Cargando…
Recurrent furunculosis as a cause of isolated penile lymphedema: a case report
INTRODUCTION: Isolated lymphedema of the penis is extremely rare: combined involvement of the scrotum and penis is the norm. Furunculosis as a cause is not, to our knowledge, previously reported. We present a case of isolated penile lymphedema that responded to excision of lymphedematous tissue and...
Autores principales: | , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902497/ https://www.ncbi.nlm.nih.gov/pubmed/20584337 http://dx.doi.org/10.1186/1752-1947-4-196 |
_version_ | 1782183773069115392 |
---|---|
author | Al-shaham, Ali A Sood, Suneet |
author_facet | Al-shaham, Ali A Sood, Suneet |
author_sort | Al-shaham, Ali A |
collection | PubMed |
description | INTRODUCTION: Isolated lymphedema of the penis is extremely rare: combined involvement of the scrotum and penis is the norm. Furunculosis as a cause is not, to our knowledge, previously reported. We present a case of isolated penile lymphedema that responded to excision of lymphedematous tissue and reconstruction with flaps. CASE PRESENTATION: A 32-year-old Arab man presented with a three-year history of a gradually increasing, painless penile swelling. Our patient's main complaint was non-erectile sexual dysfunction. The swelling was preceded by at least three prior episodes of severe furunculosis at the penile root. He had no other contributory past medical or family history. On examination there was gross penile enlargement, maximally at the mid shaft, associated with thickened skin at the sites of prior furunculosis. The glans and scrotum were normal. Both testes were palpable. Serology for filariasis, and urinary tract ultrasound and computed tomography scan were normal. The clinical diagnosis was lymphedema following recurrent penile furunculosis. At operation the lymphedematous tissues were removed. Closure of the penile shaft was accomplished by bilateral advancement of flaps from both ends of the penis. He resumed normal sexual activity one month after surgery. At 12 months, he had a good cosmetic result, with no signs of recurrence. CONCLUSIONS: Furunculosis at the penile root may result in lymphedema confined to the penile shaft, sparing the scrotum. Excision of abnormal tissue and cover with a skin flap gave excellent cosmetic results, and allowed satisfactory sexual activity. |
format | Text |
id | pubmed-2902497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29024972010-07-13 Recurrent furunculosis as a cause of isolated penile lymphedema: a case report Al-shaham, Ali A Sood, Suneet J Med Case Reports Case report INTRODUCTION: Isolated lymphedema of the penis is extremely rare: combined involvement of the scrotum and penis is the norm. Furunculosis as a cause is not, to our knowledge, previously reported. We present a case of isolated penile lymphedema that responded to excision of lymphedematous tissue and reconstruction with flaps. CASE PRESENTATION: A 32-year-old Arab man presented with a three-year history of a gradually increasing, painless penile swelling. Our patient's main complaint was non-erectile sexual dysfunction. The swelling was preceded by at least three prior episodes of severe furunculosis at the penile root. He had no other contributory past medical or family history. On examination there was gross penile enlargement, maximally at the mid shaft, associated with thickened skin at the sites of prior furunculosis. The glans and scrotum were normal. Both testes were palpable. Serology for filariasis, and urinary tract ultrasound and computed tomography scan were normal. The clinical diagnosis was lymphedema following recurrent penile furunculosis. At operation the lymphedematous tissues were removed. Closure of the penile shaft was accomplished by bilateral advancement of flaps from both ends of the penis. He resumed normal sexual activity one month after surgery. At 12 months, he had a good cosmetic result, with no signs of recurrence. CONCLUSIONS: Furunculosis at the penile root may result in lymphedema confined to the penile shaft, sparing the scrotum. Excision of abnormal tissue and cover with a skin flap gave excellent cosmetic results, and allowed satisfactory sexual activity. BioMed Central 2010-06-29 /pmc/articles/PMC2902497/ /pubmed/20584337 http://dx.doi.org/10.1186/1752-1947-4-196 Text en Copyright ©2010 Al-shaham and Sood; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case report Al-shaham, Ali A Sood, Suneet Recurrent furunculosis as a cause of isolated penile lymphedema: a case report |
title | Recurrent furunculosis as a cause of isolated penile lymphedema: a case report |
title_full | Recurrent furunculosis as a cause of isolated penile lymphedema: a case report |
title_fullStr | Recurrent furunculosis as a cause of isolated penile lymphedema: a case report |
title_full_unstemmed | Recurrent furunculosis as a cause of isolated penile lymphedema: a case report |
title_short | Recurrent furunculosis as a cause of isolated penile lymphedema: a case report |
title_sort | recurrent furunculosis as a cause of isolated penile lymphedema: a case report |
topic | Case report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902497/ https://www.ncbi.nlm.nih.gov/pubmed/20584337 http://dx.doi.org/10.1186/1752-1947-4-196 |
work_keys_str_mv | AT alshahamalia recurrentfurunculosisasacauseofisolatedpenilelymphedemaacasereport AT soodsuneet recurrentfurunculosisasacauseofisolatedpenilelymphedemaacasereport |