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Extensive Pyoderma Gangrenosum: A Challenging Diagnosis and Literature Review of Management

Pyoderma gangrenosum is a very rare, non-infectious leukocytic dermatosis, which is often associated with an underlying systemic disease. It is usually diagnosed based on the apparent clinical findings and by excluding other causes of ulcerative skin diseases. Treatment modality includes the use of...

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Autores principales: Yasin, Faizan, Assad, Salman, Zahid, Mehr, Malik, Shuja A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602483/
https://www.ncbi.nlm.nih.gov/pubmed/28944125
http://dx.doi.org/10.7759/cureus.1486
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author Yasin, Faizan
Assad, Salman
Zahid, Mehr
Malik, Shuja A
author_facet Yasin, Faizan
Assad, Salman
Zahid, Mehr
Malik, Shuja A
author_sort Yasin, Faizan
collection PubMed
description Pyoderma gangrenosum is a very rare, non-infectious leukocytic dermatosis, which is often associated with an underlying systemic disease. It is usually diagnosed based on the apparent clinical findings and by excluding other causes of ulcerative skin diseases. Treatment modality includes the use of systemic steroids and oral steroids. Immunosuppressive agents, such as cyclosporine and mycophenolate mofetil, can also be added if it fails to respond to steroids. We report a case of pyoderma gangrenosum in an 85-year-old female who presented in the inpatient facility with rapidly enlarging necrotic, ulcerative lesions with accompanying fever. She was managed with systemic steroids to which she responded well. This led to the arrest of the initially progressive lesions with some residual scarring.
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spelling pubmed-56024832017-09-22 Extensive Pyoderma Gangrenosum: A Challenging Diagnosis and Literature Review of Management Yasin, Faizan Assad, Salman Zahid, Mehr Malik, Shuja A Cureus Gastroenterology Pyoderma gangrenosum is a very rare, non-infectious leukocytic dermatosis, which is often associated with an underlying systemic disease. It is usually diagnosed based on the apparent clinical findings and by excluding other causes of ulcerative skin diseases. Treatment modality includes the use of systemic steroids and oral steroids. Immunosuppressive agents, such as cyclosporine and mycophenolate mofetil, can also be added if it fails to respond to steroids. We report a case of pyoderma gangrenosum in an 85-year-old female who presented in the inpatient facility with rapidly enlarging necrotic, ulcerative lesions with accompanying fever. She was managed with systemic steroids to which she responded well. This led to the arrest of the initially progressive lesions with some residual scarring. Cureus 2017-07-18 /pmc/articles/PMC5602483/ /pubmed/28944125 http://dx.doi.org/10.7759/cureus.1486 Text en Copyright © 2017, Yasin et al. http://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 Gastroenterology
Yasin, Faizan
Assad, Salman
Zahid, Mehr
Malik, Shuja A
Extensive Pyoderma Gangrenosum: A Challenging Diagnosis and Literature Review of Management
title Extensive Pyoderma Gangrenosum: A Challenging Diagnosis and Literature Review of Management
title_full Extensive Pyoderma Gangrenosum: A Challenging Diagnosis and Literature Review of Management
title_fullStr Extensive Pyoderma Gangrenosum: A Challenging Diagnosis and Literature Review of Management
title_full_unstemmed Extensive Pyoderma Gangrenosum: A Challenging Diagnosis and Literature Review of Management
title_short Extensive Pyoderma Gangrenosum: A Challenging Diagnosis and Literature Review of Management
title_sort extensive pyoderma gangrenosum: a challenging diagnosis and literature review of management
topic Gastroenterology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602483/
https://www.ncbi.nlm.nih.gov/pubmed/28944125
http://dx.doi.org/10.7759/cureus.1486
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