between COVID-19 and androgens has been increasingly studied. Despite all the generated knowledge, the actual biological meaning of skin manifestations remains uncertain. Therefore, the exclusion of the main differential diagnoses is essential for the correlation between skin manifestation and COVID-19.

KEYWORDS
COVID-19; Dermatology; Skin

Introduction

At the beginning of the COVID-19 pandemic, skin lesions weree already considered to be important among the clinical manifestations of this new disease. Since March 2020, more than 1,500 articles correlating ‘‘dermatology’’ and ‘‘COVID-19’’ have been published. Never has such a large amount of information been generated in such a short time in the scientific community, including dermatology-related data. Although the first reports were poorly informative, possibly due to the inability to perform a complete dermatological examination, photographic record, histopathological and/or immunohistochemical analysis, and the scarcity of specialists in direct assistance to these patients, subsequent research has produced important contributions on the cutaneous involvement in COVID-19.11 Shinkai K, Bruckner AL. Dermatology and COVID-19. JAMA.2020;324:1133-4. In this document, the main publications to date (04/30/21) on different aspects of the dermatological manifestations of COVID-19 will be reviewed, according to the methodologies adopted in these studies. Pubmed was used as a database, using the following keywords: COVID-19, SARS-CoV-2, ‘‘dermatology’’, ‘‘skin’’. The initial information is shown in Table 1 (Capsule with the main key points).

Table 1
Capsule with the main key points.

Frequency of cutaneous manifestations associated with COVID-19

Although the first report in the literature of a dermatological condition possibly associated with COVID-19 was published on 03/22/20 by Joob and Wiwanitkit22 Joob B, Wiwanitkit V. COVID-19 can present with a rash and bemistaken for dengue. J Am Acad Dermatol. 2020;82:177. in the Journal of the American Academy of Dermatology (JAAD), in late 2019, Guan et al.33 Guan WJ, Ni ZY, Hu Y, Liang WH, Ou CQ, He JX, et al. ClinicalCharacteristics of Coronavirus Disease 2019 in China. N Engl JMed. 2020;382:1708-20. made the first citation about the frequency of cutaneous manifestations. Of the 1,099 described patients with SARS-CoV-2 infection, 0.2% had a rash.

The first article focusing mainly on the frequency of cutaneous manifestations, published by Recalcati44 Recalcati S. Cutaneous manifestations in COVID-19: a first per-spective. J Eur Acad Dermatol Venereol. 2020;34:212-3. on 03/26/20, reported that of 88 cases evaluated by dermatologists, 20.4% had skin lesions. Since then, the estimation of such frequency has been widely variable, in different countries, according to data obtained through different methodologies. Matar et al.55 Matar S, Oulès B, Sohier P, Chosidow O, Beylot-Barroy M, Dupin N, et al. Cutaneous manifestations in SARS-CoV-2 infection(COVID-19): a French experience and a systematic review ofthe literature. J Eur Acad Dermatol Venereol. 2020;34:686-9. in France, Reknimitr et al.66 Rerknimitr P, Theerawattanawit C, Lertpichitkul P, Jan-tarabenjakul W, Putcharoen O, Puthanakit T, et al. Skinmanifestations in COVID-19: The tropics experience. J Derma-tol. 2020;47:444-6. in Thailand, and Solak et al.77 Solak EO, Ketencioglu BB, Aslaner H, Çinar SL, Kartal D, Benli AR, et al. Cutaneous symptoms of patients diagnosed withCOVID-19 in one province: a cross-sectional survey. J Eur AcadDermatol Venereol. 2021;35:105-6. in Turkey have shown frequencies of 1% (n = 756), 15% (n = 183), and 18.3% (n = 382), respectively, through remote collection of data through telephone interviews after evaluation performed by the patient (selfexamination). Lower frequencies were recorded by Gaspari et al.88 Gaspari V, Orioni G, Misciali C, Viviani F, Zengarini C. COVID-19skin eruptions: incidence in hospitalized patients in Bologna. IntJ Dermatol. 2021;60:512-3. in Italy (1.4%), Tammaro et al.99 Tammaro A, Adebanjo GAR, Parisella FR, Pezzuto A, RelloJ. Cutaneous manifestations in COVID-19: the experiencesof Barcelona and Rome. J Eur Acad Dermatol Venereol.2020;34:306-7. also in Italy (1.5%, n=130), and Tamai et al.1010 Tamai M, Maekawa A, Goto N, Ge L, Nishida T, Iwahashi H, et al.Three cases of COVID-19 patients presenting with erythema. JDermatol. 2020;47:1175-8. in Japan (4.3%, n=69) through in-person evaluation of patients performed by a dermatologist, a crucial factor for greater sensitivity in detecting skin lesions and accuracy in attributing them to COVID-19. Using the most appropriate methodology, it is believed that the actual frequency is close to those reported by these latest studies. The main criticisms of the initial studies are remote evaluation, assessment by the patients themselves or by health professionals who were not dermatologists, the inclusion of suspected cases of COVID-19 (unconfirmed), and not excluding common skin conditions, such as other viral infections and adverse drug reactions. The actual biological meaning of these manifestations still seems uncertain. More data on frequency will be cited below in the topics ‘‘Prospective studies’’ and ‘‘Systematic reviews’’ and summarized in Table 2 (frequency of dermatological manifestations in COVID-19).

Table 2
Frequency of dermatological manifestations in COVID-19.

Interestingly, a Spanish study showed that the frequency of dermatological manifestations was even lower in the second wave of the epidemic in that country.1111 Fernandez-Guarino M, Ortega-Quijano D, Suarez-Valle A,Jimenez-Cauhe J, Jaen-Olasolo P, Fernandez-Guarino M, et al.Lack of skin manifestations in COVID-19 hospitalized patientsduring the second epidemic wave in Spain: a possible associa-tion with a novel SARS-CoV-2 variant a cross sectional study. JEur Acad Dermatol Venereol. 2021;35:183-5. Possible explanations are: better knowledge about the disease allowed early treatment and more assertive treatment, which reduced the proportion of severe cases and adverse drug reactions (one of the main differential diagnoses); greater application of preventive measures and diagnostic tests to exclude other viral infections; new mutations with a greater diversity of virulence and antigenicity. Furthermore, the apparent low frequency of dermatological lesions compared to ‘‘classic’’ clinical manifestations can be explained by the lower expression of viral receptors in the skin compared to other target organs and by the presence of membrane proteases with a protective action on the skin.1212 Criado PR, Pincelli TPH, Criado RFJ, Abdalla BMZ, Belda JuniorW. Potential interactions of SARS-CoV-2 with human cell recep-tors in the skin: Understanding the enigma for a lower frequencyof skin lesions compared to other tissues. Exp Dermatol.2020;29:936-44.

Finally, a recent Austrian study with case-control methodology did not show any statistical significance comparing the presence of skin lesions in the group of patients with confirmed COVID-19 (cases) and in the non-COVID group (controls).1313 Unterluggauer L, Pospischil I, Krall C, Saluzzo S, Kimeswenger S,Karolyi M, et al. Cutaneous manifestations of SARS-CoV-2 a two-center, prospective, case-controlled study. J Am Acad Dermatol.2021;85:202-4. It is suggested that skin lesions are less specific than other clinical signs, are not good diagnostic clues, should be evaluated carefully, and be attributed to COVID19 only after ruling out other differential diagnoses, such as adverse drug reactions and other viral infections.

Pathophysiology

The mechanisms by which SARS-CoV-2 causes disease in different organs, including the skin, are quite complex and not yet fully understood.

The risk for an organ to develop SARS-CoV-2 infection is determined by the presence of functional ACE2 (angiotensin-converting enzyme 2) and TMPRSS2 (transmembrane protease serine 2) viral receptors expressed on local cells. ACE2 is found mainly in alveolar epithelial cells, explaining the high vulnerability of the lungs to COVID-19. Some studies have shown that ACE2 is detectable in the basal layer of the epidermis, as well as in hair follicles. However, the presence of SARS-CoV-2 in skin samples has been related to the expression of ACE2 in cutaneous capillary endothelial cells, not in keratinocytes and melanocytes,1414 Bourgonje AR, Abdulle AE, Timens W, Hillebrands JL, Navis GJ, Gordijn SJ, et al. Angiotensin-converting enzyme 2 (ACE2),SARS-CoV-2 and the pathophysiology of coronavirus disease 2019(COVID-19). J Pathol. 2020;251:228-48. which makes the virus unable to penetrate and infect directly and primarily the skin. Skin involvement is indirect, and it occurs due to infection of the endothelial cells of the dermal vessels. The presence of SARS-CoV-2 in skin lesions has been previously confirmed by the PCR (polymerase chain reaction) technique in tissue with low replication, even in patients with negative PCR in the nasal swab and serology, showing that the skin can be an infected organ, and eventually even a diagnostic one.1515 Jamiolkowski D, Mühleisen B, Müller S, Navarini AA, Tzankov A,Roider E. SARS-CoV-2 PCR testing of skin for COVID-19 diagnos-tics: a case report. Lancet. 2020;396:598-9.

The first and strongest evidence about the pathophysiology of skin lesions in COVID-19 was published by Magro et al.1616 Magro C, Mulvey JJ, Berlin D, Nuovo G, Salvatore S, Harp J, et al.Complement associated microvascular injury and thrombosis inthe pathogenesis of severe COVID-19 infection: A report of fivecases. Transl Res. 2020;220:1-13. at the beginning of the pandemic (04/15/20). Through histopathology techniques and immunohistochemical analysis of complement components and the viral spike protein, the study showed that the pathophysiological process responsible for the pulmonary involvement can also occur in the skin, both healthy and damaged, in addition to demonstrating the viral presence in these organs. Similarly, Colmenero et al.1717 Colmenero I, Santonja C, Alonso-Ria˜no M, Noguera-Morel L,Hernández-Martín A, Andina D, et al. SARS-CoV-2 endothe-lial infection causes COVID-19 chilblains: histopathological,immunohistochemical and ultrastructural study of seven pae-diatric cases. Br J Dermatol. 2020;183:729-37. also identified viral particles in the endothelium of erythema pernio-like lesions in children, which supports the causal relationship between cutaneous involvement and viral presence. SARS-CoV-2induced endothelial damage in the skin may be one of the key mechanisms in the pathogenesis.

The pathophysiology of COVID-19 is known to be multifactorial and involves the innate immune, humoral response, hypercoagulability, monocytic/macrophagic activation, significant cytokine increase (‘‘cytokine storm’’), among others.1818 Criado PR, Abdalla BMZ, Assis IC, Mello CBG, Caputo GC, VieiraIC. Are the cutaneous manifestations during or due to SARS-CoV-2 infection/COVID-19 frequent or not? Revision of possiblepathophysiologic mechanisms. Inflamm Res. 2020;69:745-56. In a rather simplified way, skin manifestations have been divided into two forms regarding the pathophysiology: (1) inflammatory, as an immune response to viral nucleotides, and (2) vascular, secondary to vasculitis, vasculopathy, and thrombosis phenomena.1919 Suchonwanit P, Leerunyakul K, Kositkuljorn C. Cutaneous mani-festations in COVID-19: Lessons learned from current evidence.J Am Acad Dermatol. 2020;83:57-60. Regarding the inflammatory response, viral infections are related to the triggering of the innate and adaptive immune responses. The monocytic-macrophage system produces an exacerbated immune response, generating an intense systemic inflammatory process. The viral activation of mast cells and basophils could justify lesions such as urticaria and exanthems.2020 Criado PR, Pagliari C, Carneiro FRO, Quaresma JAS. Lessonsfrom dermatology about inflammatory responses in Covid-19.Rev Med Virol. 2020;30:2130. Regarding the vascular mechanisms, the most often studied lesions are the erythema pernio type, in analogy to the pathophysiology of previously known diseases, such as the ‘‘classic’’ erythema pernio (triggered by cold), ‘‘lupus’’, and other vascular entities, such as livedoid vasculopathy.2121 Cavanagh G, Criado PR, Pagliari C, Carneiro FRO, Quaresma JAS,Cappel MA, et al. Pernio during the COVID-19 pandemic andreview of inflammation patterns and mechanisms of hypercoag-ulability. JAAD Case Rep. 2020;6:898-9. It is believed that erythema pernio associated with COVID19 also results from an exaggerated immune reaction with signaling via type I interferon, which is important for viral eradication, but with a generalized, highly inflammatory response. In critically ill patients with purpura, vascular thrombosis in the skin and other organs would be associated with a minimal interferon response, allowing excessive viral replication, with the release of viral proteins that are located in the extrapulmonary endothelium and trigger extensive complement activation.2222 Magro CM, Mulvey JJ, Laurence J, Sanders S, Crowson NA, Gross-man M, et al. The differing pathophysiologies that underlieCOVID-19-associated perniosis and thrombotic retiform pur-pura: a case series. Br J Dermatol. 2021;184:141-50.,2323 Santonja C, Heras F, Nú˜nez L, Requena L. COVID-19 chilblain-like lesion: immunohistochemical demonstration of SARS-CoV-2 spike protein in blood vessel endothelium and sweat glandepithelium in a polymerase chain reaction-negative patient. BrJ Dermatol. 2020;183:778-80.

Controversies regarding the pathophysiology and the presence of viral particles triggering skin lesions are based on studies that verify the absence of these particles in research, using the PCR technique in biopsies of skin lesions.2424 García-Gil MF, Monte-Serrano J, García MG, Prieto-Torres L,Pascual-Del-Riquelme AJ, Flecha IC, et al. Absence of SARS-CoV-2 RNA detection in tissue samples of COVID-19-relatedcutaneous lesions analyzed by real-time RT-PCR. J Eur AcadDermatol Venereol. 2021;35:318-21. Additionally, it has recently been suggested that SARS-CoV-2 could cause the reactivation of other latent viruses, such as HHV-6, which is the actual responsible for some skin manifestations initially attributed to COVID-19,2525 Abadías-Granado I, Navarro-Bielsa A, Morales-Callaghan AM,Roc L, Suso-Estívalez CC, Povar-Echeverría M, et al. COVID-19-associated cutaneous manifestations: does human herpesvirus6 play an aetiological role? Br J Dermatol. 2021;184:1187-90. such as exanthems and pityriasis rosea-like conditions.

Large national and international series

Soon after the first reports of isolated cases of cutaneous manifestations in patients with COVID-19, especially with the arrival of the pandemic in Europe, some countries carried out studies with national and international collaboration under the leadership of their respective academic societies. Thus, the first studies of large series of cases on the most prevalent skin manifestations were reported, including suggestions for classification into groups according to the clinical pattern and pathophysiological mechanisms. These studies were crucial for the initial understanding of the relationship between dermatology and COVID-19 and are still important references to date. The main data from these studies are shown in Table 3 (Large national and international series on skin manifestations).

Table 3
Large national and international series on skin manifestations.

Spain

The first large retrospective series was published on 04/29/20 by Galván-Casas et al,2626 Casas CG, Català A, Hernández GC, Rodríguez-Jiménez P,Fernández-Nieto D, Lario ARV, et al. Classification of thecutaneous manifestations of COVID-19: a rapid prospectivenationwide consensus study in Spain with 375 cases. Br J Der-matol. 2020;183:71-7. widely publicized, containing a dermatological atlas. With support from the Spanish Academy of Dermatology, dermatologists across the country included images of skin lesions from 375 patients with COVID-19 (suspected or confirmed), which were grouped into five main patterns: maculopapular eruptions (47%), urticarial rash (19%), EPL (19%), vesico-bullous (9%), and livedo/necrosis (6%).

The most commonly found pattern was maculopapular eruptions, showing a concomitant onset with general symptoms and an average duration of 8.6 days, similarly to urticarial conditions. Both were considered not useful for the diagnosis of COVID-19 because they are non-specific manifestations common to other common conditions, such as adverse drug reactions and other viral infections.

EPL lesions occurred in younger patients with mild systemic conditions, with a late-onset (mean of 12.7 days from the onset of general symptoms) and prolonged duration. Only one of the 71 cases reported prior erythema pernio (EP). They would be useful as an epidemiological and not a diagnostic marker.

Vesicular lesions appeared before the general symptoms in 15% of the cases in this series, with a mean duration of 10.4 days and relative diagnostic specificity since they are skin manifestations not reported in viral exanthems.

Livedo/necrosis includes a variable range of presentations related to COVID-19 or its complications, such as a hypercoagulable state and vascular damage. They are associated with an older age group and higher mortality.

Although there is great merit regarding the pioneering and significant number of cases, the study limitations are the inclusion of patients who were not confirmed cases of COVID-19 (suspected cases), mostly outpatients, evaluated photographic records, without histopathological analysis or exclusion of the main differential diagnoses.

France

On 05/04/20, de Masson et al.,2727 Masson A, Bouaziz JD, Sulimovic L, Cassius C, Jachiet M, Ionescu MA, et al. Chilblains is a common cutaneous finding duringthe COVID-19 pandemic: A retrospective nationwide study fromFrance. J Am Acad Dermatol. 2020;83:667-70. with support from the French Union of Dermatologists and Venereologists, published a retrospective observational study in letter form that included images of skin manifestations of 277 patients with COVID-19 (252 suspected and 25 confirmed cases) from private clinics throughout France. Surprisingly, EPL lesions corresponded to the vast majority of cases (75%) and were even reported as the single manifestation of the disease. Histopathology study carried out in three cases showed lichenoid interface dermatitis with the presence of microthrombi. Other identified cutaneous patterns were: vesicular (15%), urticarial (9%), morbilliform (9%), petechial (3%), livedo reticularis (1%), and others (15%). Some patients were accounted for in more than one category. It is worth remembering that the French were the first to describe EPL lesions related to COVID-19, which could be a bias for the high frequency shown in this study, non-reproducible in other similar studies. Additionally, the high prevalence of EPL lesions is probably reflected in the large percentage of unconfirmed cases included in the analysis since such lesions predominate in oligo- or asymptomatic COVID-19 cases, which are seldom tested for laboratory confirmation of SARS-CoV-2 infection.

USA/International (31 countries)

In collaboration with the American Academy of Dermatology and the International League of Dermatological Societies, Freeman et al.2828 Freeman EE, McMahon DE, Lipoff JB, Rosenbach M, Kovarik C,Desai SR, et al. The spectrum of COVID-19-associated dermato-logic manifestations: An international registry of 716 patientsfrom 31 countries. J Am Acad Dermatol. 2020;83:1118-29. collected data on 716 cases from 31 countries through an electronic registry and the results were published on 07/02/20. Dermatologists provided data on 54% of the cases, with 89% of all registries originating from the USA. Only 34 Hispanic/Latino and 13 AfricanAmerican patients were included, impairing the racial diversity required to understand the skin manifestations. Only 171 patients were confirmed COVID-19 cases, with the following frequency of manifestations: morbilliform (22%), EPL (18%), urticarial (16%), macular erythema (13%), vesicular (11%), papulo-desquamative (9.9%) and retiform purpura (6.4%). Most of the skin manifestations started concomitantly with the general symptoms; however, in 12%, the skin lesions were the first symptoms of the disease, showing the possible importance of skin lesions as a marker for the early diagnosis of COVID-19. Regarding the severity, EPL lesions were associated with milder systemic conditions, while 100% of cases with retiform purpura were hospitalized. Histopathology was carried out in 14 confirmed cases. The study limitations include evaluator bias, the impossibility of estimating the frequency/prevalence of skin manifestations, low rate of confirmed COVID-19 cases (25%), and little ethnic diversity, despite the apparent high representativeness of the 31 countries.

Italy

Similar to Spain and France, on 01/18/21, the Italian Society of Dermatology and Sexually Transmitted Disease also coordinated a national study that gathered data from 200 patients with skin manifestations. One of the inclusion criteria for Marzano et al.2929 Marzano AV, Genovese G, Moltrasio C, Gaspari V, Vezzoli P,Maione V, et al. The clinical spectrum of COVID-19-associatedcutaneous manifestations: An Italian multicenter study of 200adult patients. J Am Acad Dermatol. 2021;84:1356-63. was the presence of COVID-19-related skin lesions confirmed by an experienced dermatologist. A total of 62% had a confirmed diagnosis of COVID-19. The main identified patterns were: maculopapular eruption/morbilliform exanthem (25.7%), EPL (24.6%), papulovesicular eruption (15.5%), urticarial eruption (10.2%), purpura/vasculitis (6.9%), livedo reticularis/racemosa (2.1%) and others (15%), which included pityriasis rosea-like, erythema multiforme-like, erythema nodosum-like, panniculitis and angioedema. Mucosal lesions were not identified. The skin condition appeared on average 14 days after the onset of systemic symptoms and lasted for an average of 12 days. EPL lesions lasted longer than the other patterns, occurred in a younger age group, and represented a lower risk of developing a severe systemic disease, all factors with statistical significance. The mean age of the livedo reticularis/racemosa and maculopapular eruption/morbilliform exanthem groups was also older (p < 0.01). One limitation of the study is the lack of diagnostic confirmation of SARS-CoV-2 infection in 36.5% of the sample due to economic factors that limited the extensive diagnostic testing in Italy and in several other countries.

United Kingdom

Finally, the most recent population study, with very significant figures, whose results generated a lot of repercussions, was published on 01/14/21 by Visconti et al.,3030 Visconti A, Bataille V, Rossi N, Kluk J, Murphy R, Puig S, et al.Diagnostic value of cutaneous manifestation of SARS-CoV-2infection. Br J Dermatol. 2021;184:880-7. which included data from all over the United Kingdom and had a different design than those of the abovementioned publications.

The first arm of the study collected data from 336,847 users of the ‘‘COVID Symptom Study’’ application, in which they provided epidemiological, laboratory, and clinical information, including on the presence or absence of skin lesions identified by the users themselves. Only 2021 (7.4%) users had laboratory confirmation of COVID-19, and of these, 178 (8.8%) reported skin lesions. The prevalence was slightly higher among women. Additionally, the prevalence of skin lesions was significantly higher among those who tested positive for SARS-CoV-2 when compared to those who tested negative, justifying the inclusion of skin involvement in the list of symptoms in suspected COVID-19 infection due to its diagnostic, predictive factor, regardless of how often it occurs.

The second arm of the study sought to investigate in detail the skin manifestations through a questionnaire addressed to users who reported them and the sharing of photos. Of the 11,544 answered questionnaires, only 694 (6%) had a confirmed diagnosis of COVID-19. In this group, although the majority reported the onset of skin lesions together or soon after the general symptoms, 17% reported that the skin lesions appeared before the systemic symptoms, and in 21%, the skin condition was the only symptom. However, the study did not provide additional detailed information about these findings. There was no description of which skin manifestations occurred prior to the general symptoms and how long before they appeared. Neither did it specify which skin lesions were considered by the individual themselves as the only manifestation of COVID-19, nor did it clarify the reason why laboratory confirmation of the disease was performed in the absence of any suspected symptoms.

In this same arm of the study, 2,328 users shared photos of skin lesions; 260 images were randomly selected for analysis by dermatologists, and of these, 30 were discarded as not attributable to SARS-CoV-2 infection - examples: acne, molluscum contagiosum, herpes zoster, eczema, perioral dermatitis, impetigo, dermatophytosis, which shows the user’s own limitations as an evaluator of their skin lesions. The final images were evaluated by four experienced dermatologists. The most frequent dermatological presentations were papular eruptions (41.2% including erythematouspapular and erythematous-vesicular), urticarial (30%), and acral (23.1%) eruptions.

To date, this is the first and only impactful publication stating the frequency and relevance of skin lesions as the only manifestation of SARS-CoV-2 infection. Therefore, caution and further studies on the subject are necessary to understand its actual importance and impact on the diagnosis of COVID-19.

The nature of the study has four main limitations: data based on self-assessment, not representative of the general population, disregarding of rare dermatological manifestations, and the impossibility of ruling out important differential diagnoses, such as adverse drug reactions.

Prospective studies

There are few prospective studies on skin manifestations associated with COVID-19 that have been published to date. Such methodology would provide more reliable information about the actual prevalence of skin lesions and the identified patterns, especially through the active search for skin lesions by the specialist.

Nevertheless, different prevalence rates, proportions, and classifications of skin manifestations diagnosed by dermatologists in patients with prospectively confirmed SARS-CoV-2 infection have been reported. De Giorgi et al.3131 De Giorgi V, Recalcati S, Jia Z, Chong W, Ding R, Deng Y, et al.Cutaneous manifestations related to coronavirus disease 2019(COVID-19): A prospective study from China and Italy. J Am AcadDermatol. 2020;83:674-5. evaluated 678 patients in hospitals in Italy and China, finding a frequency of 7.8% of skin lesions, with 44% being identified at the diagnosis of COVID-19 and 56% in subsequent days, on average after 11.7 days. The most frequent finding was exanthem (70%), followed by urticarial (26%) and vesicular lesions (4%). All exanthem cases spontaneously improved within two to five days. Rehktman et al.3232 Rekhtman S, Tannenbaum R, Strunk A, Birabaharan M, Wright S, Grbic N, et al. Eruptions and related clinical course among296 hospitalized adults with confirmed COVID-19. J Am AcadDermatol. 2021;84:946-52. evaluated 296 patients in two hospitals in New York, with an 11.8% frequency of skin lesions in the following proportions: ulcers (37.1%), purpura (25.7%), necrosis (14.3%), non-specific erythema (11.4%), morbilliform eruption (11.4%), EPL (11.4%) and vesicles (2.9%). Méndez-Maestro et al.3333 Maestro IM, Merino LP, Tánago BUG, González AA, Sope˜na AO,Vicente JS, et al. Skin manifestations in patients hospitalizedwith confirmed COVID-19 disease: a cross-sectional study in atertiary hospital. Int J Dermatol. 2020;59:1353-7. evaluated 75 patients in a Spanish hospital, and 14 (18.7%) had skin lesions that were possibly associated with COVID-19, namely: EPL (42.8%), maculopapular eruption (28.6%), urticarial (14.3%), livedo reticularis-like (7.15%) and vesicular lesions (7.15%). Finally, Nuno-Gonzales et al.3434 Nuno-Gonzalez A, Martin-Carrillo P, Magaletsky K, Rios MDM,Ma˜nas CH, Almazan JA, et al. Prevalence of mucocutaneousmanifestations in 666 patients with COVID-19 in a field hos-pital in Spain: oral and palmoplantar findings. Br J Dermatol.2021;184:184-5. evaluated 666 patients, also in a hospital environment in Spain, and reported a very high frequency of 45.65% of mucocutaneous lesions. However, the study included very non-specific changes that were both mucosal (examples: papillitis, glossitis, stomatitis, depapillation, mucositis) and cutaneous (examples: erythematous-brownish palmoplantar macules).

In Brazil, there are no data so far on the prevalence of skin lesions. Avancini et al.3535 Avancini J, Miyamoto D, Arnone M, Gabbi TVB, Ferreira PS, Festa-Neto C, et al. Absence of specific cutaneous manifestations of severe acute respiratory syndrome coronavirus 2 in a reference center in Brazil. J Am Acad Dermatol. 2021;84:67. reported that of the 86 patients admitted to a referral center with a confirmed infection by SARS-CoV-2 for which an evaluation by the dermatology team was requested, it was not possible to attribute a direct correlation between skin lesions and COVID-19 in any of them, since the identified profile of dermatoses was similar to that of the pre-pandemic period. Five patients had exanthem that was indistinguishable from a drug reaction, and one had EPL lesions, but together with a personal history of systemic lupus erythematosus.

Systematic reviews

A large number of publications in a short period of time allowed the first systematic review of studies on the skin manifestations of COVID-19 to appear at the end of 2020, aiming to gather and compile the results obtained up to that time, producing data with greater scientific evidence. Still, the conclusions were divergent.

In two systematic review articles, the prevalence of skin lesions in patients with COVID-19 was quite similar: 5.69 and 5.95%.3636 Jamshidi P, Hajikhani B, Mirsaeidi M, Vahidnezhad H, Dadashi M, Nasiri MJ. Skin Manifestations in COVID-19 Patients: Are They Indicators for Disease Severity? A Systematic Review. Front Med (Lausanne). 2021;8:634208. However, even meta-analysis studies still differ as to what would be the most frequent skin manifestations. Most systematic reviews found a higher frequency of maculopapular eruptions: 37.1%, 36% and 48%, followed by vascular lesions (including EPL): 23% and 33%.3737 Gisondi P, Leo SD, Bellinato F, Cazzaniga S, Piaserico S, Naldi L. Time of Onset of Selected Skin Lesions Associated with COVID-19: A Systematic Review. Dermatol Ther (Heidelb). 2021;11:695-705. However, others claim that the most common pattern would be EPL lesions (51.5%).3838 Mirza FN, Malik AA, Omer SB, Sethi A. Dermatologic manifestations of COVID-19: a comprehensive systematic review. Int J Dermatol. 2021;60:418-50. Urticarial, vesicular, and livedo/necrosis conditions are considered rarer.3636 Jamshidi P, Hajikhani B, Mirsaeidi M, Vahidnezhad H, Dadashi M, Nasiri MJ. Skin Manifestations in COVID-19 Patients: Are They Indicators for Disease Severity? A Systematic Review. Front Med (Lausanne). 2021;8:634208.

37 Gisondi P, Leo SD, Bellinato F, Cazzaniga S, Piaserico S, Naldi L. Time of Onset of Selected Skin Lesions Associated with COVID-19: A Systematic Review. Dermatol Ther (Heidelb). 2021;11:695-705.
-3838 Mirza FN, Malik AA, Omer SB, Sethi A. Dermatologic manifestations of COVID-19: a comprehensive systematic review. Int J Dermatol. 2021;60:418-50.

In their systematic review, Jamshidi et al.3636 Jamshidi P, Hajikhani B, Mirsaeidi M, Vahidnezhad H, Dadashi M, Nasiri MJ. Skin Manifestations in COVID-19 Patients: Are They Indicators for Disease Severity? A Systematic Review. Front Med (Lausanne). 2021;8:634208. focused on prognostic factors associated with different patterns of skin manifestations. Maculopapular eruptions are associated with mild COVID-19 in 48% of cases, as well as urticarial and EPL patterns. Patients with vascular lesions of the livedo, purpura and necrosis spectrum were associated with the highest mortality (18.2%), and those with urticarial lesions, the lowest (2.2%). Regarding the time of onset of skin manifestations, the vast majority (92%) occur within four weeks of the onset of COVID-19 general symptoms, especially in the first days and up to two weeks in cases of exanthems and urticaria. On the other hand, EPL lesions occur later and appear between the second and fourth weeks, as well as purpura and necrosis. In 8 to 10%3737 Gisondi P, Leo SD, Bellinato F, Cazzaniga S, Piaserico S, Naldi L. Time of Onset of Selected Skin Lesions Associated with COVID-19: A Systematic Review. Dermatol Ther (Heidelb). 2021;11:695-705. of the cases, the skin manifestations may precede the clinical symptoms, on average, by three days, thus possibly being useful indicators for the early diagnosis of COVID-19. It is important to emphasize that almost all the studies included in the systematic reviews originate from Europe and the USA, with few reports from Asia and Latin America (due to the scarcity of published data), which could generate a bias.

Main skin manifestations associated with COVID-19

Maculopapular eruption

In most studies, it is considered the most frequent skin manifestation of COVID-19. It includes exanthem (Fig. 1), rash, diffuse papules, pityriasis rosea-like, erythema multiformelike, among others. It usually appears within the first days of the general viral infection symptoms or in up to two weeks, although there are sporadic reports of a late-onset (after one month). It correlates with mild systemic conditions and spontaneously improves within seven to ten days,2626 Casas CG, Català A, Hernández GC, Rodríguez-Jiménez P,Fernández-Nieto D, Lario ARV, et al. Classification of thecutaneous manifestations of COVID-19: a rapid prospectivenationwide consensus study in Spain with 375 cases. Br J Der-matol. 2020;183:71-7. without the need for specific treatment.

Figure 1
Exanthem in a patient with COVID-19.

Although these are frequent manifestations, they are highly non-specific, since other viral infections are common causes of exanthems, as well as adverse drug reactions. The literature discusses the need to exclude such differential diagnoses before attributing the skin condition solely to COVID-19, even in confirmed cases of the disease. Another confounding factor is the viral reactivation that occurs in cases of drug reactions, such as the activation of HHV6 in DRESS (drug reaction with eosinophilia and systemic symptoms). One hypothesis would be that the SARS-CoV-2 infection would lead to reactivation of latent viruses, such as HHV-6, and thus predispose to an adverse drug reaction.2525 Abadías-Granado I, Navarro-Bielsa A, Morales-Callaghan AM,Roc L, Suso-Estívalez CC, Povar-Echeverría M, et al. COVID-19-associated cutaneous manifestations: does human herpesvirus6 play an aetiological role? Br J Dermatol. 2021;184:1187-90.,3939 Rosell-Díaz AM, Mateos-Mayo A, Nieto-Benito LM, BalaguerFranch I, Torre-Ruiz EH, Lainez-Nuez A, et al. Exanthem and eosinophilia in COVID-19 patients: has viral infection a role in drug induced exanthems? J Eur Acad Dermatol Venereol. 2020;34:561-3.

Erythema pernio-like (EPL)

It is undeniable that this is the most often reported manifestation in large case series in the literature.4040 Fernandez-Nieto D, Jimenez-Cauhe J, Suarez-Valle A, MorenoArrones OM, Saceda-Corralo D, Arana-Raja A, et al. Characterization of acute acral skin lesions in nonhospitalized patients: A case series of 132 patients during the COVID-19 outbreak. J Am Acad Dermatol. 2020;83:61-3.,4141 Freeman EE, McMahon DE, Lipoff JB, Rosenbach M, Kovarik C, Takeshita J, et al. Pernio-like skin lesions associated with COVID-19: A case series of 318 patients from 8 countries. J Am Acad Dermatol. 2020;83:486-92. With the arrival of the COVID-19 pandemic in Europe, there was an explosion of cases similar to ‘‘classic’’ erythema pernio, but with peculiar characteristics, different from the classic form: predominance in children and young individuals, at a time of mild temperatures (spring), with no personal history of erythema pernio, collagenosis or other predisposing conditions. Then, EPL associated with COVID-19 was described. Since then, there have been numerous publications on the subject, including those showing the presence of the viral spike in skin lesions,1717 Colmenero I, Santonja C, Alonso-Ria˜no M, Noguera-Morel L,Hernández-Martín A, Andina D, et al. SARS-CoV-2 endothe-lial infection causes COVID-19 chilblains: histopathological,immunohistochemical and ultrastructural study of seven pae-diatric cases. Br J Dermatol. 2020;183:729-37. even in patients with a negative PCR result (swab). EPL is more frequent in healthy, oligo- or asymptomatic children and young adults with COVID-19, and it may be the only manifestation of the disease. Therefore, in the presence of these lesions, it is suggested that SARS-CoV-2 infection should be investigated. It appears on average after 10 to 14 days of the onset of general symptoms, lasts an average of 14 days, with spontaneous improvement.4141 Freeman EE, McMahon DE, Lipoff JB, Rosenbach M, Kovarik C, Takeshita J, et al. Pernio-like skin lesions associated with COVID-19: A case series of 318 patients from 8 countries. J Am Acad Dermatol. 2020;83:486-92. Most patients (in some series, up to 100% of them) have a negative PCR (swab) viral test result. This fact could be explained by the low viral load usually found in oligo- or asymptomatic COVID-19, in children, and in the later stages of the disease (10 to 14 days after symptoms onset). On the other hand, the absence of PCR positivity, therefore, of the laboratory confirmation of SARS-CoV-2 infection, raises the question of whether these patients were really infected. Immunohistochemistry and immunofluorescence studies may contribute to elucidating the relationship between EPL and COVID-19.4242 Kanitakis J, Lesort C, Danset M, Jullien D. Chilblain-like acral lesions during the COVID-19 pandemic (COVI¨ D toes¨): Histologic, immunofluorescence, and immunohistochemical study of 17 cases. J Am Acad Dermatol. 2020;83:870-5.

Recently, the relationship between EPL and SARS-CoV-2 infection has been widely questioned in the literature. One of the main controversies is precisely the lack of proof of SARS-CoV-2 infection in these patients. Case series of EPL have been published, which had no epidemiological, clinical, or laboratory evidence to support the diagnosis of COVID19,4343 Cleach LL, Dousset L, Assier H, Fourati S, Barbarot S, Boulard C, et al. Most chilblains observed during the COVID-19 outbreak occur in patients who are negative for COVID-19 on polymerase chain reaction and serology testing. Br J Dermatol. 2020;183:866-74. or even serological evidence, which could contribute to the pathophysiology of EPL.4444 Balestri R, Magnano M, Rizzoli L, Rech G. Do we have serological evidence that chilblain-like lesions are related to SARS-CoV-2? A review of the literature. Dermatol Ther. 2020;33:14229. Although the presence of the viral spike in EPL lesions has already been demonstrated by immunohistochemical techniques, and even the complete viral structure has been identified by electron microscopy, these were specific reports in the literature the vast majority of publications on EPL do not have this evidence. Regarding the pathophysiology, at the beginning of the pandemic, EPL, livedo, purpura, and necrosis lesions were interpreted as phases of the same spectrum of skin involvement. It is currently believed that they have distinct pathophysiological mechanisms.4545 Baeck M, Hoton D, Marot L, Herman A. Chilblains and COVID19: why SARS-CoV-2 endothelial infection is questioned. Br J Dermatol. 2020;183:1152-3.

Urticarial lesions

Infections, including viral ones, are known triggering factors for urticarial lesions. In this sense, SARS-CoV-2 infection could be a new triggering factor. Urticarial conditions associated with COVID-19 have been reported in patients without previous reports of the disease. A study in a private clinic reported an increased incidence of urticaria cases diagnosed during the pandemic, but no investigation was carried out regarding the presence of COVID-19 in these patients. Clinically, the lesions are disseminated, indistinguishable from other causes, and angioedema is rare. It is estimated that in 10% of patients, the skin condition may precede the general symptoms of COVID-19 by a few days, and, therefore, the detection of skin lesions could favor the early diagnosis of the infection. However, for the most part, urticarial lesions appear concomitantly with other symptoms. There is no age group predilection, and it is associated with mild systemic conditions with low mortality. Spontaneous improvement is reported within seven days or with the use of antihistamines and/or low-dose systemic corticosteroids.4646 Algaadi SA. Urticaria and COVID-19: A review. Dermatol Ther. 2020;33:14290.

Vesico-bullous eruptions

Although rare, vesico-bullous eruptions are considered a specific pattern of skin lesion associated with COVID-19, as they are not commonly seen in viral exanthem and drug reactions (main differential diagnoses). They consist of localized or disseminated vesicles or bullae (Fig. 2), which can affect the palmoplantar region, sparing mucous membranes. Their onset occurs approximately three days after the general symptoms and lasts for seven to 14 days, with spontaneous improvement and are associated with a mild to moderate systemic condition. In a series of cases, an attempt was made to isolate the viral agent from the bullous content using the PCR technique, without success. It is crucial to rule out other viral infections, especially herpetic ones, as a case of disseminated herpes with pneumonia has already been reported in a COVID-19 patient, showing the importance of the differential diagnosis.4747 Marzano AV, Genovese G, Fabbrocini G, Pigatto P, Monfrecola G, Piraccini BM, et al. Varicella-like exanthem as a specific COVID19-associated skin manifestation: Multicenter case series of 22 patients. J Am Acad Dermatol. 2020;83:280-5.

Figure 2
Vesico-bullous lesions in a patient with COVID-19.

Livedo, purpura, necrosis

The cutaneous vascular manifestations associated with COVID-19 comprise a wide spectrum, ranging from transient to fixed livedo reticularis, livedo racemosa, purpura, and necrosis of the extremities (Fig. 3). They are rare manifestations associated with severe systemic conditions, which occur late in elderly patients, those hospitalized in an intensive care environment, with multiple comorbidities and laboratory alterations (for example coagulopathies, elevated D-dimer levels). They are frequently associated with other thrombotic events such as deep vein thrombosis, ischemic stroke (cerebrovascular accident) and disseminated intravascular coagulation, which is responsible for the high mortality in this group. Therefore, skin findings in patients with a potentially fatal disease are very specific and distinct from those found in the outpatient profile. This happens because probably the same microangiopathic and thrombotic mechanisms occur simultaneously in the main target organs, such as the lung and kidneys, and in the skin.

Figure 3
Livedo racemosa, purpura and necrosis of the extremities in a patient with COVID-19.

Therefore, the treatment of skin lesions consists of treating the underlying disease itself.1616 Magro C, Mulvey JJ, Berlin D, Nuovo G, Salvatore S, Harp J, et al.Complement associated microvascular injury and thrombosis inthe pathogenesis of severe COVID-19 infection: A report of fivecases. Transl Res. 2020;220:1-13.,2222 Magro CM, Mulvey JJ, Laurence J, Sanders S, Crowson NA, Gross-man M, et al. The differing pathophysiologies that underlieCOVID-19-associated perniosis and thrombotic retiform pur-pura: a case series. Br J Dermatol. 2021;184:141-50.,2626 Casas CG, Català A, Hernández GC, Rodríguez-Jiménez P,Fernández-Nieto D, Lario ARV, et al. Classification of thecutaneous manifestations of COVID-19: a rapid prospectivenationwide consensus study in Spain with 375 cases. Br J Der-matol. 2020;183:71-7. A summary of the main characteristics of the dermatological manifestations described above is found in Table 4 (Main characteristics of the skin manifestations associated with COVID-19).

Table 4
Main characteristics of skin manifestations associated with COVID-19.

Other manifestations

Mucosal involvement

Oral lesions during the course of COVID-19 have also been described and collected in review articles. It is known that SARS-CoV-2 can be detected in saliva using the PCR technique, which is currently used for diagnostic purposes. Moreover, ACE2, a functional viral receptor in the body, is present in the oral mucosa, with greater density on the dorsum of the tongue and minor salivary glands, which would justify the presence of mucosal lesions. Dysgeusia was the first oral symptom recognized in COVID-19, with a widely varying frequency, from five to 88%. Subsequently, numerous oral lesions were also described, with the most frequent being enanthema, petechiae, aphthoid lesions or ulcers, herpetiform lesions, candidiasis, and oral lesions associated with Kawasaki disease. They are usually symptomatic (pain, burning sensation or pruritus) and appear four days before or up to 12 weeks after the general symptoms. The treatment depends on the pattern of the lesion identified. Inadequate oral hygiene, immunosuppression, reactivation of latent viruses (for example, herpes virus), opportunistic infections, stress, trauma secondary to intubation, COVID-19 hyperinflammatory response are predisposing factors. Further studies are required to define which oral manifestations are directly linked to SARS-CoV-2 infection and which are indirectly due to the presence of other mucosal affections that, in these cases, occur in the context of COVID-19. In this sense, research is essential to exclude such conditions. It is suggested that vascular alterations and microthrombusinduced manifestations, such as petechiae and ulcers and enanthema (similar to viral exanthem) may be directly associated with the pathophysiology of SARS-CoV-2.3434 Nuno-Gonzalez A, Martin-Carrillo P, Magaletsky K, Rios MDM,Ma˜nas CH, Almazan JA, et al. Prevalence of mucocutaneousmanifestations in 666 patients with COVID-19 in a field hos-pital in Spain: oral and palmoplantar findings. Br J Dermatol.2021;184:184-5.

35 Avancini J, Miyamoto D, Arnone M, Gabbi TVB, Ferreira PS, Festa-Neto C, et al. Absence of specific cutaneous manifestations of severe acute respiratory syndrome coronavirus 2 in a reference center in Brazil. J Am Acad Dermatol. 2021;84:67.

36 Jamshidi P, Hajikhani B, Mirsaeidi M, Vahidnezhad H, Dadashi M, Nasiri MJ. Skin Manifestations in COVID-19 Patients: Are They Indicators for Disease Severity? A Systematic Review. Front Med (Lausanne). 2021;8:634208.

37 Gisondi P, Leo SD, Bellinato F, Cazzaniga S, Piaserico S, Naldi L. Time of Onset of Selected Skin Lesions Associated with COVID-19: A Systematic Review. Dermatol Ther (Heidelb). 2021;11:695-705.

38 Mirza FN, Malik AA, Omer SB, Sethi A. Dermatologic manifestations of COVID-19: a comprehensive systematic review. Int J Dermatol. 2021;60:418-50.

39 Rosell-Díaz AM, Mateos-Mayo A, Nieto-Benito LM, BalaguerFranch I, Torre-Ruiz EH, Lainez-Nuez A, et al. Exanthem and eosinophilia in COVID-19 patients: has viral infection a role in drug induced exanthems? J Eur Acad Dermatol Venereol. 2020;34:561-3.

40 Fernandez-Nieto D, Jimenez-Cauhe J, Suarez-Valle A, MorenoArrones OM, Saceda-Corralo D, Arana-Raja A, et al. Characterization of acute acral skin lesions in nonhospitalized patients: A case series of 132 patients during the COVID-19 outbreak. J Am Acad Dermatol. 2020;83:61-3.

41 Freeman EE, McMahon DE, Lipoff JB, Rosenbach M, Kovarik C, Takeshita J, et al. Pernio-like skin lesions associated with COVID-19: A case series of 318 patients from 8 countries. J Am Acad Dermatol. 2020;83:486-92.

42 Kanitakis J, Lesort C, Danset M, Jullien D. Chilblain-like acral lesions during the COVID-19 pandemic (COVI¨ D toes¨): Histologic, immunofluorescence, and immunohistochemical study of 17 cases. J Am Acad Dermatol. 2020;83:870-5.

43 Cleach LL, Dousset L, Assier H, Fourati S, Barbarot S, Boulard C, et al. Most chilblains observed during the COVID-19 outbreak occur in patients who are negative for COVID-19 on polymerase chain reaction and serology testing. Br J Dermatol. 2020;183:866-74.

44 Balestri R, Magnano M, Rizzoli L, Rech G. Do we have serological evidence that chilblain-like lesions are related to SARS-CoV-2? A review of the literature. Dermatol Ther. 2020;33:14229.

45 Baeck M, Hoton D, Marot L, Herman A. Chilblains and COVID19: why SARS-CoV-2 endothelial infection is questioned. Br J Dermatol. 2020;183:1152-3.

46 Algaadi SA. Urticaria and COVID-19: A review. Dermatol Ther. 2020;33:14290.

47 Marzano AV, Genovese G, Fabbrocini G, Pigatto P, Monfrecola G, Piraccini BM, et al. Varicella-like exanthem as a specific COVID19-associated skin manifestation: Multicenter case series of 22 patients. J Am Acad Dermatol. 2020;83:280-5.
-4848 Iranmanesh B, Khalili M, Amiri R, Zartab H, Aflatoonian M. Oral manifestations of COVID-19 disease: A review article. Dermatol Ther. 2021;34:14578.

Telogen effluvium and COVID-19

Widely known in dermatology for a long time, telogen effluvium (TE) can be triggered by metabolic, nutritional changes, drug use, and several systemic conditions, including infections. In COVID-19, it is thought that the inflammatory cytokines released and the use of medications, such as heparin, may be involved in the TE mechanism. There is a report of an increase in the incidence of TE by almost threefold during the pandemic. It is estimated that 10% of patients with COVID-19 develop TE in the weeks and months following the infection, especially in patients with comorbidities, but it can occur even in subclinical conditions. To date, information about the onset, evolution, and prognosis of TE associated with COVID-19 are indistinguishable from TE due to other known causes. There is no peculiarity or specific characteristic in TE induced by SARSCoV-2 infection. Therefore, the approach, treatment, and follow-up of these patients should be the same adopted for TE in dermatological practice.4949 Moreno-Arrones OM, Lobato-Berezo A, Gomez-Zubiaur A, Arias-Santiago S, Saceda-Corralo D, Bernardez-Guerra C, et al. SARSCoV-2-induced telogen effluvium: a multicentric study. J Eur Acad Dermatol Venereol. 2021;35:181-3.,5050 Cline A, Jacobs AK, Fonseca M, Wu J, Asrani F, Safai B, et al. Race, ethnicity and comorbidities are critical factors in the diagnosis of telogen effluvium during the COVID-19 pandemic. J Am Acad Dermatol. 2021;85:209-11.

Case reports

In addition to the manifestations most often described and grouped into ‘‘patterns’’ in the large case series, prospective and systematic review studies, there are many isolated cases reports in the literature on several skin conditions possibly associated with COVID-19. Due to the methodological limitation inherent to case report-type publications, the actual role of SARS-CoV-2 infection in these entities cannot be affirmed, that is, whether they are in fact attributable to COVID-19 or not. The isolated conditions associated with COVID-19 that have been published in case reports are shown in Table 5 (Dermatological conditions associated with COVID19 - Case reports).

Table 5
Dermatological conditions associated with COVID-19 - Case reports.

The first reports were of cases of urticaria, which even preceded clinical symptoms,5151 Quintana-Castanedo L, Feito-Rodríguez M, Valero-López I, Chiloeches-Fernández C, Sendagorta-Cudós E, Herranz-Pinto P. Urticarial exanthem as early diagnostic clue for COVID-19 infection. JAAD Case Rep. 2020;6:498-9. urticarial vasculitis,5252 Perosanz-Lobo D, Fernandez-Nieto D, Burgos-Blasco P, SeldaEnriquez G, Carretero I, Moreno C, et al. Urticarial vasculitis in COVID-19 infection: a vasculopathy-related symptom? J Eur Acad Dermatol Venereol. 2020;34:566-8. and angioedema.5353 Elhag SAA, Ibrahim H, Abdelhadi S. Angioedema and urticaria in a COVID-19 patient: A case report and review of the literature. JAAD Case Rep. 2020;6:1091-4. Also, cases of pityriasis rosea or pityriasis rosea-like lesions,5454 Johansen M, Chisolm SS, Aspey LD, Brahmbhatt M. Pityriasis rosea in otherwise asymptomatic confirmed COVID-19-positive patients: A report of 2 cases. JAAD Case Rep. 2021;7:93-4. with one report showing the presence of SARS-CoV-2 by immunohistochemical techniques5555 Welsh E, Garza JAC, Cuellar-Barboza A, Franco-Marquez R, Arvizu-Rivera RI. SARS-CoV-2 spike protein positivity in pityriasis rosea-like and urticaria-like rashes of COVID-19. Br J Dermatol. 2021;184:1194-5. and another pointing to the possible role of HHV-6 reactivation and other viruses in these cases.5656 Dursun R, Temiz SA. The clinics of HHV-6 infection in COVID19 pandemic: Pityriasis rosea and Kawasaki disease. Dermatol Ther. 2020;33:13730.

There have also been reports of small-vessel vasculitis associated with COVID-19,5757 Tahir A, Sohail Z, Nasim B, Parmar NV. Widespread cutaneous small vessel vasculitis secondary to COVID-19 infection. Int J Dermatol. 2020;59:1278-9. leukocytoclastic vasculitis,5858 Gómez MC, González-Cruz C, Ferrer B, Barberá MJ. Leucocytoclastic vasculitis in a patient with COVID-19 with positive SARS-CoV-2 PCR in skin biopsy. BMJ Case Rep. 2020;13:238039. IgA vasculitis,5959 Sandhu S, Chand S, Bhatnagar A, Dabas R, Bhat S, Kumar H, et al. Possible association between IgA vasculitis and COVID-19. Dermatol Ther. 2021;34:14551. granulomatosis with polyangiitis (formerly called Wegener’s disease),6060 Bressler MY, Pathak N, Cervellione K, Bagheri F, Epstein E, Mir A, et al. New Onset Granulomatosis with Polyangiitis Associated with COVID-19. Case Rep Dermatol Med. 2021;2021:8877292. eosinophilic granulomatosis with polyangiitis (formerly called Churg-Strauss syndrome),6161 Hashizume H, Sano Y, Furukawa S, Imokawa S. Eosinophilic granulomatosis with polyangiitis mimicking coronavirus disease 2019: a case report. J Eur Acad Dermatol Venereol. 2020;34:557-9. Schamberg purpura6262 Wollina U. Schamberg-like purpuric eruptions and tonsillitis in mild COVID-19. Dermatol Ther. 2020;33:13766. and purpura fulminans.6363 Khan IA, Karmakar S, Chakraborty U, Sil A, Chandra A. Purpura fulminans as the presenting manifestation of COVID-19. Postgrad Med J. 2021;97:473.

Regarding conditions that resemble drug reactions, patients with COVID-19 and erythema multiforme have been described,6464 Janah H, Zinebi A, Elbenaye J. Atypical erythema multiforme palmar plaques lesions due to Sars-Cov-2. J Eur Acad Dermatol Venereol. 2020;34:373-5. as well as case series of acute generalized exanthematous pustulosis (AGEP),6565 Pezzarossa E, Ungari M, Caresana G, Sagradi F, Cimardi L, Pan A, et al. Acute Generalized Exanthemtous Pustulosis (AGEP) in 12 Patients Treated for SARS-CoV-2 Positive Pneumonia. Am J Dermatopathol. 2021;43:342-8. reports of toxic epidermal necrolysis (TEN)6666 Tanaka A, Isei M, Kikuzawa C, Hinogami H, Nishida K, Gohma I, et al. Development of toxic epidermal necrolysis in a coronavirus disease 2019 patient with recurrence of positive SARS-CoV-2 viral RNA. J Dermatol. 2021;48:144-5. and SDRIFE (symmetrical drug-related intertriginous and flexural exanthem).6767 Chicharro P, Rodríguez-Jiménez P, Munoz-Aceitun˜ o E, Argila D, Munoz-Hernánde˜ z P, Llamas-Velasco M. SDRIFE-like rash associated with COVID-19, clinicopathological correlation. Australas J Dermatol. 2021;62:88-9.

There are also case reports in specific topographies - ungual involvement, with a description of the ‘‘red half-moon sign’’6868 Neri I, Guglielmo A, Virdi A, Gaspari V, Starace M, Piraccini BM. The red half-moon nail sign: a novel manifestation of coronavirus infection. J Eur Acad Dermatol Venereol. 2020;34:663-5.; palmoplantar involvement with erythrodysesthesia6969 Nuno-Gonzalez A, Magaletsky K, Rodríguez FM, Ibarguren AM, Beato MJ, Bravo ER, et al. Palmoplantar erythrodysesthesia: a diagnostic sign of COVID-19. J Eur Acad Dermatol Venereol. 2021;35:247-9.; follicular eruption,7070 Danarti R, Budiarso A, Rini DLU, Soebono H. Follicular eruption as a cutaneous manifestation in COVID-19. BMJ Case Rep. 2020;13:238182. unilateral exanthem,7171 Glick LR, Fogel AL, Ramachandran S, Barakat LA. Unilateral laterothoracic exanthem in association with coronavirus disease 2019. JAAD Case Rep. 2020;6:900-1. unilateral livedo reticularis7272 Tusheva I, Damevska K, Dimitrovska I, Markovska Z, MalinovskaNikolovska L. Unilateral livedo reticularis in a COVID-19 patient: Case with fatal outcome. JAAD Case Rep. 2021;7:120-1. and pressure ulcers in unusual locations (such as the sternum, knees) from prolonged pronation.7373 Ramondetta A, Ribero S, Costi S, Dapavo P. Pression-induced facial ulcers by prone position for COVID-19 mechanical ventilation. Dermatol Ther. 2020;33:13748. Dermoscopic descriptions of purpuric papular eruption7474 Larrondo J, Cabrera R, Gosch M, Larrondo F, Aylwin M, Castro A. Papular-purpuric exanthem in a COVID-19 patient: clinical and dermoscopic description. J Eur Acad Dermatol Venereol. 2020;34:570-2. and EPL lesions have been published.7575 Piccolo V, Bassi A, Argenziano G, Mazzatenta G, Guglielmo A, Patrizi A, et al. Dermoscopy of chilblain-like lesions during the COVID-19 outbreak: A multicenter study on 10 patients. J Am Acad Dermatol. 2020;83:1749-51.

There are also reports of herpes zoster7676 Nofal A, Fawzy MM, Deen SMS, El-Hawary EE. Herpes zoster ophthalmicus in COVID-19 patients. Int J Dermatol. 2020;59:1545-6. and isolated reports of Grover’s disease-like conditions,7777 Boix-Vilanova J, Gracia-Darder I, Saus C, Ramos D, Llull A, Santonja C, et al. Grover-like skin eruption: another cutaneous manifestation in a COVID-19 patient. Int J Dermatol. 2020;59:1290-2. Melkersson-Rosenthal syndrome,7878 Taşlıdere B, Mehmetaj L, Özcan AB, Gülen B, Taşlıdere N. Melkersson-Rosenthal Syndrome Induced by COVID-19. Am J Emerg Med. 2021;41:262. erythema nodosum,7979 Sipfle N, Bridwell RE, Roper J. Erythema nodosum-like rash in a COVID-19 patient: A case report. Am J Emerg Med. 2021;40:227. sarcoid lesion,8080 Behbahani S, Baltz JO, Droms R, Deng AC, Amano SU, Levin NA, et al. Sarcoid-like reaction in a patient recovering from coronavirus disease 19 pneumonia. JAAD Case Rep. 2020;6:915-7. Gianotti-Crosti syndrome,8181 Brin C, Sohier P, L’honneur AS, Marot S, Matar S, Aractingi S, et al. An Isolated Peculiar Gianotti-Crosti Rash in the Course of a COVID-19 Episode. Acta Derm Venereol. 2020;100:00276. seborrheic dermatitis,8282 Alpalhão M, Gaibino N, Filipe P. Seborrheic dermatitis in COVID19: a case report. Int J Dermatol. 2020;59:1543-4. annular lichen planus,8383 Diaz-Guimaraens B, Dominguez-Santas M, Suarez-Valle A, Fernandez-Nieto D, Jimenez-Cauhe J, Ballester A. Annular lichen planus associated with coronavirus SARS-CoV-2 disease (COVID-19). Int J Dermatol. 2021;60:246-7. erythema annulare centrifugum,8484 Montinari M, Atzori L, Valdevit S, Rongioletti F. Erythema annulare centrifugum with anosmia and ageusia in a SARS-CoV-2 exposed patient successfully treated with doxycycline. Int J Dermatol. 2021;60:384-6. granuloma annulare8585 Monte-Serrano J, García-Gil MF, García-García M, Casas-Flecha I, Matovelle-Ochoa C, Ara-Martín M, et al. Granuloma annulare triggered by SARS-CoV-2 infection: Immunohistochemical staining. Dermatol Ther. 2021;34:14897. and rapidly progressive alopecia areata.8686 FIvenson D. COVID-19: association with rapidly progressive forms of alopecia areata. Int J Dermatol. 2021;60:127.

Histopathology of skin manifestations of COVID-19

Some studies presented the first descriptions of histopathological and immunohistochemical changes in skin lesions associated with COVID-19, aiming to contribute to the understanding of the pathophysiological mechanisms of these manifestations. The main histopathological changes of the most often described skin patterns will be briefly mentioned below.8787 Kaya G, Kaya A, Saurat JH. Clinical and Histopathological Features and Potential Pathological Mechanisms of Skin Lesions in COVID-19: Review of the Literature. Dermatopathology (Basel). 2020;7:3-16.

Maculopapular eruptions

Superficial perivascular dermatitis with mild lymphocytosis, thrombosed vessels with neutrophilic and eosinophilic debris; interface dermatitis, superficial and deep perivascular lymphocytic infiltrate, with or without vasculitis (Fig. 4).

Figure 4
Histopathological findings of exanthem in a patient with COVID-19. (A), Leukocytoclastic vasculitis in the capillary vessels of the superficial dermis and erythrodiapedesis (Hematoxylin & eosin, ×100). (B), Capillary vessels containing intact and degenerated neutrophils partially destroying the wall, extravasated red blood cells, and the presence of eosinophilic amorphous material in the vascular lumen, suggestive of fibrin thrombus (Hematoxylin & eosin, ×400).

Erythema pernio-like (EPL)

In the epidermis, presence of parakeratosis and hyperkeratosis, with apoptotic keratinocytes and, eventually, epidermal necrosis. Dense lymphocytic infiltrate in the superficial and deep dermis, also in the hypodermis, with a perivascular pattern and signs of endothelial activation. Sometimes, eccrine lymphocytic infiltrate is similar to that seen in eccrine lymphocytic hidradenitis. Other common findings are erythrodiapedesis, edema in the papillary dermis with the formation of a subepidermal bulla and increased interstitial mucin deposition. The presence of vascular microthrombi in the capillaries of the superficial dermis is rare, a well as in dermal venules.

Urticarial eruptions

Perivascular lymphocytic infiltrate with some eosinophils and edema in the superficial dermis, eventually with vacuolar interface dermatitis and keratinocyte necrosis, with a pattern similar to that of erythema multiforme. In urticarial vasculitis, there is extravasation of red blood cells with perivascular neutrophilic infiltrate, macrophages, necrosis, and fibrin deposits.

Vesicular eruptions

Acanthosis, vesicles due to vacuolar degeneration of the basal layer with dyskeratotic, multinucleated cells (suggestive of viral inclusion) without inflammatory infiltrate. In these cases, the differential diagnosis with herpetic dermatoviruses is essential.

Livedo, purpura

Thrombotic vasculopathy with extensive deposition of C5b-9 and C4d (immunohistochemical technique) in the microvasculature.

Androgens and COVID-19

Throughout the pandemic, SARS-CoV-2 infection was observed to affect more men than women. Men are twice as likely to be admitted to intensive care units. The association between the androgen pathway and SARS-CoV-2 infectivity has been described. Therefore, such predisposition to androgen-mediated infection could justify the high rates of hospitalization and mortality concentrated in men. Therefore, androgen expression in the form of alopecia (androgenetic alopecia - AGA) could, by itself, be a risk factor for COVID-19, and a high frequency of AGA has been reported among hospitalized men; and also the use of antiandrogens could be a protective and/or therapeutic factor in the evolution of these patients. In this sense, a published study showed that men with AGA or benign prostatic hyperplasia using a 5-alpha-reductase inhibitor who contracted COVID-19 showed a significant reduction in symptoms in the outpatient setting. In a case-control study in a hospital setting, men using 5-alpha-reductase inhibitors had a lower chance of being admitted to the ICU (Intensive Care Unit), suggesting this protective effect. However, it is still uncertain whether the introduction of anti-androgens after SARS-CoV-2 infection would provide any benefit. Apparently, dermatologists should encourage their AGA patients to maintain anti-androgen use during the pandemic. This is undoubtedly a very promising field of research.8888 Wambier CG, Goren A. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is likely to be androgen mediated. J Am Acad Dermatol. 2020;83:308-9.

89 Goren A, Wambier CG, Herrera S, McCoy J, Vano-Galvᘠn S, Gioia F, et al. Anti-androgens may protect against severe COVID-19 outcomes: results from a prospective cohort study of 77 hospitalized men. J Eur Acad Dermatol Venereol. 2021;35:13-5.
-9090 McCoy J, Cadegiani FA, Wambier CG, Herrera S, Vano-Galvᘠn S, Mesinkovska NA, et al. 5-alpha-reductase inhibitors are associated with reduced frequency of COVID-19 symptoms in males with androgenetic alopecia. J Eur Acad Dermatol Venereol. 2021;35:243-6.

Final considerations

Although the number of publications in a short period of time is significant and growing, there are still many challenging questions about the skin manifestations associated with COVID-19. The actual frequency of cutaneous findings is widely variable (0.2% to 45%) in the literature, and systematic review studies point to a frequency close to 6%. The most common dermatological manifestations were maculopapular eruptions, followed by EPL lesions. However, some publications mention that EPL lesions are the most prevalent manifestations. Urticarial, vesicular and livedo eruptions, in addition to purpura and necrosis, are less often described. As for the time of onset, skin lesions usually occur concomitantly with general symptoms and can rarely precede them, as in cases of urticaria and vesicular lesions. EPL can appear late or even be the only clinical manifestation of COVID-19. Vascular conditions such as livedo, purpura and necrosis are equally late manifestations but associated with greater severity and worse prognosis. Histopathological and immunohistochemical studies of the different patterns of skin lesions in patients with COVID-19 are essential for a better understanding of their pathophysiological significance in relation to the disease (are they directly caused by the viral infection? resulting from complications of systemic disease?).

It is worth emphasizing the importance of ruling out possible differential diagnoses in a patient with COVID-19 who presents skin lesions before attributing the skin condition exclusively to the viral infection. Spontaneous urticaria, other viral infections, drug reactions, among others, should be considered when investigating these patients.

The contribution of Dermatology to the COVID-19 pandemic seems to go beyond skin manifestations. The close relationship between androgens and the course of SARSCoV-2 infection opens up a promising field of research on their prognostic and protective effects, especially regarding the systemic use of anti-androgens, widely prescribed in dermatology.

The pandemic has provided an excellent opportunity for dermatologists to learn and contribute. Unfortunately, it is not over yet. As science is a dynamic process, there is hope that more studies will be carried out so that answers can be found and uncertainties can be resolved.

  • Financial support
    None declared.

References

  • 1
    Shinkai K, Bruckner AL. Dermatology and COVID-19. JAMA.2020;324:1133-4.
  • 2
    Joob B, Wiwanitkit V. COVID-19 can present with a rash and bemistaken for dengue. J Am Acad Dermatol. 2020;82:177.
  • 3
    Guan WJ, Ni ZY, Hu Y, Liang WH, Ou CQ, He JX, et al. ClinicalCharacteristics of Coronavirus Disease 2019 in China. N Engl JMed. 2020;382:1708-20.
  • 4
    Recalcati S. Cutaneous manifestations in COVID-19: a first per-spective. J Eur Acad Dermatol Venereol. 2020;34:212-3.
  • 5
    Matar S, Oulès B, Sohier P, Chosidow O, Beylot-Barroy M, Dupin N, et al. Cutaneous manifestations in SARS-CoV-2 infection(COVID-19): a French experience and a systematic review ofthe literature. J Eur Acad Dermatol Venereol. 2020;34:686-9.
  • 6
    Rerknimitr P, Theerawattanawit C, Lertpichitkul P, Jan-tarabenjakul W, Putcharoen O, Puthanakit T, et al. Skinmanifestations in COVID-19: The tropics experience. J Derma-tol. 2020;47:444-6.
  • 7
    Solak EO, Ketencioglu BB, Aslaner H, Çinar SL, Kartal D, Benli AR, et al. Cutaneous symptoms of patients diagnosed withCOVID-19 in one province: a cross-sectional survey. J Eur AcadDermatol Venereol. 2021;35:105-6.
  • 8
    Gaspari V, Orioni G, Misciali C, Viviani F, Zengarini C. COVID-19skin eruptions: incidence in hospitalized patients in Bologna. IntJ Dermatol. 2021;60:512-3.
  • 9
    Tammaro A, Adebanjo GAR, Parisella FR, Pezzuto A, RelloJ. Cutaneous manifestations in COVID-19: the experiencesof Barcelona and Rome. J Eur Acad Dermatol Venereol.2020;34:306-7.
  • 10
    Tamai M, Maekawa A, Goto N, Ge L, Nishida T, Iwahashi H, et al.Three cases of COVID-19 patients presenting with erythema. JDermatol. 2020;47:1175-8.
  • 11
    Fernandez-Guarino M, Ortega-Quijano D, Suarez-Valle A,Jimenez-Cauhe J, Jaen-Olasolo P, Fernandez-Guarino M, et al.Lack of skin manifestations in COVID-19 hospitalized patientsduring the second epidemic wave in Spain: a possible associa-tion with a novel SARS-CoV-2 variant a cross sectional study. JEur Acad Dermatol Venereol. 2021;35:183-5.
  • 12
    Criado PR, Pincelli TPH, Criado RFJ, Abdalla BMZ, Belda JuniorW. Potential interactions of SARS-CoV-2 with human cell recep-tors in the skin: Understanding the enigma for a lower frequencyof skin lesions compared to other tissues. Exp Dermatol.2020;29:936-44.
  • 13
    Unterluggauer L, Pospischil I, Krall C, Saluzzo S, Kimeswenger S,Karolyi M, et al. Cutaneous manifestations of SARS-CoV-2 a two-center, prospective, case-controlled study. J Am Acad Dermatol.2021;85:202-4.
  • 14
    Bourgonje AR, Abdulle AE, Timens W, Hillebrands JL, Navis GJ, Gordijn SJ, et al. Angiotensin-converting enzyme 2 (ACE2),SARS-CoV-2 and the pathophysiology of coronavirus disease 2019(COVID-19). J Pathol. 2020;251:228-48.
  • 15
    Jamiolkowski D, Mühleisen B, Müller S, Navarini AA, Tzankov A,Roider E. SARS-CoV-2 PCR testing of skin for COVID-19 diagnos-tics: a case report. Lancet. 2020;396:598-9.
  • 16
    Magro C, Mulvey JJ, Berlin D, Nuovo G, Salvatore S, Harp J, et al.Complement associated microvascular injury and thrombosis inthe pathogenesis of severe COVID-19 infection: A report of fivecases. Transl Res. 2020;220:1-13.
  • 17
    Colmenero I, Santonja C, Alonso-Ria˜no M, Noguera-Morel L,Hernández-Martín A, Andina D, et al. SARS-CoV-2 endothe-lial infection causes COVID-19 chilblains: histopathological,immunohistochemical and ultrastructural study of seven pae-diatric cases. Br J Dermatol. 2020;183:729-37.
  • 18
    Criado PR, Abdalla BMZ, Assis IC, Mello CBG, Caputo GC, VieiraIC. Are the cutaneous manifestations during or due to SARS-CoV-2 infection/COVID-19 frequent or not? Revision of possiblepathophysiologic mechanisms. Inflamm Res. 2020;69:745-56.
  • 19
    Suchonwanit P, Leerunyakul K, Kositkuljorn C. Cutaneous mani-festations in COVID-19: Lessons learned from current evidence.J Am Acad Dermatol. 2020;83:57-60.
  • 20
    Criado PR, Pagliari C, Carneiro FRO, Quaresma JAS. Lessonsfrom dermatology about inflammatory responses in Covid-19.Rev Med Virol. 2020;30:2130.
  • 21
    Cavanagh G, Criado PR, Pagliari C, Carneiro FRO, Quaresma JAS,Cappel MA, et al. Pernio during the COVID-19 pandemic andreview of inflammation patterns and mechanisms of hypercoag-ulability. JAAD Case Rep. 2020;6:898-9.
  • 22
    Magro CM, Mulvey JJ, Laurence J, Sanders S, Crowson NA, Gross-man M, et al. The differing pathophysiologies that underlieCOVID-19-associated perniosis and thrombotic retiform pur-pura: a case series. Br J Dermatol. 2021;184:141-50.
  • 23
    Santonja C, Heras F, Nú˜nez L, Requena L. COVID-19 chilblain-like lesion: immunohistochemical demonstration of SARS-CoV-2 spike protein in blood vessel endothelium and sweat glandepithelium in a polymerase chain reaction-negative patient. BrJ Dermatol. 2020;183:778-80.
  • 24
    García-Gil MF, Monte-Serrano J, García MG, Prieto-Torres L,Pascual-Del-Riquelme AJ, Flecha IC, et al. Absence of SARS-CoV-2 RNA detection in tissue samples of COVID-19-relatedcutaneous lesions analyzed by real-time RT-PCR. J Eur AcadDermatol Venereol. 2021;35:318-21.
  • 25
    Abadías-Granado I, Navarro-Bielsa A, Morales-Callaghan AM,Roc L, Suso-Estívalez CC, Povar-Echeverría M, et al. COVID-19-associated cutaneous manifestations: does human herpesvirus6 play an aetiological role? Br J Dermatol. 2021;184:1187-90.
  • 26
    Casas CG, Català A, Hernández GC, Rodríguez-Jiménez P,Fernández-Nieto D, Lario ARV, et al. Classification of thecutaneous manifestations of COVID-19: a rapid prospectivenationwide consensus study in Spain with 375 cases. Br J Der-matol. 2020;183:71-7.
  • 27
    Masson A, Bouaziz JD, Sulimovic L, Cassius C, Jachiet M, Ionescu MA, et al. Chilblains is a common cutaneous finding duringthe COVID-19 pandemic: A retrospective nationwide study fromFrance. J Am Acad Dermatol. 2020;83:667-70.
  • 28
    Freeman EE, McMahon DE, Lipoff JB, Rosenbach M, Kovarik C,Desai SR, et al. The spectrum of COVID-19-associated dermato-logic manifestations: An international registry of 716 patientsfrom 31 countries. J Am Acad Dermatol. 2020;83:1118-29.
  • 29
    Marzano AV, Genovese G, Moltrasio C, Gaspari V, Vezzoli P,Maione V, et al. The clinical spectrum of COVID-19-associatedcutaneous manifestations: An Italian multicenter study of 200adult patients. J Am Acad Dermatol. 2021;84:1356-63.
  • 30
    Visconti A, Bataille V, Rossi N, Kluk J, Murphy R, Puig S, et al.Diagnostic value of cutaneous manifestation of SARS-CoV-2infection. Br J Dermatol. 2021;184:880-7.
  • 31
    De Giorgi V, Recalcati S, Jia Z, Chong W, Ding R, Deng Y, et al.Cutaneous manifestations related to coronavirus disease 2019(COVID-19): A prospective study from China and Italy. J Am AcadDermatol. 2020;83:674-5.
  • 32
    Rekhtman S, Tannenbaum R, Strunk A, Birabaharan M, Wright S, Grbic N, et al. Eruptions and related clinical course among296 hospitalized adults with confirmed COVID-19. J Am AcadDermatol. 2021;84:946-52.
  • 33
    Maestro IM, Merino LP, Tánago BUG, González AA, Sope˜na AO,Vicente JS, et al. Skin manifestations in patients hospitalizedwith confirmed COVID-19 disease: a cross-sectional study in atertiary hospital. Int J Dermatol. 2020;59:1353-7.
  • 34
    Nuno-Gonzalez A, Martin-Carrillo P, Magaletsky K, Rios MDM,Ma˜nas CH, Almazan JA, et al. Prevalence of mucocutaneousmanifestations in 666 patients with COVID-19 in a field hos-pital in Spain: oral and palmoplantar findings. Br J Dermatol.2021;184:184-5.
  • 35
    Avancini J, Miyamoto D, Arnone M, Gabbi TVB, Ferreira PS, Festa-Neto C, et al. Absence of specific cutaneous manifestations of severe acute respiratory syndrome coronavirus 2 in a reference center in Brazil. J Am Acad Dermatol. 2021;84:67.
  • 36
    Jamshidi P, Hajikhani B, Mirsaeidi M, Vahidnezhad H, Dadashi M, Nasiri MJ. Skin Manifestations in COVID-19 Patients: Are They Indicators for Disease Severity? A Systematic Review. Front Med (Lausanne). 2021;8:634208.
  • 37
    Gisondi P, Leo SD, Bellinato F, Cazzaniga S, Piaserico S, Naldi L. Time of Onset of Selected Skin Lesions Associated with COVID-19: A Systematic Review. Dermatol Ther (Heidelb). 2021;11:695-705.
  • 38
    Mirza FN, Malik AA, Omer SB, Sethi A. Dermatologic manifestations of COVID-19: a comprehensive systematic review. Int J Dermatol. 2021;60:418-50.
  • 39
    Rosell-Díaz AM, Mateos-Mayo A, Nieto-Benito LM, BalaguerFranch I, Torre-Ruiz EH, Lainez-Nuez A, et al. Exanthem and eosinophilia in COVID-19 patients: has viral infection a role in drug induced exanthems? J Eur Acad Dermatol Venereol. 2020;34:561-3.
  • 40
    Fernandez-Nieto D, Jimenez-Cauhe J, Suarez-Valle A, MorenoArrones OM, Saceda-Corralo D, Arana-Raja A, et al. Characterization of acute acral skin lesions in nonhospitalized patients: A case series of 132 patients during the COVID-19 outbreak. J Am Acad Dermatol. 2020;83:61-3.
  • 41
    Freeman EE, McMahon DE, Lipoff JB, Rosenbach M, Kovarik C, Takeshita J, et al. Pernio-like skin lesions associated with COVID-19: A case series of 318 patients from 8 countries. J Am Acad Dermatol. 2020;83:486-92.
  • 42
    Kanitakis J, Lesort C, Danset M, Jullien D. Chilblain-like acral lesions during the COVID-19 pandemic (COVI¨ D toes¨): Histologic, immunofluorescence, and immunohistochemical study of 17 cases. J Am Acad Dermatol. 2020;83:870-5.
  • 43
    Cleach LL, Dousset L, Assier H, Fourati S, Barbarot S, Boulard C, et al. Most chilblains observed during the COVID-19 outbreak occur in patients who are negative for COVID-19 on polymerase chain reaction and serology testing. Br J Dermatol. 2020;183:866-74.
  • 44
    Balestri R, Magnano M, Rizzoli L, Rech G. Do we have serological evidence that chilblain-like lesions are related to SARS-CoV-2? A review of the literature. Dermatol Ther. 2020;33:14229.
  • 45
    Baeck M, Hoton D, Marot L, Herman A. Chilblains and COVID19: why SARS-CoV-2 endothelial infection is questioned. Br J Dermatol. 2020;183:1152-3.
  • 46
    Algaadi SA. Urticaria and COVID-19: A review. Dermatol Ther. 2020;33:14290.
  • 47
    Marzano AV, Genovese G, Fabbrocini G, Pigatto P, Monfrecola G, Piraccini BM, et al. Varicella-like exanthem as a specific COVID19-associated skin manifestation: Multicenter case series of 22 patients. J Am Acad Dermatol. 2020;83:280-5.
  • 48
    Iranmanesh B, Khalili M, Amiri R, Zartab H, Aflatoonian M. Oral manifestations of COVID-19 disease: A review article. Dermatol Ther. 2021;34:14578.
  • 49
    Moreno-Arrones OM, Lobato-Berezo A, Gomez-Zubiaur A, Arias-Santiago S, Saceda-Corralo D, Bernardez-Guerra C, et al. SARSCoV-2-induced telogen effluvium: a multicentric study. J Eur Acad Dermatol Venereol. 2021;35:181-3.
  • 50
    Cline A, Jacobs AK, Fonseca M, Wu J, Asrani F, Safai B, et al. Race, ethnicity and comorbidities are critical factors in the diagnosis of telogen effluvium during the COVID-19 pandemic. J Am Acad Dermatol. 2021;85:209-11.
  • 51
    Quintana-Castanedo L, Feito-Rodríguez M, Valero-López I, Chiloeches-Fernández C, Sendagorta-Cudós E, Herranz-Pinto P. Urticarial exanthem as early diagnostic clue for COVID-19 infection. JAAD Case Rep. 2020;6:498-9.
  • 52
    Perosanz-Lobo D, Fernandez-Nieto D, Burgos-Blasco P, SeldaEnriquez G, Carretero I, Moreno C, et al. Urticarial vasculitis in COVID-19 infection: a vasculopathy-related symptom? J Eur Acad Dermatol Venereol. 2020;34:566-8.
  • 53
    Elhag SAA, Ibrahim H, Abdelhadi S. Angioedema and urticaria in a COVID-19 patient: A case report and review of the literature. JAAD Case Rep. 2020;6:1091-4.
  • 54
    Johansen M, Chisolm SS, Aspey LD, Brahmbhatt M. Pityriasis rosea in otherwise asymptomatic confirmed COVID-19-positive patients: A report of 2 cases. JAAD Case Rep. 2021;7:93-4.
  • 55
    Welsh E, Garza JAC, Cuellar-Barboza A, Franco-Marquez R, Arvizu-Rivera RI. SARS-CoV-2 spike protein positivity in pityriasis rosea-like and urticaria-like rashes of COVID-19. Br J Dermatol. 2021;184:1194-5.
  • 56
    Dursun R, Temiz SA. The clinics of HHV-6 infection in COVID19 pandemic: Pityriasis rosea and Kawasaki disease. Dermatol Ther. 2020;33:13730.
  • 57
    Tahir A, Sohail Z, Nasim B, Parmar NV. Widespread cutaneous small vessel vasculitis secondary to COVID-19 infection. Int J Dermatol. 2020;59:1278-9.
  • 58
    Gómez MC, González-Cruz C, Ferrer B, Barberá MJ. Leucocytoclastic vasculitis in a patient with COVID-19 with positive SARS-CoV-2 PCR in skin biopsy. BMJ Case Rep. 2020;13:238039.
  • 59
    Sandhu S, Chand S, Bhatnagar A, Dabas R, Bhat S, Kumar H, et al. Possible association between IgA vasculitis and COVID-19. Dermatol Ther. 2021;34:14551.
  • 60
    Bressler MY, Pathak N, Cervellione K, Bagheri F, Epstein E, Mir A, et al. New Onset Granulomatosis with Polyangiitis Associated with COVID-19. Case Rep Dermatol Med. 2021;2021:8877292.
  • 61
    Hashizume H, Sano Y, Furukawa S, Imokawa S. Eosinophilic granulomatosis with polyangiitis mimicking coronavirus disease 2019: a case report. J Eur Acad Dermatol Venereol. 2020;34:557-9.
  • 62
    Wollina U. Schamberg-like purpuric eruptions and tonsillitis in mild COVID-19. Dermatol Ther. 2020;33:13766.
  • 63
    Khan IA, Karmakar S, Chakraborty U, Sil A, Chandra A. Purpura fulminans as the presenting manifestation of COVID-19. Postgrad Med J. 2021;97:473.
  • 64
    Janah H, Zinebi A, Elbenaye J. Atypical erythema multiforme palmar plaques lesions due to Sars-Cov-2. J Eur Acad Dermatol Venereol. 2020;34:373-5.
  • 65
    Pezzarossa E, Ungari M, Caresana G, Sagradi F, Cimardi L, Pan A, et al. Acute Generalized Exanthemtous Pustulosis (AGEP) in 12 Patients Treated for SARS-CoV-2 Positive Pneumonia. Am J Dermatopathol. 2021;43:342-8.
  • 66
    Tanaka A, Isei M, Kikuzawa C, Hinogami H, Nishida K, Gohma I, et al. Development of toxic epidermal necrolysis in a coronavirus disease 2019 patient with recurrence of positive SARS-CoV-2 viral RNA. J Dermatol. 2021;48:144-5.
  • 67
    Chicharro P, Rodríguez-Jiménez P, Munoz-Aceitun˜ o E, Argila D, Munoz-Hernánde˜ z P, Llamas-Velasco M. SDRIFE-like rash associated with COVID-19, clinicopathological correlation. Australas J Dermatol. 2021;62:88-9.
  • 68
    Neri I, Guglielmo A, Virdi A, Gaspari V, Starace M, Piraccini BM. The red half-moon nail sign: a novel manifestation of coronavirus infection. J Eur Acad Dermatol Venereol. 2020;34:663-5.
  • 69
    Nuno-Gonzalez A, Magaletsky K, Rodríguez FM, Ibarguren AM, Beato MJ, Bravo ER, et al. Palmoplantar erythrodysesthesia: a diagnostic sign of COVID-19. J Eur Acad Dermatol Venereol. 2021;35:247-9.
  • 70
    Danarti R, Budiarso A, Rini DLU, Soebono H. Follicular eruption as a cutaneous manifestation in COVID-19. BMJ Case Rep. 2020;13:238182.
  • 71
    Glick LR, Fogel AL, Ramachandran S, Barakat LA. Unilateral laterothoracic exanthem in association with coronavirus disease 2019. JAAD Case Rep. 2020;6:900-1.
  • 72
    Tusheva I, Damevska K, Dimitrovska I, Markovska Z, MalinovskaNikolovska L. Unilateral livedo reticularis in a COVID-19 patient: Case with fatal outcome. JAAD Case Rep. 2021;7:120-1.
  • 73
    Ramondetta A, Ribero S, Costi S, Dapavo P. Pression-induced facial ulcers by prone position for COVID-19 mechanical ventilation. Dermatol Ther. 2020;33:13748.
  • 74
    Larrondo J, Cabrera R, Gosch M, Larrondo F, Aylwin M, Castro A. Papular-purpuric exanthem in a COVID-19 patient: clinical and dermoscopic description. J Eur Acad Dermatol Venereol. 2020;34:570-2.
  • 75
    Piccolo V, Bassi A, Argenziano G, Mazzatenta G, Guglielmo A, Patrizi A, et al. Dermoscopy of chilblain-like lesions during the COVID-19 outbreak: A multicenter study on 10 patients. J Am Acad Dermatol. 2020;83:1749-51.
  • 76
    Nofal A, Fawzy MM, Deen SMS, El-Hawary EE. Herpes zoster ophthalmicus in COVID-19 patients. Int J Dermatol. 2020;59:1545-6.
  • 77
    Boix-Vilanova J, Gracia-Darder I, Saus C, Ramos D, Llull A, Santonja C, et al. Grover-like skin eruption: another cutaneous manifestation in a COVID-19 patient. Int J Dermatol. 2020;59:1290-2.
  • 78
    Taşlıdere B, Mehmetaj L, Özcan AB, Gülen B, Taşlıdere N. Melkersson-Rosenthal Syndrome Induced by COVID-19. Am J Emerg Med. 2021;41:262.
  • 79
    Sipfle N, Bridwell RE, Roper J. Erythema nodosum-like rash in a COVID-19 patient: A case report. Am J Emerg Med. 2021;40:227.
  • 80
    Behbahani S, Baltz JO, Droms R, Deng AC, Amano SU, Levin NA, et al. Sarcoid-like reaction in a patient recovering from coronavirus disease 19 pneumonia. JAAD Case Rep. 2020;6:915-7.
  • 81
    Brin C, Sohier P, L’honneur AS, Marot S, Matar S, Aractingi S, et al. An Isolated Peculiar Gianotti-Crosti Rash in the Course of a COVID-19 Episode. Acta Derm Venereol. 2020;100:00276.
  • 82
    Alpalhão M, Gaibino N, Filipe P. Seborrheic dermatitis in COVID19: a case report. Int J Dermatol. 2020;59:1543-4.
  • 83
    Diaz-Guimaraens B, Dominguez-Santas M, Suarez-Valle A, Fernandez-Nieto D, Jimenez-Cauhe J, Ballester A. Annular lichen planus associated with coronavirus SARS-CoV-2 disease (COVID-19). Int J Dermatol. 2021;60:246-7.
  • 84
    Montinari M, Atzori L, Valdevit S, Rongioletti F. Erythema annulare centrifugum with anosmia and ageusia in a SARS-CoV-2 exposed patient successfully treated with doxycycline. Int J Dermatol. 2021;60:384-6.
  • 85
    Monte-Serrano J, García-Gil MF, García-García M, Casas-Flecha I, Matovelle-Ochoa C, Ara-Martín M, et al. Granuloma annulare triggered by SARS-CoV-2 infection: Immunohistochemical staining. Dermatol Ther. 2021;34:14897.
  • 86
    FIvenson D. COVID-19: association with rapidly progressive forms of alopecia areata. Int J Dermatol. 2021;60:127.
  • 87
    Kaya G, Kaya A, Saurat JH. Clinical and Histopathological Features and Potential Pathological Mechanisms of Skin Lesions in COVID-19: Review of the Literature. Dermatopathology (Basel). 2020;7:3-16.
  • 88
    Wambier CG, Goren A. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is likely to be androgen mediated. J Am Acad Dermatol. 2020;83:308-9.
  • 89
    Goren A, Wambier CG, Herrera S, McCoy J, Vano-Galvᘠn S, Gioia F, et al. Anti-androgens may protect against severe COVID-19 outcomes: results from a prospective cohort study of 77 hospitalized men. J Eur Acad Dermatol Venereol. 2021;35:13-5.
  • 90
    McCoy J, Cadegiani FA, Wambier CG, Herrera S, Vano-Galvᘠn S, Mesinkovska NA, et al. 5-alpha-reductase inhibitors are associated with reduced frequency of COVID-19 symptoms in males with androgenetic alopecia. J Eur Acad Dermatol Venereol. 2021;35:243-6.

Publication Dates

  • Publication in this collection
    18 Feb 2022
  • Date of issue
    2022

History

  • Received
    05 Aug 2021
  • Accepted
    22 Aug 2021
  • Published
    10 Nov 2021
Sociedade Brasileira de Dermatologia Av. Rio Branco, 39 18. and., 20090-003 Rio de Janeiro RJ, Tel./Fax: +55 21 2253-6747 - Rio de Janeiro - RJ - Brazil
E-mail: revista@sbd.org.br