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An extensive pyoderma gangrenosum mimicking necrotizing fasciitis: An unusual case report
INTRODUCTION: Pyoderma Gangrenosum (PG) is a rare, benign and inflammatory disease characterized by ulcerative skin lesions. We report the successful management of an unusual case of PG following a caesarean section, with extensive cutaneous skin involvement and mimicking necrotizing fasciitis. PRES...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944046/ https://www.ncbi.nlm.nih.gov/pubmed/33691271 http://dx.doi.org/10.1016/j.ijscr.2021.105697 |
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author | Aziret, Mehmet Kara, Şeyma Yaldız, Mahizer Köse, Nur Aşıkuzunoğlu, Feyza Cevrioğlu, Arif Serhan |
author_facet | Aziret, Mehmet Kara, Şeyma Yaldız, Mahizer Köse, Nur Aşıkuzunoğlu, Feyza Cevrioğlu, Arif Serhan |
author_sort | Aziret, Mehmet |
collection | PubMed |
description | INTRODUCTION: Pyoderma Gangrenosum (PG) is a rare, benign and inflammatory disease characterized by ulcerative skin lesions. We report the successful management of an unusual case of PG following a caesarean section, with extensive cutaneous skin involvement and mimicking necrotizing fasciitis. PRESENTATION OF CASE: A 36-year-old woman was admitted with extensive surgical site inflammation after a caesarean section. Despite antibiotic treatment and wound care, the clinical course deteriorated rapidly. Wound debridement following negative pressure closure was performed due to an immediate increase in skin necrosis. A diagnosis of PG was reached based on the absence of a positive wound culture, resistance to wound debridement and the histopathological results. A course of high-dose corticosteroids was started, and a successful clinical course was finally achieved. The patient is now in the 14th month of remission, with no recurrence. DISCUSSION: PG is often reported after bowel surgery, especially after complicated stoma or diverticulitis, breast surgery and occasionally after C-sections. The diagnosis of pyoderma gangrenosum may be challenging because of a wide variety of macroscopic features and its pronounced similarity to necrotizing fasciitis. Treatment with systemic corticosteroids is the most common management option, while surgical treatment is extremely controversial. CONCLUSION: An extensive PG following surgery can mimic necrotizing fasciitis. An interdisciplinary treatment approach provides early diagnosis and effective treatment resulting in less morbidity. |
format | Online Article Text |
id | pubmed-7944046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-79440462021-03-16 An extensive pyoderma gangrenosum mimicking necrotizing fasciitis: An unusual case report Aziret, Mehmet Kara, Şeyma Yaldız, Mahizer Köse, Nur Aşıkuzunoğlu, Feyza Cevrioğlu, Arif Serhan Int J Surg Case Rep Case Report INTRODUCTION: Pyoderma Gangrenosum (PG) is a rare, benign and inflammatory disease characterized by ulcerative skin lesions. We report the successful management of an unusual case of PG following a caesarean section, with extensive cutaneous skin involvement and mimicking necrotizing fasciitis. PRESENTATION OF CASE: A 36-year-old woman was admitted with extensive surgical site inflammation after a caesarean section. Despite antibiotic treatment and wound care, the clinical course deteriorated rapidly. Wound debridement following negative pressure closure was performed due to an immediate increase in skin necrosis. A diagnosis of PG was reached based on the absence of a positive wound culture, resistance to wound debridement and the histopathological results. A course of high-dose corticosteroids was started, and a successful clinical course was finally achieved. The patient is now in the 14th month of remission, with no recurrence. DISCUSSION: PG is often reported after bowel surgery, especially after complicated stoma or diverticulitis, breast surgery and occasionally after C-sections. The diagnosis of pyoderma gangrenosum may be challenging because of a wide variety of macroscopic features and its pronounced similarity to necrotizing fasciitis. Treatment with systemic corticosteroids is the most common management option, while surgical treatment is extremely controversial. CONCLUSION: An extensive PG following surgery can mimic necrotizing fasciitis. An interdisciplinary treatment approach provides early diagnosis and effective treatment resulting in less morbidity. Elsevier 2021-02-26 /pmc/articles/PMC7944046/ /pubmed/33691271 http://dx.doi.org/10.1016/j.ijscr.2021.105697 Text en © 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Aziret, Mehmet Kara, Şeyma Yaldız, Mahizer Köse, Nur Aşıkuzunoğlu, Feyza Cevrioğlu, Arif Serhan An extensive pyoderma gangrenosum mimicking necrotizing fasciitis: An unusual case report |
title | An extensive pyoderma gangrenosum mimicking necrotizing fasciitis: An unusual case report |
title_full | An extensive pyoderma gangrenosum mimicking necrotizing fasciitis: An unusual case report |
title_fullStr | An extensive pyoderma gangrenosum mimicking necrotizing fasciitis: An unusual case report |
title_full_unstemmed | An extensive pyoderma gangrenosum mimicking necrotizing fasciitis: An unusual case report |
title_short | An extensive pyoderma gangrenosum mimicking necrotizing fasciitis: An unusual case report |
title_sort | extensive pyoderma gangrenosum mimicking necrotizing fasciitis: an unusual case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944046/ https://www.ncbi.nlm.nih.gov/pubmed/33691271 http://dx.doi.org/10.1016/j.ijscr.2021.105697 |
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