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Cellular Angiofibroma of the Prostate: A Rare Tumor in an Unusual Location

We report the unusual occurrence of a cellular angiofibroma in prostatic tissue. In this case, a 84-year-old man presented in the emergency room with urinary retention. Ultrasound revealed an enlarged prostate, which was suggestive for benign prostatic hyperplasia. The patient was treated with a Mil...

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Autores principales: Wyn, Inez, Debiec-Rychter, Maria, Van Cleynenbreugel, Ben, Sciot, Raf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102028/
https://www.ncbi.nlm.nih.gov/pubmed/25105048
http://dx.doi.org/10.1155/2014/871530
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author Wyn, Inez
Debiec-Rychter, Maria
Van Cleynenbreugel, Ben
Sciot, Raf
author_facet Wyn, Inez
Debiec-Rychter, Maria
Van Cleynenbreugel, Ben
Sciot, Raf
author_sort Wyn, Inez
collection PubMed
description We report the unusual occurrence of a cellular angiofibroma in prostatic tissue. In this case, a 84-year-old man presented in the emergency room with urinary retention. Ultrasound revealed an enlarged prostate, which was suggestive for benign prostatic hyperplasia. The patient was treated with a Millin retropubic prostatectomy. Macroscopically the prostate contained multiple circumscribed nodules. Microscopic examination of the tumor showed the appearance of cellular angiofibroma, consisting of bland spindle cells and prominent, hyalinized vessels. The diagnosis was supported by FISH, which revealed monoallelic loss of RB1/13q14 region, as seen in spindle cell lipoma, (extra-) mammary myofibroblastoma, and cellular angiofibroma. Cellular angiofibromas are rare, benign soft tissue tumours and were never reported in the prostatic gland.
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spelling pubmed-41020282014-08-07 Cellular Angiofibroma of the Prostate: A Rare Tumor in an Unusual Location Wyn, Inez Debiec-Rychter, Maria Van Cleynenbreugel, Ben Sciot, Raf Case Rep Pathol Case Report We report the unusual occurrence of a cellular angiofibroma in prostatic tissue. In this case, a 84-year-old man presented in the emergency room with urinary retention. Ultrasound revealed an enlarged prostate, which was suggestive for benign prostatic hyperplasia. The patient was treated with a Millin retropubic prostatectomy. Macroscopically the prostate contained multiple circumscribed nodules. Microscopic examination of the tumor showed the appearance of cellular angiofibroma, consisting of bland spindle cells and prominent, hyalinized vessels. The diagnosis was supported by FISH, which revealed monoallelic loss of RB1/13q14 region, as seen in spindle cell lipoma, (extra-) mammary myofibroblastoma, and cellular angiofibroma. Cellular angiofibromas are rare, benign soft tissue tumours and were never reported in the prostatic gland. Hindawi Publishing Corporation 2014 2014-07-01 /pmc/articles/PMC4102028/ /pubmed/25105048 http://dx.doi.org/10.1155/2014/871530 Text en Copyright © 2014 Inez Wyn et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Wyn, Inez
Debiec-Rychter, Maria
Van Cleynenbreugel, Ben
Sciot, Raf
Cellular Angiofibroma of the Prostate: A Rare Tumor in an Unusual Location
title Cellular Angiofibroma of the Prostate: A Rare Tumor in an Unusual Location
title_full Cellular Angiofibroma of the Prostate: A Rare Tumor in an Unusual Location
title_fullStr Cellular Angiofibroma of the Prostate: A Rare Tumor in an Unusual Location
title_full_unstemmed Cellular Angiofibroma of the Prostate: A Rare Tumor in an Unusual Location
title_short Cellular Angiofibroma of the Prostate: A Rare Tumor in an Unusual Location
title_sort cellular angiofibroma of the prostate: a rare tumor in an unusual location
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102028/
https://www.ncbi.nlm.nih.gov/pubmed/25105048
http://dx.doi.org/10.1155/2014/871530
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