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A rare case of pyoderma gangrenosum occurring at the site of laparoscopic port following laparoscopic radical nephrectomy
INTRODUCTION: Pyoderma gangrenosum is a rare dermatological disease associated with underlying inflammatory conditions. CASE PRESENTATION: A 59‐year‐old man was diagnosed with right renal cancer cT1aN0M0 and laparoscopic right radical nephrectomy was performed. Five days after surgery, he had a high...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436675/ https://www.ncbi.nlm.nih.gov/pubmed/36090933 http://dx.doi.org/10.1002/iju5.12505 |
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author | Ogasawara, Takuto Fukuta, Fumimasa Fujita, Miri Tachiki, Hitoshi Shindo, Tetsuya Kato, Junji Uhara, Hisashi Masumori, Naoya |
author_facet | Ogasawara, Takuto Fukuta, Fumimasa Fujita, Miri Tachiki, Hitoshi Shindo, Tetsuya Kato, Junji Uhara, Hisashi Masumori, Naoya |
author_sort | Ogasawara, Takuto |
collection | PubMed |
description | INTRODUCTION: Pyoderma gangrenosum is a rare dermatological disease associated with underlying inflammatory conditions. CASE PRESENTATION: A 59‐year‐old man was diagnosed with right renal cancer cT1aN0M0 and laparoscopic right radical nephrectomy was performed. Five days after surgery, he had a high‐grade fever, surgical site flare, and severe pain. At first, we diagnosed surgical site infection and wound dehiscence. Despite treatment for infection, his general condition and dermatological symptoms did not improve. Thereafter, a dermatologist advised us to perform a skin biopsy and blood culture examinations. Finally, the man was diagnosed with pyoderma gangrenosum according to the pathology of the skin biopsy and negative blood culture. After both intravenous administration of predonisolone and a topical corticosteroid, the high‐grade fever and dermatological symptoms improved greatly. CONCLUSION: Although pyoderma gangrenosum is a rare disease, we should bear in mind the disease since the treatment strategy is completely different from that for surgical site infection. |
format | Online Article Text |
id | pubmed-9436675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94366752022-09-09 A rare case of pyoderma gangrenosum occurring at the site of laparoscopic port following laparoscopic radical nephrectomy Ogasawara, Takuto Fukuta, Fumimasa Fujita, Miri Tachiki, Hitoshi Shindo, Tetsuya Kato, Junji Uhara, Hisashi Masumori, Naoya IJU Case Rep Case Reports INTRODUCTION: Pyoderma gangrenosum is a rare dermatological disease associated with underlying inflammatory conditions. CASE PRESENTATION: A 59‐year‐old man was diagnosed with right renal cancer cT1aN0M0 and laparoscopic right radical nephrectomy was performed. Five days after surgery, he had a high‐grade fever, surgical site flare, and severe pain. At first, we diagnosed surgical site infection and wound dehiscence. Despite treatment for infection, his general condition and dermatological symptoms did not improve. Thereafter, a dermatologist advised us to perform a skin biopsy and blood culture examinations. Finally, the man was diagnosed with pyoderma gangrenosum according to the pathology of the skin biopsy and negative blood culture. After both intravenous administration of predonisolone and a topical corticosteroid, the high‐grade fever and dermatological symptoms improved greatly. CONCLUSION: Although pyoderma gangrenosum is a rare disease, we should bear in mind the disease since the treatment strategy is completely different from that for surgical site infection. John Wiley and Sons Inc. 2022-07-15 /pmc/articles/PMC9436675/ /pubmed/36090933 http://dx.doi.org/10.1002/iju5.12505 Text en © 2022 The Authors. IJU Case Reports published by John Wiley & Sons Australia, Ltd on behalf of Japanese Urological Association. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Ogasawara, Takuto Fukuta, Fumimasa Fujita, Miri Tachiki, Hitoshi Shindo, Tetsuya Kato, Junji Uhara, Hisashi Masumori, Naoya A rare case of pyoderma gangrenosum occurring at the site of laparoscopic port following laparoscopic radical nephrectomy |
title | A rare case of pyoderma gangrenosum occurring at the site of laparoscopic port following laparoscopic radical nephrectomy |
title_full | A rare case of pyoderma gangrenosum occurring at the site of laparoscopic port following laparoscopic radical nephrectomy |
title_fullStr | A rare case of pyoderma gangrenosum occurring at the site of laparoscopic port following laparoscopic radical nephrectomy |
title_full_unstemmed | A rare case of pyoderma gangrenosum occurring at the site of laparoscopic port following laparoscopic radical nephrectomy |
title_short | A rare case of pyoderma gangrenosum occurring at the site of laparoscopic port following laparoscopic radical nephrectomy |
title_sort | rare case of pyoderma gangrenosum occurring at the site of laparoscopic port following laparoscopic radical nephrectomy |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436675/ https://www.ncbi.nlm.nih.gov/pubmed/36090933 http://dx.doi.org/10.1002/iju5.12505 |
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