Subcutaneous Leiomyosarcoma of the Frenulum

Leiomyosarcomas of the penis are rare, with only 29 reported cases to date. We record the case of a patient who presented with a 2-year history of a seemingly indolent penile skin lesion. On histopathology of the local resection, a diagnosis of subcutaneous leiomyosarcoma was made. Specifically, lei...

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Main Authors: D. Mendis, S. R. J. Bott, J. H. Davies
Format: Article
Language:English
Published: Wiley 2005-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/tsw.2005.76
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author D. Mendis
S. R. J. Bott
J. H. Davies
author_facet D. Mendis
S. R. J. Bott
J. H. Davies
author_sort D. Mendis
collection DOAJ
description Leiomyosarcomas of the penis are rare, with only 29 reported cases to date. We record the case of a patient who presented with a 2-year history of a seemingly indolent penile skin lesion. On histopathology of the local resection, a diagnosis of subcutaneous leiomyosarcoma was made. Specifically, leiomyosarcoma of the penile frenulum has not been clearly reported previously. The patient underwent a further excision to ensure an adequate resection margin and has had no disease recurrence at subsequent follow-up. Our case was of a lesion that, although clinically benign, was malignant and this possibility should be borne in mind when assessing patients.
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spelling doaj-art-3dc0e56d27d542ec80fa4410b80b2ce92025-02-03T06:08:31ZengWileyThe Scientific World Journal1537-744X2005-01-01557157510.1100/tsw.2005.76Subcutaneous Leiomyosarcoma of the FrenulumD. Mendis0S. R. J. Bott1J. H. Davies2Department of Urology, Royal Surrey County Hospital NHS Trust, UKDepartment of Urology, Royal Surrey County Hospital NHS Trust, UKDepartment of Urology, Royal Surrey County Hospital NHS Trust, UKLeiomyosarcomas of the penis are rare, with only 29 reported cases to date. We record the case of a patient who presented with a 2-year history of a seemingly indolent penile skin lesion. On histopathology of the local resection, a diagnosis of subcutaneous leiomyosarcoma was made. Specifically, leiomyosarcoma of the penile frenulum has not been clearly reported previously. The patient underwent a further excision to ensure an adequate resection margin and has had no disease recurrence at subsequent follow-up. Our case was of a lesion that, although clinically benign, was malignant and this possibility should be borne in mind when assessing patients.http://dx.doi.org/10.1100/tsw.2005.76
spellingShingle D. Mendis
S. R. J. Bott
J. H. Davies
Subcutaneous Leiomyosarcoma of the Frenulum
The Scientific World Journal
title Subcutaneous Leiomyosarcoma of the Frenulum
title_full Subcutaneous Leiomyosarcoma of the Frenulum
title_fullStr Subcutaneous Leiomyosarcoma of the Frenulum
title_full_unstemmed Subcutaneous Leiomyosarcoma of the Frenulum
title_short Subcutaneous Leiomyosarcoma of the Frenulum
title_sort subcutaneous leiomyosarcoma of the frenulum
url http://dx.doi.org/10.1100/tsw.2005.76
work_keys_str_mv AT dmendis subcutaneousleiomyosarcomaofthefrenulum
AT srjbott subcutaneousleiomyosarcomaofthefrenulum
AT jhdavies subcutaneousleiomyosarcomaofthefrenulum