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Anti-MDA-5 Dermatomyositis With Development of Drug-Mediated Necrolytic Skin Lesions

A 59-year-old male presented with 1 month of progressive dyspnea, 30-lb weight loss, and skin changes on the digits of the hands. In the 4 weeks prior to admission, he was admitted and treated twice for pneumonia at another hospital and received intravenous (IV) vancomycin, ceftriaxone, and azithrom...

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Autores principales: Case, Robert A., Patel, Vishal, Mejia-Otero, Carolina, Siroy, Alan E., Patel, Divya C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7350393/
https://www.ncbi.nlm.nih.gov/pubmed/32643953
http://dx.doi.org/10.1177/2324709620940496
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author Case, Robert A.
Patel, Vishal
Mejia-Otero, Carolina
Siroy, Alan E.
Patel, Divya C.
author_facet Case, Robert A.
Patel, Vishal
Mejia-Otero, Carolina
Siroy, Alan E.
Patel, Divya C.
author_sort Case, Robert A.
collection PubMed
description A 59-year-old male presented with 1 month of progressive dyspnea, 30-lb weight loss, and skin changes on the digits of the hands. In the 4 weeks prior to admission, he was admitted and treated twice for pneumonia at another hospital and received intravenous (IV) vancomycin, ceftriaxone, and azithromycin for a total of 10 days. After admission, he underwent computed tomography imaging of chest, which revealed findings suggestive of interstitial lung disease but given the fact that infection was not ruled out, empiric antibiotics were initiated. The skin lesions on the fingers were felt to be consistent with Gottron’s papules, and his overall constellation of findings were felt to be consistent with dermatomyositis (DM). Over the following 3 days, he developed diffuse, violaceous skin lesions, elevation of liver transaminases, and severe thrombocytopenia. The skin lesions progressed to epidermal necrosis. He developed erosions of the oral mucosa and scrotum. Before skin biopsy results were finalized, IV immunoglobulin and IV dexamethasone were started empirically for suspected DM and immune-mediated thrombocytopenia. His laboratory abnormalities normalized within a week. Biopsy results of the skin were consistent with Stevens-Johnson syndrome (SJS). Autoantibody test for anti-MDA5 were positive, confirming a diagnosis of anti-MDA5 associated DM. Subsequent development of SJS was likely due to antibiotic exposure in the preceding month. Simultaneous development of anti-MDA5 DM and SJS raises the question of a link between the 2 conditions. To our knowledge, this is the first reported association of these 2 conditions reported in the literature.
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spelling pubmed-73503932020-07-20 Anti-MDA-5 Dermatomyositis With Development of Drug-Mediated Necrolytic Skin Lesions Case, Robert A. Patel, Vishal Mejia-Otero, Carolina Siroy, Alan E. Patel, Divya C. J Investig Med High Impact Case Rep Case Report A 59-year-old male presented with 1 month of progressive dyspnea, 30-lb weight loss, and skin changes on the digits of the hands. In the 4 weeks prior to admission, he was admitted and treated twice for pneumonia at another hospital and received intravenous (IV) vancomycin, ceftriaxone, and azithromycin for a total of 10 days. After admission, he underwent computed tomography imaging of chest, which revealed findings suggestive of interstitial lung disease but given the fact that infection was not ruled out, empiric antibiotics were initiated. The skin lesions on the fingers were felt to be consistent with Gottron’s papules, and his overall constellation of findings were felt to be consistent with dermatomyositis (DM). Over the following 3 days, he developed diffuse, violaceous skin lesions, elevation of liver transaminases, and severe thrombocytopenia. The skin lesions progressed to epidermal necrosis. He developed erosions of the oral mucosa and scrotum. Before skin biopsy results were finalized, IV immunoglobulin and IV dexamethasone were started empirically for suspected DM and immune-mediated thrombocytopenia. His laboratory abnormalities normalized within a week. Biopsy results of the skin were consistent with Stevens-Johnson syndrome (SJS). Autoantibody test for anti-MDA5 were positive, confirming a diagnosis of anti-MDA5 associated DM. Subsequent development of SJS was likely due to antibiotic exposure in the preceding month. Simultaneous development of anti-MDA5 DM and SJS raises the question of a link between the 2 conditions. To our knowledge, this is the first reported association of these 2 conditions reported in the literature. SAGE Publications 2020-07-09 /pmc/articles/PMC7350393/ /pubmed/32643953 http://dx.doi.org/10.1177/2324709620940496 Text en © 2020 American Federation for Medical Research https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Case, Robert A.
Patel, Vishal
Mejia-Otero, Carolina
Siroy, Alan E.
Patel, Divya C.
Anti-MDA-5 Dermatomyositis With Development of Drug-Mediated Necrolytic Skin Lesions
title Anti-MDA-5 Dermatomyositis With Development of Drug-Mediated Necrolytic Skin Lesions
title_full Anti-MDA-5 Dermatomyositis With Development of Drug-Mediated Necrolytic Skin Lesions
title_fullStr Anti-MDA-5 Dermatomyositis With Development of Drug-Mediated Necrolytic Skin Lesions
title_full_unstemmed Anti-MDA-5 Dermatomyositis With Development of Drug-Mediated Necrolytic Skin Lesions
title_short Anti-MDA-5 Dermatomyositis With Development of Drug-Mediated Necrolytic Skin Lesions
title_sort anti-mda-5 dermatomyositis with development of drug-mediated necrolytic skin lesions
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7350393/
https://www.ncbi.nlm.nih.gov/pubmed/32643953
http://dx.doi.org/10.1177/2324709620940496
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