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Penile pyoderma gangrenosum successfully treated with topical Imiquimod

Pyoderma gangrenosum(PG) is a rare ulcerating inflammatory neutrophilic dermatosis. Genital involvement has been rarely reported. We report such a case of 24- year- old, male patient living with HIV/AIDS(PLHIV) who presented with progressive genital ulceration, not responding to oral antibiotics and...

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Autores principales: Rathod, Santosh P., Padhiar, Bela B., Karia, Umesh K., Shah, Bela J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195173/
https://www.ncbi.nlm.nih.gov/pubmed/22021975
http://dx.doi.org/10.4103/2589-0557.85418
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author Rathod, Santosh P.
Padhiar, Bela B.
Karia, Umesh K.
Shah, Bela J.
author_facet Rathod, Santosh P.
Padhiar, Bela B.
Karia, Umesh K.
Shah, Bela J.
author_sort Rathod, Santosh P.
collection PubMed
description Pyoderma gangrenosum(PG) is a rare ulcerating inflammatory neutrophilic dermatosis. Genital involvement has been rarely reported. We report such a case of 24- year- old, male patient living with HIV/AIDS(PLHIV) who presented with progressive genital ulceration, not responding to oral antibiotics and aciclovir, gradually increasing in size over 15-18 months. Repeated biopsies showed acute on chronic inflammation. The lesion partially responded to oral and topical corticosteroids but soon increased in size after tapering the dosage of the steroids.Then patient was given Imiquimod 5% cream to be applied over the lesion once daily for 2-4 weeks. Lesion cleared completely in 4 weeks and is in remission since last 6 months. The case report highlights the successful use of topical Imiquimod 5% cream in the treatment of penile PG.
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spelling pubmed-31951732011-10-21 Penile pyoderma gangrenosum successfully treated with topical Imiquimod Rathod, Santosh P. Padhiar, Bela B. Karia, Umesh K. Shah, Bela J. Indian J Sex Transm Dis AIDS Case Report Pyoderma gangrenosum(PG) is a rare ulcerating inflammatory neutrophilic dermatosis. Genital involvement has been rarely reported. We report such a case of 24- year- old, male patient living with HIV/AIDS(PLHIV) who presented with progressive genital ulceration, not responding to oral antibiotics and aciclovir, gradually increasing in size over 15-18 months. Repeated biopsies showed acute on chronic inflammation. The lesion partially responded to oral and topical corticosteroids but soon increased in size after tapering the dosage of the steroids.Then patient was given Imiquimod 5% cream to be applied over the lesion once daily for 2-4 weeks. Lesion cleared completely in 4 weeks and is in remission since last 6 months. The case report highlights the successful use of topical Imiquimod 5% cream in the treatment of penile PG. Medknow Publications 2011 /pmc/articles/PMC3195173/ /pubmed/22021975 http://dx.doi.org/10.4103/2589-0557.85418 Text en Copyright: © Indian Journal of Sexually Transmitted Diseases and AIDS 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Rathod, Santosh P.
Padhiar, Bela B.
Karia, Umesh K.
Shah, Bela J.
Penile pyoderma gangrenosum successfully treated with topical Imiquimod
title Penile pyoderma gangrenosum successfully treated with topical Imiquimod
title_full Penile pyoderma gangrenosum successfully treated with topical Imiquimod
title_fullStr Penile pyoderma gangrenosum successfully treated with topical Imiquimod
title_full_unstemmed Penile pyoderma gangrenosum successfully treated with topical Imiquimod
title_short Penile pyoderma gangrenosum successfully treated with topical Imiquimod
title_sort penile pyoderma gangrenosum successfully treated with topical imiquimod
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195173/
https://www.ncbi.nlm.nih.gov/pubmed/22021975
http://dx.doi.org/10.4103/2589-0557.85418
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