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Dermatologic and Ophthalmologic Treatment of Erythema Multiforme Major: A Case Report

Erythema multiforme major (EMM) is a rare type IV cytotoxic reaction targeting keratinocytes of the mucosal surfaces and the dermis. Dusky, targetoid lesions with central clearing are classically present, which may become blistered and rupture. The disease is usually self-limited and managed with su...

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Autores principales: Senger, Barbara, Memar, Shayan A, Ahmann, Alex, Houser, Jeremy J, Doughty-McDonald, Lauren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8795857/
https://www.ncbi.nlm.nih.gov/pubmed/35111489
http://dx.doi.org/10.7759/cureus.20854
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author Senger, Barbara
Memar, Shayan A
Ahmann, Alex
Houser, Jeremy J
Doughty-McDonald, Lauren
author_facet Senger, Barbara
Memar, Shayan A
Ahmann, Alex
Houser, Jeremy J
Doughty-McDonald, Lauren
author_sort Senger, Barbara
collection PubMed
description Erythema multiforme major (EMM) is a rare type IV cytotoxic reaction targeting keratinocytes of the mucosal surfaces and the dermis. Dusky, targetoid lesions with central clearing are classically present, which may become blistered and rupture. The disease is usually self-limited and managed with supportive care and treatment of the underlying condition. The most common triggering factors are adverse reactions to medications, herpes simplex virus (HSV), and Mycoplasma pneumoniae. Rapid recognition of EMM is essential to avoid long-term complications. This case presents a 39-year-old male with a unique history of recent non-steroidal anti-inflammatory drug (NSAID) use, past infection with HSV-1, and an acute Mycoplasma pneumoniae infection. The patient developed painful lesions on the skin, oral mucosa, ocular surfaces, and urethra. The painful lesions caused complications with feeding and voiding. Initially, the triggering event was unclear. Supportive care was started. NSAIDs were discontinued and similarly-structured drugs were avoided. Treatments targeting Mycoplasma pneumoniae and HSV-1 were initiated while lab results were pending. Once the results returned, the treatment regimen of corticosteroids for inflammation, acyclovir for HSV-1, and azithromycin for Mycoplasma pneumoniae was continued. Vaseline was applied to open lesions. The patient was also treated with mouthwash consisting of aluminum (Al) hydroxide/magnesium (Mg) hydroxide/simethicone (400 mg/400 mg/40 mg). Topical 2% lidocaine gel with applicator was used to assist with urinary discomfort during voiding. Fentanyl was used for pain control. The patient successfully recovered and was discharged to follow-up with ophthalmology. Long-term sequelae including trichiasis, symblepharon, and punctal stenosis were noted during follow-up appointments.
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spelling pubmed-87958572022-02-01 Dermatologic and Ophthalmologic Treatment of Erythema Multiforme Major: A Case Report Senger, Barbara Memar, Shayan A Ahmann, Alex Houser, Jeremy J Doughty-McDonald, Lauren Cureus Dermatology Erythema multiforme major (EMM) is a rare type IV cytotoxic reaction targeting keratinocytes of the mucosal surfaces and the dermis. Dusky, targetoid lesions with central clearing are classically present, which may become blistered and rupture. The disease is usually self-limited and managed with supportive care and treatment of the underlying condition. The most common triggering factors are adverse reactions to medications, herpes simplex virus (HSV), and Mycoplasma pneumoniae. Rapid recognition of EMM is essential to avoid long-term complications. This case presents a 39-year-old male with a unique history of recent non-steroidal anti-inflammatory drug (NSAID) use, past infection with HSV-1, and an acute Mycoplasma pneumoniae infection. The patient developed painful lesions on the skin, oral mucosa, ocular surfaces, and urethra. The painful lesions caused complications with feeding and voiding. Initially, the triggering event was unclear. Supportive care was started. NSAIDs were discontinued and similarly-structured drugs were avoided. Treatments targeting Mycoplasma pneumoniae and HSV-1 were initiated while lab results were pending. Once the results returned, the treatment regimen of corticosteroids for inflammation, acyclovir for HSV-1, and azithromycin for Mycoplasma pneumoniae was continued. Vaseline was applied to open lesions. The patient was also treated with mouthwash consisting of aluminum (Al) hydroxide/magnesium (Mg) hydroxide/simethicone (400 mg/400 mg/40 mg). Topical 2% lidocaine gel with applicator was used to assist with urinary discomfort during voiding. Fentanyl was used for pain control. The patient successfully recovered and was discharged to follow-up with ophthalmology. Long-term sequelae including trichiasis, symblepharon, and punctal stenosis were noted during follow-up appointments. Cureus 2021-12-31 /pmc/articles/PMC8795857/ /pubmed/35111489 http://dx.doi.org/10.7759/cureus.20854 Text en Copyright © 2021, Senger et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Dermatology
Senger, Barbara
Memar, Shayan A
Ahmann, Alex
Houser, Jeremy J
Doughty-McDonald, Lauren
Dermatologic and Ophthalmologic Treatment of Erythema Multiforme Major: A Case Report
title Dermatologic and Ophthalmologic Treatment of Erythema Multiforme Major: A Case Report
title_full Dermatologic and Ophthalmologic Treatment of Erythema Multiforme Major: A Case Report
title_fullStr Dermatologic and Ophthalmologic Treatment of Erythema Multiforme Major: A Case Report
title_full_unstemmed Dermatologic and Ophthalmologic Treatment of Erythema Multiforme Major: A Case Report
title_short Dermatologic and Ophthalmologic Treatment of Erythema Multiforme Major: A Case Report
title_sort dermatologic and ophthalmologic treatment of erythema multiforme major: a case report
topic Dermatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8795857/
https://www.ncbi.nlm.nih.gov/pubmed/35111489
http://dx.doi.org/10.7759/cureus.20854
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