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Pyoderma gangrenosum in a renal transplant recipient: A case report and review of literature
Pyoderma gangrenosum (PG) is a rare disorder of unknown etiology characterized by multiple cutaneous ulcers with mucopurulent or hemorrhagic exudate. This sterile neutrophilic dermatosis is known to occur in association with malignancy, infection, autoimmune disorders and drugs. Occurrence of PG in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588326/ https://www.ncbi.nlm.nih.gov/pubmed/26628796 http://dx.doi.org/10.4103/0971-4065.156900 |
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author | Jha, P. K. Rana, A. Kapoor, S. Kher, V. |
author_facet | Jha, P. K. Rana, A. Kapoor, S. Kher, V. |
author_sort | Jha, P. K. |
collection | PubMed |
description | Pyoderma gangrenosum (PG) is a rare disorder of unknown etiology characterized by multiple cutaneous ulcers with mucopurulent or hemorrhagic exudate. This sterile neutrophilic dermatosis is known to occur in association with malignancy, infection, autoimmune disorders and drugs. Occurrence of PG in a renal transplant recipient, who is already on immunosuppressants, is rare. We hereby report a renal transplant recipient who developed PG 1-month after transplant and responded well to treatment with escalated dose of oral steroid. |
format | Online Article Text |
id | pubmed-4588326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45883262015-12-01 Pyoderma gangrenosum in a renal transplant recipient: A case report and review of literature Jha, P. K. Rana, A. Kapoor, S. Kher, V. Indian J Nephrol Case Report Pyoderma gangrenosum (PG) is a rare disorder of unknown etiology characterized by multiple cutaneous ulcers with mucopurulent or hemorrhagic exudate. This sterile neutrophilic dermatosis is known to occur in association with malignancy, infection, autoimmune disorders and drugs. Occurrence of PG in a renal transplant recipient, who is already on immunosuppressants, is rare. We hereby report a renal transplant recipient who developed PG 1-month after transplant and responded well to treatment with escalated dose of oral steroid. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4588326/ /pubmed/26628796 http://dx.doi.org/10.4103/0971-4065.156900 Text en Copyright: © Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Jha, P. K. Rana, A. Kapoor, S. Kher, V. Pyoderma gangrenosum in a renal transplant recipient: A case report and review of literature |
title | Pyoderma gangrenosum in a renal transplant recipient: A case report and review of literature |
title_full | Pyoderma gangrenosum in a renal transplant recipient: A case report and review of literature |
title_fullStr | Pyoderma gangrenosum in a renal transplant recipient: A case report and review of literature |
title_full_unstemmed | Pyoderma gangrenosum in a renal transplant recipient: A case report and review of literature |
title_short | Pyoderma gangrenosum in a renal transplant recipient: A case report and review of literature |
title_sort | pyoderma gangrenosum in a renal transplant recipient: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588326/ https://www.ncbi.nlm.nih.gov/pubmed/26628796 http://dx.doi.org/10.4103/0971-4065.156900 |
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