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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...

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Detalles Bibliográficos
Autores principales: Jha, P. K., Rana, A., Kapoor, S., Kher, V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
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.
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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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