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Peritoneal Dialysis Exit Site Pyoderma Gangrenosum: A Case Report

BACKGROUND: Pyoderma gangrenosum (PG) is a rare, chronic inflammatory condition exhibiting mucopurulent or hemorrhagic exudates. The majority of cases are associated with inflammatory bowel disease, rheumatological diseases, and hematological malignancies. In the absence of typical serological marke...

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Autores principales: Anwar, Salman, Holfeld, Karen, Prasad, Bhanu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276769/
https://www.ncbi.nlm.nih.gov/pubmed/30574505
http://dx.doi.org/10.1159/000493188
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author Anwar, Salman
Holfeld, Karen
Prasad, Bhanu
author_facet Anwar, Salman
Holfeld, Karen
Prasad, Bhanu
author_sort Anwar, Salman
collection PubMed
description BACKGROUND: Pyoderma gangrenosum (PG) is a rare, chronic inflammatory condition exhibiting mucopurulent or hemorrhagic exudates. The majority of cases are associated with inflammatory bowel disease, rheumatological diseases, and hematological malignancies. In the absence of typical serological markers and specific histopathological changes, the diagnosis is often clinical. Being rare, it is frequently misdiagnosed, which leads to a delay in instituting appropriate therapy. CASE PRESENTATION: We present a 53-year-old male of Aboriginal descent with end-stage renal disease due to diabetes who underwent insertion of a peritoneal dialysis (PD) catheter. Five weeks after PD catheter insertion, he started to notice a painful ulcer surrounded by a bed of erythema. The lesion eventually progressed to a purulent, hemorrhagic ulcer surrounded by a raised, irregular, violaceous border along the entirety of the PD catheter tunnel. There was no history of underlying systemic diseases commonly associated with PG. The catheter was removed, and an elliptical biopsy was taken, which ruled out infection, malignancy, and vasculitis. The changes were felt to be consistent with PG. The patient underwent treatment initially with topical corticosteroids, followed by oral prednisone, which unfortunately worsened his diabetic control; due to this, he was transitioned to cyclosporine, with complete resolution. CONCLUSIONS: Lesions at the PD catheter exit site are usually treated for infections. However, for ulcers that are painful, rapidly expanding, nonhealing, and unresponsive to antibiotics, PG should be considered as a differential diagnosis. This is the first reported case of PG occurring at the exit site of a PD catheter.
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spelling pubmed-62767692018-12-20 Peritoneal Dialysis Exit Site Pyoderma Gangrenosum: A Case Report Anwar, Salman Holfeld, Karen Prasad, Bhanu Case Rep Nephrol Dial Case Report BACKGROUND: Pyoderma gangrenosum (PG) is a rare, chronic inflammatory condition exhibiting mucopurulent or hemorrhagic exudates. The majority of cases are associated with inflammatory bowel disease, rheumatological diseases, and hematological malignancies. In the absence of typical serological markers and specific histopathological changes, the diagnosis is often clinical. Being rare, it is frequently misdiagnosed, which leads to a delay in instituting appropriate therapy. CASE PRESENTATION: We present a 53-year-old male of Aboriginal descent with end-stage renal disease due to diabetes who underwent insertion of a peritoneal dialysis (PD) catheter. Five weeks after PD catheter insertion, he started to notice a painful ulcer surrounded by a bed of erythema. The lesion eventually progressed to a purulent, hemorrhagic ulcer surrounded by a raised, irregular, violaceous border along the entirety of the PD catheter tunnel. There was no history of underlying systemic diseases commonly associated with PG. The catheter was removed, and an elliptical biopsy was taken, which ruled out infection, malignancy, and vasculitis. The changes were felt to be consistent with PG. The patient underwent treatment initially with topical corticosteroids, followed by oral prednisone, which unfortunately worsened his diabetic control; due to this, he was transitioned to cyclosporine, with complete resolution. CONCLUSIONS: Lesions at the PD catheter exit site are usually treated for infections. However, for ulcers that are painful, rapidly expanding, nonhealing, and unresponsive to antibiotics, PG should be considered as a differential diagnosis. This is the first reported case of PG occurring at the exit site of a PD catheter. S. Karger AG 2018-11-14 /pmc/articles/PMC6276769/ /pubmed/30574505 http://dx.doi.org/10.1159/000493188 Text en Copyright © 2018 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Anwar, Salman
Holfeld, Karen
Prasad, Bhanu
Peritoneal Dialysis Exit Site Pyoderma Gangrenosum: A Case Report
title Peritoneal Dialysis Exit Site Pyoderma Gangrenosum: A Case Report
title_full Peritoneal Dialysis Exit Site Pyoderma Gangrenosum: A Case Report
title_fullStr Peritoneal Dialysis Exit Site Pyoderma Gangrenosum: A Case Report
title_full_unstemmed Peritoneal Dialysis Exit Site Pyoderma Gangrenosum: A Case Report
title_short Peritoneal Dialysis Exit Site Pyoderma Gangrenosum: A Case Report
title_sort peritoneal dialysis exit site pyoderma gangrenosum: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276769/
https://www.ncbi.nlm.nih.gov/pubmed/30574505
http://dx.doi.org/10.1159/000493188
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