SciELO - Scientific Electronic Library Online

 
vol.86 issue4  suppl.1Autologous fat transplantation for the treatment of progressive hemifacial atrophy (Parry-Romberg syndrome: case report and review of medical literatute)Lúpus eritematoso sistêmico bolhoso: diagnóstico diferencial com dermatite herpetiforme author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Article

Indicators

Related links

  • Have no similar articlesSimilars in SciELO

Share


Anais Brasileiros de Dermatologia

Print version ISSN 0365-0596

An. Bras. Dermatol. vol.86 no.4 supl.1 Rio de Janeiro July/Aug. 2011

http://dx.doi.org/10.1590/S0365-05962011000700023 

CASE REPORT

 

Comedonic lupus: a rare presentation of discoid lupus erythematosus*

 

 

Daniela Ferro FariasI; Roberta Marinho Falcão GondimII; Isabella Portela RedighieriI; Helena MullerIII; Valéria PetriIV

ITrainee Physician of the Dermatology Service of the Hospital Ipiranga (HI) - Ipiranga (SP), Brasil
IIPhD Candidate - Faculdade de Medicina da Universidade de São Paulo (FMUSP) - São Paulo (SP), Brasil
IIIAssistant Teacher of the Pathology Department of the Faculdade de Ciências Médicas da Santa Casa de São Paulo (FCMSC-SP) - São Paulo (SP), Brasil
IVProfessor of the Departament of Dermatology of the Universidade Federal de São Paulo (UNIFESP) - São Paulo (SP), Brasil

Mailing address

 

 


ABSTRACT

Chronic cutaneous lupus erythematosus is a polymorphous autoimmune disease which may mimic some other clinical conditions, causing diagnostic difficulties. Acneiform lesions, including comedones and pitting scars are occasionally atypical presentations of cutaneous discoid lupus erythematosus.

Keywords: Lúpus erythematosus, cutaneous; Lúpus erythematosus, discoid; Lupus vulgaris


 

 

INTRODUCTION

Chronic cutaneous discoid lupus erythematosus (CCDLE) or discoid lupus eryhthematosus (DLE) is a rare chronic auto-immune dermatosis and the most common clinical variant of the lupus erythematosus (LE). It is caused or triggered by exposure to ultraviolet radiation, cold and drugs and develops gradually. The diagnosis of DLE is confirmed by histopathological examination. Uncommon clinical manifestations, like comedonic lupus can mimic other diseases like acne vulgaris, Favre-Racouchot disease, milium, milia en plaque, syringoma, tricoepithelioma, clustered dilated pores and nevus comedogenic.

 

CASE REPORT

35 years old female, reported a pruriginous acneiform eruption on the face for two years, which did not respond to conventional treatments for acne. The dermatologic examination showed lightly-colored violaceous, infiltrated plaques of various sizes and atrophic scars on the right ear, dorsal aspect of the nose and chin. Comedones and pitting scars were noted on a partially infiltrated plaque on the chin (Figure 1). CCLE was considered. The histopathological examination showed acanthosis, vacuolar degeneration of the basal cell layer, pigmentary incontinence, periadnexial mononuclear infiltrate, follicular plugging and comedones. PAS staining evidenced thickening of the basal membrane (BM) of the epidermis, more intense around the hair follicles (Figure 2).

 

 

 

 

Treatment started with sunscreen applied to the skin and systemic use of 500mg of tetracycline twice a day for three weeks and then 250mg twice a day for another thirty days. There was improvement of the pruritus and the number of comedones (Figure 3). With discontinuation of the tetracycline there was an acute recurrence of the lesions. The patient was then started on hydroxycloroquine 400mg daily with clinical improvement in 45 days (Figure 4). After six months of use of hydroxycloroquine there was marked improvement (Figure 5). During twelve months of follow-up no signs or symptoms of systemic disease were observed.

 

 

 

 

 

 

DISCUSSION

The clinical manifestations of CCLE are multiple and varied. The acneiform presentation of discoid CCLE is rare and only six cases have been reported so far. 1-7 this presentation is usually under diagnosed due to its similarity to inflammatory acne vulgaris. 1 The cases reported showed a predominance of women aged 25 to 35 and the symptoms that most commonly lead to the diagnosis were pruritus and photosensitivity. The cause of the comedogenic form of the CLE is not yet clear and the prognosis is uncertain. It is supposed that at least half of the patients with this condition have the tendency to develop systemic LE. 5

The differential diagnosis of comedogenic discoid CLE are: acne vulgaris, Favre-Racouchot disease, milium, milia em plaque, syringoma, tricoepithelioma, clustered dilated pores and nevus comedogenic. 5, 8 Acne vulgaris usually manifests as comedones and inflammatory papules and nodules, most commonly on the face and trunk. Favre-Racouchot disease, also known as 'cutaneous nodular elastoidosis with cysts and comedones' is characterized by volumous open, black comedones, located on the sun damaged skin of the elderly. 8 The nevus comedogenic, uncommon variant of the adnexial hamartoma, appears as linear groups of open comedones and, in 50% of the cases, they are present at birth. 5 Colloid milium is a rare degenerative disease, with development of small translucent, yellow to brown papules, nodules or plaques usually on sun damaged areas. 9 Milia en plaque is a rare clinical variant of the milium, characterized by multiple milium-like lesions over ery-thematous, edematous plaque, usually in middle-aged women. 10 Syringomas are adnexial tumors, more common in women, typically seen as soft, translucent or lightly yellow papules around the eyes. 10 Tricoepithelioma is a rare benign lesion, originated from the hair follicles, developing mostly on the face and scalp. 11

The diagnosis of comedonic DLE was confirmed mainly by the histopathological changes. The histological findings are comparable to those on the literature review, like: hydropic degeneration of the basal layer, thickening of the BM, follicular dilation, hyperkeratosis, lymphocyte inflammatory infiltrate, and melanophages on the dermis. 12 From all those, the most relevant findings to the establishment of the diagnosis of LE are the hydropic degeneration of the basal layer and the thickening of the BM, that occurs due to the deposition of reactive immune complexes and, in many cases, is seen only with the progression of the disease. 13 On the present case the identification of the comedones on the anatomopathological examination associated to the related changes permitted the confirmation of the diagnosis of comedonic LE.

Tetracycline was suggested at the beginning of the treatment and an antinflammatory and immunoregulator agent that has been successful on the treatment of acneiform conditions. 14 Other therapeutic options include oral hydroxycloroquine (400mg daily), topical tretinoin (0.025% cream), oral isotretinoin (1mg/kg/day), triamcinolone acetate (injected, 10mg/cc every 6 weeks), topical clobetasol (0.05% lotion twice a day) and mechanical extraction of the comedones. 1,3

The present case reinforces the importance of taking into consideration the various forms of presentation and the atypical behavior of discoid CLE, like the presence of acneiform lesions, accompanied by suggestive signs of CLE, that do not respond to conventional treatment to acne vulgaris.

 

REFERENCES

1. Stavrakoglou A, Hughes J, Coutts I. A case of discoid lupus erythematosus masquerading as acne. Acta Derm Venereol. 2008;88:175-6.         [ Links ]

2. Al-Refu K, Goodfield M. Scar classification in cutaneous lupus erythematosus: morphological description. Br J Dermatol. 2009;161:1052-8.         [ Links ]

3. Hemmati I, Otberg N, Martinka M, Alzoibani A, Restrepo I, Shapiro J. Discoid lupus erythematosus presenting with cysts, comedones, and cicatricial alopecia on the scalp. J Am Acad Dermatol 2009;60:1070-2.         [ Links ]

4. El Sayed F, Dhaybi R, Ammoury A, Bazex J. Lupus comédonien. Ann Dermatol Venereol. 2007;134:897-8.         [ Links ]

5. Chang YH, Wang SH, Chi CC. Discoid lupus erythematosus presenting as acneiform pitting scars. Int J Dermatol. 2006;45:944-5.         [ Links ]

6. Deruelle-Khazaal R, Ségard M, Cottencin-Charrière AC, Carotte-Lefebvre I, Thomas P. Chronic lupus erythematosus presenting as acneiform lesions. Ann Dermatol Venereol. 2002;129:883-5.         [ Links ]

7. Motel PJ, Bernstein EF, Fazio M, Hurrieniuk H, Kauh YC. Systemic lupus erythemato sus in patients diagnosed with treatment-resistant acne. Int J Dermatol 1995;34:338-40.         [ Links ]

8. Patterson WM, Fox MD, Schwartz RA. Favre-Racouchot disease. Int Soc Dermatol 2004;43:167-9.         [ Links ]

9. Rahman SB, Arfan Ul Bari, Mumtaz N. Colloid millium: a rare cutaneous deposition disease. J Pak Med Assoc. 2008;58:207-9.         [ Links ]

10. Cota C, Sinagra J, Donati P, Amantea A. Milia en plaque: three new pediatric cases. Pediatr Dermatol. 2009;26:717-20.         [ Links ]

11. Heller J, Roche N, Hameed M. Trichoepithelioma of the vulva: report of a case and review of the literature. J Low Genit Tract Dis. 2009;13:186-7.         [ Links ]

12. Berbert ALCV, Mantese SAO. Lúpus eritematoso cutâneo - aspectos clínicos e laboratoriais. An Bras Dermatol. 2005;80:119-31.         [ Links ]

13. Elder D, Elenistas R, Johson B Jr, Ioffreda M, Miller JJ, Miller OF. Histopatologia da pele de Lever. São Paulo: Editora Manole; 2001. p.129-30.         [ Links ]

14. Sapadin AN, Fleischmajer R. Tetracyclines: nonantibiotic properties and their clinical implications. J Am Acad Dermatol. 2006;54:258-65.         [ Links ]

 

 

Mailing address:
Daniela Ferro Farias
Ruas Leais Paulistanos - 400/6 apto 1083 Bairro: Ipiranga
042010 010 São Paulo SP, Brazil
E-mail: daniferro33@gmail.com

Received on 26.07.2010.
Approved by the Advisory Board and accepted for publication on 26.10.2010.
Conflict of interest: None
Financial funding: None

 

 

* Work performed at Hospital Ipiranga (HI) - São Paulo (SP), Brasil.