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Dorsal thermal necrosis in a Brazilian sheep flock

Necrose térmica dorsal em rebanho ovino brasileiro

ABSTRACT:

Thermal burn injuries are very uncommon occurrences in small ruminants worldwide, and in Brazil, there are no descriptions of this condition. Herein we describe an outbreak of dorsal thermal necrosis in a flock of sheep in the municipality of Boca da Mata, in the Forest Zone of the State of Alagoas, Northeastern Brazil. Twelve ewes were separated from the flock for a general clinical examination and evaluation the serum levels of urea, creatinine, gamma-glutamyltransferase, and aspartate aminotransferase. In addition, biopsies of the skin and liver were performed on two severely affected sheep. The flock was raised in semi-intensively management in a pasture area without shading and receiving approximately eight hours of insolation daily and developed severe dermatitis that evolved to severe necrosis of the dorsal skin. Grossly, these lesions were only observed in the dorsal skin of black sheep, while sheep with white dorsal areas of skin were not affected. Microscopically, the epidermis and deep dermis of affected sheep showed diffuse coagulative necrosis, pigmentary incontinence, and parakeratotic hyperkeratosis. Dorsal thermal necrosis occurs only in the dorsal skin of black sheep in situations of excessive exposure to sunlight due to the accumulation of ultraviolet radiation. The distribution of the lesions, restricted to the dorsal area of the skin, is an important clinicopathological aspect in these cases that can help differentiate lesions caused by photosensitization, as they usually involve other anatomical sites. To the authors’ knowledge, this is the first report of dorsal thermal necrosis in sheep in Brazil.

INDEX TERMS:
Thermal necrosis; sheep; solar radiation; small ruminants; skin; dry gangrene; Brazilian northeastern

RESUMO:

Lesões por queimaduras térmicas são ocorrências muito incomuns em pequenos ruminantes no mundo e no Brasil não há registros da ocorrência desta condição. Descreve-se um surto de necrose térmica dorsal em um rebanho de ovinos no município de Boca da Mata, Zona da Mata do Estado de Alagoas, Nordeste do Brasil. Doze ovelhas foram separadas do rebanho para realização de exame clínico geral e avaliação dos níveis séricos de uréia, creatinina,gama-glutamiltransferase e aspartato aminotransferase. Adicionalmente, biópsias de pele e fígado foram realizadas em duas ovelhas severamente afetadas. O rebanho era criado sob manejo semi-intensivo em uma área de pastagem sem sombreamento e recebiam aproximadamente oito horas de insolação diárias. Essas ovelhas desenvolveram dermatite severa que evoluiu para necrose da pele dorsal. Macroscopicamente, as lesões foram observadas apenas na pele dorsal de ovelhas negras, enquanto ovelhas com áreas dorsais brancas da pele não foram afetadas. Microscopicamente, a epiderme e a derme profunda das ovelhas afetadas apresentavam necrose coagulativa difusa, além de incontinência pigmentar e hiperqueratose paraqueratótica. A necrose térmica dorsal ocorre apenas na pele dorsal de ovelhas negras em situações de exposição excessiva à luz solar devido ao acúmulo de radiação ultravioleta. A distribuição das lesões, restrita à região dorsal da pele, é um importante aspecto clínico-patológico nesses casos que pode auxiliar na diferenciação das lesões causadas por fotossensibilização, pois geralmente envolvem outros sítios anatômicos. Este é o primeiro relato de necrose térmica dorsal em ovinos no Brasil.

TERMOS DE INDEXAÇÃO:
Necrose térmica; ovinos; radiação solar; pequenos ruminantes; pele; gangrena seca; nordeste brasileiro

Introduction

Solar radiation is composed of variable wavelengths of ultraviolet (UV) rays, mainly UVA (320-400nm) and UVB (290-320nm) rays (Ferramola de Sancovich & Sancovich 2006Ferramola de Sancovich A.M. & Sancovich H.A. 2006. Interacciones de las radiaciones electromagnéticas y especies reactivas del oxígeno sobre la piel. Revta Argent. Dermatol. 87:113-120., Gonzáles-Púmariega et al. 2009Gonzáles-Púmariega M., Tamayo M.V. & Sánchez-Lamar Á. 2009. La radiación ultravioleta. Su efecto dañino y consecuencias para la salud humana. Theoria, 18(2):69-80., Luigi et al. 2016Luigi P.G., Rightler A.L., Heronc B.M. & Gabbuttc C.D. 2016. Extending human perception of electromagnetic radiation to the UV region through biologically inspired photochromic fuzzy logic (BIPFUL) systems. Chem. Commun. 52(7):1474-1477. <https://dx.doi.org/10.1039/c5cc09290f> <PMid:26658700>
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). The radiant energy of the sun, especially from UVB rays, is responsible for varying degrees of skin lesions, including burns, elastosis, fibrosis, comedones, adnexal cysts and keratosis (Mauldin & Peters-Kennedy 2015Mauldin E.A. & Peters-kennedy J. 2015. Integumentary system, p.509-756. In: Maxie M.G. (Ed.), Jubb, Kennedy and Palmer’s Pathology of Domestic Animals. Vol.1. 6th ed. Elsevier, London., Hossy et al. 2018Hossy B.H., Leitão A.A.C., Torres R.B., Ramos-E-Silva M., Miguel N.C.O. & De Pádula M. 2018. Histological observation of hairless mice skin after exposure to simulated solar light: Comparison between the histological findings with different methodologies and 3R principle correlations. Burns 44(2):359-369. <https://dx.doi.org/10.1016/j.burns.2017.08.011> <PMid:29032978>
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, Rousselet et al. 2019Rousselet E., Stolen M., Durden W.N., Jablonski T., Stacy N.I. & Rotstein D.S. 2019. Bilateral polycystic kidneys and focal renal cystadenoma in a pygmy sperm whale (Kogia breviceps). J. Wildl. Dis. 55(1):258-261. <https://dx.doi.org/10.7589/2018-01-019> <PMid:30235083>
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). In addition, solar radiation is also responsible for photosensitization, an exacerbated form of sunburn caused by the photodynamic chemical activation in the skin that are frequent in cases of poisoning by plants (Albernaz et al. 2010Albernaz T.T., Silveira J.A.S., Silva N.S., Oliveira C.H.S., Belo Reis A.S., Oliveira C.M.C., Duarte M.D. & Barbosa J.D. 2010. Fotossensibilização em ovinos associada à ingestão de Brachiaria brizantha no estado do Pará. Pesq. Vet. Bras. 30(9):741-748. <https://dx.doi.org/10.1590/S0100-736X2010000900006>
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, Araújo et al. 2017Araújo V.O., Oliveira Neto T.S., Simões S.V.D., Silva T.K.F., Riet-Correa F. & Lucena R.B. 2017. Primary photosensitization and contact dermatitis caused by Malachra fasciata Jacq. N.V. (Malvaceae) in sheep. Toxicon 138:184-187. <https://dx.doi.org/10.1016/j.toxicon.2017.09.009> <PMid:28918228>
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, Mendonça & Riet-Correa 2023Mendonça F.S. & Riet-Correa F. 2023. Plantas que causam fotossensibilização primária, p.124-127. In: Riet-Correa F., Schild A.L., Lemos R., Borges J.R., Mendonça F.S. & Machado M. (Eds), Doenças de Ruminantes e Equídeos. Vol.2. 4ª ed. MedVet, São Paulo.). Despite producing lesions with some degree of similarity, solar dermatitis and photosensitivity are pathologically distinct.

The records of sun-induced dermatoses and tumors in humans have grown in recent decades, particularly in outdoor workers (Modenese et al. 2018Modenese A., Korpinen L. & Gobba F. 2018. Solar radiation exposure and outdoor work: an underestimated occupational risk. Int. J. Environ. Res. Publ. Health 15(10):2063. <https://dx.doi.org/10.3390/ijerph15102063> <PMid:30241306>
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, Gobba et al. 2019Gobba F., Modenese A. & John S.M. 2019. Skin cancer in outdoor workers exposed to solar radiation: a largely underreported occupational disease in Italy. J. Eur. Acad. Dermatol. 33(11):2068-2074. <https://dx.doi.org/10.1111/jdv.15768> <PMid:31265157>
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), which is directly related to the increase in radiation intensity (Kim & Kim 2018Kim H.-J. & Kim K.-H. 2018. Increased incidence of chronic actinic dermatitis in relation to climate changes and air pollution during the past 15 years in Korea. Photodermatol. Photoimmunol. Photomed. 34(6):387-392. <https://dx.doi.org/10.1111/phpp.12402> <PMid:29889316>
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, Parker 2021Parker E.R. 2021. The influence of climate change on skin cancer incidence - a review of the evidence. Int. J. Women’s Dermatol. 7(1):17-27. <https://dx.doi.org/10.1016/j.ijwd.2020.07.003> <PMid:33537393>
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) as well as the time of sun exposure. Despite the sporadic records in veterinary medicine, we believe that actinic diseases are underdiagnosed, particularly because the levels of sun exposure in the Brazilian Northeastern Region can be significantly high due to the proximity of this region to the equatorial line, and due to an increase in global temperature and thermal sensation, and reduction of the rainy days’ frequency (Narayanan et al. 2010Narayanan D.L., Saladi R.N. & Fox J.L. 2010. Ultraviolet radiation and skin cancer. Int. J. Dermatol. 49(9):978-986. <https://dx.doi.org/10.1111/j.1365-4632.2010.04474.x> <PMid:20883261>
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, Marengo et al. 2019Marengo J.A., Cunha A.P., Soares W.R., Torres R.R., Alves L.M., Brito S.S.B., Cuartas L.A., Leal K., Ribeiro Neto G., Alvalá R.C.S. & Magalhães A.R. 2019. Increase risk of drought in the semiarid lands of Northeast Brazil due to regional warming above 4°C, p.181-200. In: Nobre C.A., Marengo J.A. & Soares W.R. (Eds), Climate Change Risks in Brazil. Springer, Cham. <https://dx.doi.org/10.1007/978-3-319-92881-4_7>
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, Costa et al. 2020Costa R.L., Baptista G.M.M., Gomes H.B., Silva F.D.S., Rocha Júnior R.L., Salvador M.A. & Herdies D.L. 2020. Analysis of climate extremes indices over northeast Brazil from 1961 to 2014. Weather Clim. 28:100254. <https://dx.doi.org/10.1016/j.wace.2020.100254>
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).

Among actinic diseases, dorsal skin necrosis stands out. This condition was described in eight sheep in Uruguay. It was characterized by extensive, wide, and linear necrosis of the dorsal skin, extending from the interscapular to the lumbosacral area in eight sheep with black skin (García et al. 2019García J.A., Romero A., Uzal F.A., Tarigo L., Affolter V.K. & Dutra F. 2019. Solar-induced dorsal skin necrosis in sheep. Vet. Dermatol. 30(5):442-e137. <https://dx.doi.org/10.1111/vde.12777> <PMid:31342594>
https://doi.org/https://dx.doi.org/10.11...
). The lesion is compatible with a burn and occurs because black skin absorbs approximately 45% more solar radiation than white skin and can produce thermal energy, causing tissue carbonization (Mauldin & Peters-Kennedy 2015Mauldin E.A. & Peters-kennedy J. 2015. Integumentary system, p.509-756. In: Maxie M.G. (Ed.), Jubb, Kennedy and Palmer’s Pathology of Domestic Animals. Vol.1. 6th ed. Elsevier, London.). Despite its relevance and abundant predisposing factors in the Northeast of Brazil, there are no reports of dorsal skin necrosis in this region. The aim of this study was to report an outbreak of dorsal thermal necrosis diagnosed in a flock of sheep in the Forest Zone of the State of Alagoas, Northeastern Brazil.

Materials and Methods

Animal procedures were carried out in accordance with the National Institutes of Health Guide for the Care and Use of Animals and the “Conselho Nacional de Controle de Experimentação Animal”, “Ministério da Ciência e Tecnologia” (CONCEA/MCTI), Brazil.

An outbreak of dorsal thermal necrosis was observed in a flock of sheep in the municipality of Boca da Mata (S 9°38’31’’ and W 36°13’11’’), Forest Zone of the State of Alagoas, Northeastern Brazil, in the year 2022. The region has dissected relief and deep valleys, in addition to predominantly subperennial forest vegetation type, with parts of hypoxerophilic forest. The climate is tropical rainy, with a dry summer and a rainy period that begins in December/January and ends in September (Mascarenhas et al. 2005Mascarenhas J.C., Beltrão B.A., Souza Júnior L.C. 2005. Projeto Cadastro de Fontes de Abastecimento por Água Subterrânea. Serviço Geológico do Brasil, CPRM/PRODEEM, Recife, p.1-12. (Relatórios Técnicos).). During the disease investigation, 12 ewes, ~2-year-old showing deep and fetid skin wounds extending from the interscapular to the lumbosacral region, were evaluated. Clinical examination was performed according to Dirksen et al. (1993)Dirksen G., Gründer H.-D. & Stöber M. 1993. Rosenberg, Die Klinische Untersuchung des Rindes. 3rd ed. Verlagbuchhandlung Paul Parey, Berlin and Hamburg., and blood samples were collected using a vacuum collection system with silicone tubes with and without EDTA with a 5-mL capacity. The blood was centrifuged (110.682 G for 5 min), and serum was separated in polyethylene tubes, frozen at -20°C and stored for further analysis. Serum levels of urea and creatinine and serum activities of gamma-glutamyltransferase (GGT) and aspartate aminotransferase (AST) were evaluated using a colorimetric test using commercial kits in a semiautomatic biochemical analyzer LabQuest®.

Skin biopsies were collected aseptically using a 5mm skin punch from two severely affected sheep. In addition, a blind percutaneous liver biopsy was performed with a Menghini needle, according to Rocha et al. (2016)Rocha B.P., Reis M.O., Driemeier D., Cook D., Camargo L.M., Riet-Correa F., Evêncio-Neto J. & Mendonça F.S. 2016. Biópsia hepática como método diagnóstico para intoxicação por plantas que contêm swainsonina. Pesq. Vet. Bras. 36(5):373-377. <https://dx.doi.org/10.1590/S0100-736X2016000500003>
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. For this, a Menghini needle was introduced in the cranioventral direction, in the 11th right intercostal space, at the point of intersection with an imaginary line parallel to the spine, starting from the lateral end of the iliac tuberosity. After passing through the thoracic wall, the needle was introduced into the hepatic parenchyma for two to three centimeters to collect the samples. Samples were fixed in 10% buffered formalin (pH 7.2) for 24 hours. These samples were processed routinely to produce 4-μm thick sections stained with hematoxylin and eosin (HE). Additionally, the pasture was inspected to investigate toxic plants causing photosensitization.

Results

This outbreak was diagnosed in twelve ewes (29.26%) out of 41 crossbred sheep, with predominantly short brown, black and black/white coats. This flock was bought from another farm in the same region to be used as breeders in the new farm. At the original farm, the sheep were kept exclusively in a confinement system with access to shaded areas. After being transferred and placed for grazing from 8:00 a.m. until 4:00 p.m. (~8h/day) in a pasture of Panicum maximum without shading, two out of the foreign ewes presented skin lesions nine days after they were transferred to the pasture and after 17 days, 10 ewes presented the same lesions (10/26). These lesions were restricted to the dorsum and were limited to the black or brown areas of skin in dark-colored sheep; however, sheep with black skin and white coats or areas of black/white transition were also mildly affected (Fig.1).

Fig.1-4.
(1) Ewes showing varying degrees of skin necrosis. Note two severely affected ewes presenting lesions in the dorsal region and other individuals with smaller lesions, mostly in the dark skin or transitional areas. (2 and 3) Dry gangrene on dorsal skin, extending from the cervical to the sacral region. The edges of the necrotic skin were dry and firm. (4) Also note the diffusely reddened and raised overlying muscle, suggesting severe inflammation. The overlying muscle exhibited white to yellow (cervical region) and red to black (along the dorsum) devitalized areas associated with yellow fibrillar material.

Initially, the skin showed a linear to serpiginous ulceration along the dorsum (Fig.2), which evolved over a week to complete necrosis and detachment (Fig.3). In the first two sheep affected, these areas were extensive and deep, revealing the overlying longissimus dorsi and spinalis muscles (Fig.4). On average, the affected regions measured 48cm in length x 10cm in width. These animals had worse nutritional status (score 2) and arched their backs when handled. During the dermatological examination, the skin in the dorsal region continued to detach, exhaling a fetid odor combined with an adhered yellowish fibrillar material. The gangrenous skin was dry (mummified appearance) and dark gray to black. Nodular areas suggestive of granulation tissue, small fistulous tracts and epithelial retraction areas were additionally observed.

The other sheep were less affected and exhibited wounds gradually healing by secondary intention. Wool in white and black areas sheds easily, falling out in tufts. In short-haired animals, areas of white fur exhibited alopecia but no necrosis. No hematological alterations were observed in any sheep, and the serum levels of GGT, AST, serum creatinine and urea were within the reference values (Table 1).

Table 1.
Serum biochemistry findings from affected sheep with sun-induced dermal necrosis (n=2)

Microscopically, a focally extensive area of coagulative necrosis was observed affecting the epidermis and dermis was noted (Fig.5). Numerous bacterial myriads in the epidermis, deep dermis and muscle fibers were also observed. In segments with the epidermis intact, microabscesses were found in the stratum corneum (intracorneal) and in the epidermis (intraepidermal), in addition to spongiosis of keratinocytes, pigmentary incontinence and parakeratotic hyperkeratosis. Additionally, a focally extensive area of ulcer covered by a fibrinolytic membrane was noted. In the superficial dermis, there was a dense mixed inflammatory infiltrate, predominantly of neutrophils, followed by lymphocytes and macrophages. Extensive granulation tissue was noted in the deep dermis, accompanied by vasculitis and fibrin thrombi (Fig.6). No microscopic changes in the liver biopsy were noted in affected sheep (Fig.6 inset).

Fig.5-6.
(5) Marked coagulative necrosis effacing the epidermis and infiltrate occupying the deep dermis. Note the occurrence of only remnants of skin appendages. HE, obj.10x. (6) Granulation tissue in the dermis, involving a fibrin thrombus in the center. Normal liver parenchyma of affected sheep from which it can be concluded that the skin lesions are not related to hepatogenous photosensitization (inset). HE, obj.40x.

Discussion

This manuscript seems to report for the first time in Brazil an outbreak of thermal necrosis of dorsal skin in sheep. The epidemiological data, skin lesions restricted to the dorsal areas of the body, the significantly higher occurrence and severity in black and brown ewes, and the biochemical and gross and microscopic findings of the affected skin strongly suggest a thermal injury associated with prolonged sunlight exposure; as well as the sudden change in the management, exposure of ewes, used to being in the shade, to long sunlight exposure, plus the absence of shading triggered the skin lesions.

Dorsal thermal necrosis (DTN) is an uncommonly recognized thermal burn injury attributed to prolonged sun exposure and high environmental temperatures. In this condition, black skin/coat is remarkably severely affected, as the skin absorbs approximately 45% more solar radiation than white skin. In addition, the absorption of visible light (400-700nm) can produce thermal energy, causing burns with the carbonization of tissues (Fadare et al. 2012Fadare A.O., Peters S.O., Yakubu A., Sonibare A.O., Adeleke M.A., Ozoje M.O. & Imumorin I.G. 2012. Physiological and haematological indices suggest superior heat tolerance of white-coloured West African Dwarf sheep in the hot humid tropics. Trop. Anim. Health Prod. 45:157-165. <https://dx.doi.org/10.1007/s11250-012-0187-0> <PMid:22639037>
https://doi.org/https://dx.doi.org/10.10...
, Mauldin & Peters-Kennedy 2015Mauldin E.A. & Peters-kennedy J. 2015. Integumentary system, p.509-756. In: Maxie M.G. (Ed.), Jubb, Kennedy and Palmer’s Pathology of Domestic Animals. Vol.1. 6th ed. Elsevier, London., Leite et al. 2018Leite J.H.G.M., Silva R.G., Silva W.S.T., Silva W.E., Paiva R.D.M., Sousa J.E.R., Asensio L.A.B. & Façanha D.A.E. 2018. Locally adapted Brazilian ewes with different coat colors maintain homeothermy during the year in an equatorial semiarid environment. Int. J. Biometeorol. 62(9):1635-1644. <https://dx.doi.org/10.1007/s00484-018-1563-x> <PMid:30003337>
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). The energy from solar radiation can damage the skin via direct cell injury, increased thermal burden, or both (Werner 2016Werner A. 2016. Top 5 dermatoses associated with electromagnetic radiation. Clinician’s Brief. 93-97.).

Furthermore, it is important to highlight that the environment also affects the animal’s temperature throughout the day: animals exposed to the sun at warmer times, such as 1:00 p.m., show remaining levels of heat stored until 8:00 p.m. (Pulido-Rodríguez et al. 2021Pulido-Rodríguez L.F., Titto C.G., Bruni G.A., Froge G.A., Fuloni M.F., Payan-Carrera R., Henrique F.L., Geraldo A.C.A.P.M. & Pereira A.M.F. 2021. Effect of solar radiation on thermoregulatory responses of Santa Inês sheep and their crosses with wool and hair Dorper sheep. Small Rumin. Res. 202:106470. <https://dx.doi.org/10.1016/j.smallrumres.2021.106470>
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). These findings strengthen our theory, particularly when we consider the climatological indices of the Brazilian Northeast region. The geographic location of this region favors a more constant pattern of solar irradiance, high temperatures and longer photoperiods (Silva 2006Silva R.G. 2006. Predição da configuração de sombras de árvores em pastagens para bovinos. Eng. Agric. 26(1):268-281. <https://dx.doi.org/10.1590/S0100-69162006000100029>
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), whose values begin to increase from September onwards in the state of Alagoas (Amorim et al., 2019Amorim M.L.C.M., Saraiva E.P., Fonsêca V.F.C., Guerra R.R., Santos S.G.C.G., Costa C.C.M., Almeida M.E.V., Pinheiro A.C. & Pimenta Filho E.C. 2019. Coat and skin morphology of hair sheep breeds in an equatorial semi-arid environment. J. Therm. Biol. 84:103-110. <https://dx.doi.org/10.1016/j.jtherbio.2019.06.007>
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). In Uruguay, the lesion was described after sun exposure at 29°C, 8h/day, for ≥30 days. However, according to our results, average sun exposure at 30.7°C (MARKSIM®), 8h/day, for nine to fifteen days, was enough to cause severe skin lesions.

In animals experimentally exposed to the sun, more significant increases in body temperature were found in regions with a higher incidence of direct solar radiation, such as the back and shoulder (Pulido-Rodríguez et al. 2021Pulido-Rodríguez L.F., Titto C.G., Bruni G.A., Froge G.A., Fuloni M.F., Payan-Carrera R., Henrique F.L., Geraldo A.C.A.P.M. & Pereira A.M.F. 2021. Effect of solar radiation on thermoregulatory responses of Santa Inês sheep and their crosses with wool and hair Dorper sheep. Small Rumin. Res. 202:106470. <https://dx.doi.org/10.1016/j.smallrumres.2021.106470>
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), which may explain why this anatomical region is more severely affected because, in addition to direct exposure, it retains more energy absorbed during the day. Furthermore, in wooly breeds exposed to the sun of the Mediterranean climate, the wool surface reached 45°C. The skin temperature was 39.6°C, demonstrating that the effects of absorbed radiation remained mainly on the surface of the wool (Haddade et al. 2018Haddade I.R., Carreira E.R.S., Castro J.A.L., Carrilho S.R.F., Fragoso J., Geraldo A.C.A.P.M., Infante P. & Pereira A.M.F. 2018. Respostas fisiológicas comportamentais de ovelhas da raça Merino submetidas a elevadas temperaturas no ambiente do montado Alentejano. Revta Port. Zootec. (1):493-498.), which may explain why the wooly sheep exhibited fewer lesions when compared to the short-haired sheep. In reports of thermal necrosis in sheep, recent clipping was the main predisposing factor to injury in sheep (Butler & Bergman 2006Butler A.R. & Bergman E.L. 2006. Dermal necrosis of sheep following summer shearing. Proceedings of the Australian Society of Animal Production 26th Biennial Conference, Perth, West Australia, Australia. 46p., García et al. 2019García J.A., Romero A., Uzal F.A., Tarigo L., Affolter V.K. & Dutra F. 2019. Solar-induced dorsal skin necrosis in sheep. Vet. Dermatol. 30(5):442-e137. <https://dx.doi.org/10.1111/vde.12777> <PMid:31342594>
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).

The heat applied to the skin can cause necrotizing lesions of varying degrees. In this study, it is believed that the lesions correspond to 4th-degree burns. In these conditions, heat extends from the epidermis to the subcutaneous fascia, affecting blood and lymphatic vessels. This causes coagulative necrosis of connective tissues, blood vessels, and appendages; thrombosis and vascular leakage; dryness and charring of the epidermis, which flakes off and is filled with granulation tissue (Mauldin & Peters-Kennedy 2015Mauldin E.A. & Peters-kennedy J. 2015. Integumentary system, p.509-756. In: Maxie M.G. (Ed.), Jubb, Kennedy and Palmer’s Pathology of Domestic Animals. Vol.1. 6th ed. Elsevier, London.). These are the main mechanisms related to skin necrosis affecting mostly the dorsal areas of affected sheep in this study.

Previous reports of DTN in sheep are rare; it has only been described in Uruguay (García et al. 2019García J.A., Romero A., Uzal F.A., Tarigo L., Affolter V.K. & Dutra F. 2019. Solar-induced dorsal skin necrosis in sheep. Vet. Dermatol. 30(5):442-e137. <https://dx.doi.org/10.1111/vde.12777> <PMid:31342594>
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) and Australia (Butler & Bergman 2006Butler A.R. & Bergman E.L. 2006. Dermal necrosis of sheep following summer shearing. Proceedings of the Australian Society of Animal Production 26th Biennial Conference, Perth, West Australia, Australia. 46p.). This lack of knowledge, in our experience, has resulted in frequent misdiagnosis of DTN as other forms of dermatological disease, mostly primary or secondary photosensitization, that are ordinary diseases caused by several toxic plants in Brazil (Schwartz et al. 2018Schwartz S.L., Schick A.E., Lewis T.P. & Loeffler D. 2018. Dorsal thermal necrosis in dogs: a retrospective analysis of 16 cases in the southwestern USA (2009-2016). Vet. Derm. 29(2):139-e55. <https://dx.doi.org/10.1111/vde.12519> <PMid:29392813>
https://doi.org/https://dx.doi.org/10.11...
, Mendonça & Riet-Correa 2023Mendonça F.S. & Riet-Correa F. 2023. Plantas que causam fotossensibilização primária, p.124-127. In: Riet-Correa F., Schild A.L., Lemos R., Borges J.R., Mendonça F.S. & Machado M. (Eds), Doenças de Ruminantes e Equídeos. Vol.2. 4ª ed. MedVet, São Paulo.). DTN is also described in pigs (Frank et al. 2015Frank L.A., McCormick K.A., Donnell R.L. & Kania S.A. 2015. Dorsal black skin necrosis in a Vietnamese pot-bellied pig. Vet. Dermatol. 26(1):64-e23. <https://dx.doi.org/10.1111/vde.12181> <PMid:25354899>
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) and dogs (Schwartz et al. 2018Schwartz S.L., Schick A.E., Lewis T.P. & Loeffler D. 2018. Dorsal thermal necrosis in dogs: a retrospective analysis of 16 cases in the southwestern USA (2009-2016). Vet. Derm. 29(2):139-e55. <https://dx.doi.org/10.1111/vde.12519> <PMid:29392813>
https://doi.org/https://dx.doi.org/10.11...
). Other causes of thermal lesions in animals include hot liquids (Quist et al. 2012Quist E.M., Tanabe M., Mansell J.E.K.L. & Edwards J.L. 2012. A case series of thermal scald injuries in dogs exposed to hot water from garden hoses (garden hose scalding syndrome). Vet. Dermatol. 23(2):162-e33. <https://dx.doi.org/10.1111/j.1365-3164.2011.01015.x> <PMid:22132799>
https://doi.org/https://dx.doi.org/10.11...
), warming pads (Dunlop et al. 1989Dunlop C.I., Daunt D.A. & Haskins S.C. 1989. Thermal burns in four dogs during anesthesia. Vet. Surg. 18(3):242-246. <https://dx.doi.org/10.1111/j.1532-950x.1989.tb01079.x> <PMid:2773288>
https://doi.org/https://dx.doi.org/10.11...
), fire (Sharpe et al. 2020Sharpe A.N., Gunther-Harrington C.T., Epstein S.E., Li R.H.L. & Stern J.A. 2020. Cats with thermal burn injuries from California wildfires show echocardiographic evidence of myocardial thickening and intracardiac thrombi. Sci. Rep. 10:2648. <https://dx.doi.org/10.1038/s41598-020-59497-z>
https://doi.org/https://dx.doi.org/10.10...
, Rashid et al. 2021Rashid M., Naikoo M., Yadav C.L. & Taiswal K. 2021. Clinical management of second degree burns in Murrah buffaloes - A typical case report. Buffalo Bull. 40(3):503-507.), and electrical burns (Pereira et al. 2020Pereira A.A.B.G., Dias B., Castro S.I., Landi M.F.A., Melo C.B., Wilson T.M., Costa G.R.T., Passos P.H.O., Romano A.P., Szabo M.P.J. & Castro M.B. 2020. Electrocutions in free-living black-tufted marmosets (Callithrix penicillata) in anthropogenic environments in the Federal District and surrounding areas, Brazil. Primates 61(2):321-329. <https://dx.doi.org/10.1007/s10329-019-00760-x> <PMid:31564005>
https://doi.org/https://dx.doi.org/10.10...
). However, the skin lesions in these situations can occur in any part of the skin and are not limited to the dorsal skin, as reported here.

Differential dorsal thermal necrosis diagnoses include toxic epidermal necrolysis, erythema multiforme major, bullous pemphigoid, pemphigus vulgaris, vasculitis, and trauma. In Brazil, photosensitization (Albernaz et al. 2010Albernaz T.T., Silveira J.A.S., Silva N.S., Oliveira C.H.S., Belo Reis A.S., Oliveira C.M.C., Duarte M.D. & Barbosa J.D. 2010. Fotossensibilização em ovinos associada à ingestão de Brachiaria brizantha no estado do Pará. Pesq. Vet. Bras. 30(9):741-748. <https://dx.doi.org/10.1590/S0100-736X2010000900006>
https://doi.org/https://dx.doi.org/10.15...
, Araújo et al. 2017Araújo V.O., Oliveira Neto T.S., Simões S.V.D., Silva T.K.F., Riet-Correa F. & Lucena R.B. 2017. Primary photosensitization and contact dermatitis caused by Malachra fasciata Jacq. N.V. (Malvaceae) in sheep. Toxicon 138:184-187. <https://dx.doi.org/10.1016/j.toxicon.2017.09.009> <PMid:28918228>
https://doi.org/https://dx.doi.org/10.10...
) caused by Brachiaria spp., Froelichia humboldtiana and Malachra fasciata consumption should be considered. In these cases, the lesions are limited to white skin, mucous membranes, and vulvar and anal region areas. In fatal cases, heat stroke should be included (Bruchim et al. 2009Bruchim Y., Loeb E., Saragusty J. & Aroch I. 2009. Pathological findings in dogs with fatal heatstroke. J. Comp. Pathol. 140(2/3):97-104. <https://dx.doi.org/10.1016/j.jcpa.2008.07.011> <PMid:19111315>
https://doi.org/https://dx.doi.org/10.10...
). As for the pattern of skin injury, it should be considered that linear burns can occur on the back of animals exposed to hot water from hoses (Quist et al. 2012Quist E.M., Tanabe M., Mansell J.E.K.L. & Edwards J.L. 2012. A case series of thermal scald injuries in dogs exposed to hot water from garden hoses (garden hose scalding syndrome). Vet. Dermatol. 23(2):162-e33. <https://dx.doi.org/10.1111/j.1365-3164.2011.01015.x> <PMid:22132799>
https://doi.org/https://dx.doi.org/10.11...
) and injuries on the dorsolateral trunk are described in animals secondary to radiant heat and are characterized by irregular, alopecic, erythematous and hyperpigmented areas (Walder & Hargis 2002Walder E.J. & Hargis A.M. 2002. Chronic moderate heat dermatitis (erythema ab igne) in five dogs, three cats and one silvered langur. Vet. Dermatol. 13(5):283-292. <https://dx.doi.org/10.1046/j.1365-3164.2002.00304.x> <PMid:12358613>
https://doi.org/https://dx.doi.org/10.10...
).

Conclusions

Dorsal thermal necrosis (DTN) occurs due to multiple predisposing risk factors, including wool length, skin and wool pigmentation, prolonged sun exposure, high environmental temperature, and absence of shade.

The distribution of the lesions, restricted to the dorsal area of the skin, is an important clinicopathological aspect in these cases that can help differentiate lesions caused by photosensitization, as they usually involve other anatomical sites.

Acknowledgments

To the “Coordenação de Aperfeiçoamento de Pessoal de Nível Superior” (CAPES), Finance Code 001, and “Conselho Nacional de Desenvolvimento Científico e Tecnológico” (CNPq), Process 304804/2018-5 and Process 409116/2021-1), for granting the necessary financial support for the development of this study.

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Publication Dates

  • Publication in this collection
    20 Oct 2023
  • Date of issue
    2023

History

  • Received
    04 June 2023
  • Accepted
    04 July 2023
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