Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ogasawara, Takuto, Fukuta, Fumimasa, Fujita, Miri, Tachiki, Hitoshi, Shindo, Tetsuya, Kato, Junji, Uhara, Hisashi, Masumori, Naoya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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
_version_ 1784781422966341632
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
work_keys_str_mv AT ogasawaratakuto ararecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT fukutafumimasa ararecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT fujitamiri ararecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT tachikihitoshi ararecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT shindotetsuya ararecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT katojunji ararecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT uharahisashi ararecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT masumorinaoya ararecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT ogasawaratakuto rarecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT fukutafumimasa rarecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT fujitamiri rarecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT tachikihitoshi rarecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT shindotetsuya rarecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT katojunji rarecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT uharahisashi rarecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy
AT masumorinaoya rarecaseofpyodermagangrenosumoccurringatthesiteoflaparoscopicportfollowinglaparoscopicradicalnephrectomy