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Primary Leiomyosarcoma of the Adrenal Gland: A Case Report with Immunohistochemical Study and Literature Review
Primary adrenal leiomyosarcoma is extremely rare tumor. We report a case with adrenal leiomyosarcoma. Our case was a 48-year-old man who presented with lower urinary tract symptoms. Ultrasonography and magnetic resonance imaging revealed approximately 9 cm solid mass originating from right adrenal g...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971559/ https://www.ncbi.nlm.nih.gov/pubmed/24716083 http://dx.doi.org/10.1155/2014/489630 |
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author | Gulpinar, Murat Tolga Yildirim, Asif Gucluer, Berrin Atis, Ramazan Gokhan Canakci, Cengiz Gurbuz, Cenk Caskurlu, Turhan |
author_facet | Gulpinar, Murat Tolga Yildirim, Asif Gucluer, Berrin Atis, Ramazan Gokhan Canakci, Cengiz Gurbuz, Cenk Caskurlu, Turhan |
author_sort | Gulpinar, Murat Tolga |
collection | PubMed |
description | Primary adrenal leiomyosarcoma is extremely rare tumor. We report a case with adrenal leiomyosarcoma. Our case was a 48-year-old man who presented with lower urinary tract symptoms. Ultrasonography and magnetic resonance imaging revealed approximately 9 cm solid mass originating from right adrenal gland. He underwent right adrenalectomy. Pathology of the specimen showed histologic and immunohistochemical features of adrenal leiomyosarcoma. |
format | Online Article Text |
id | pubmed-3971559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-39715592014-04-08 Primary Leiomyosarcoma of the Adrenal Gland: A Case Report with Immunohistochemical Study and Literature Review Gulpinar, Murat Tolga Yildirim, Asif Gucluer, Berrin Atis, Ramazan Gokhan Canakci, Cengiz Gurbuz, Cenk Caskurlu, Turhan Case Rep Urol Case Report Primary adrenal leiomyosarcoma is extremely rare tumor. We report a case with adrenal leiomyosarcoma. Our case was a 48-year-old man who presented with lower urinary tract symptoms. Ultrasonography and magnetic resonance imaging revealed approximately 9 cm solid mass originating from right adrenal gland. He underwent right adrenalectomy. Pathology of the specimen showed histologic and immunohistochemical features of adrenal leiomyosarcoma. Hindawi Publishing Corporation 2014 2014-03-04 /pmc/articles/PMC3971559/ /pubmed/24716083 http://dx.doi.org/10.1155/2014/489630 Text en Copyright © 2014 Murat Tolga Gulpinar 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 Gulpinar, Murat Tolga Yildirim, Asif Gucluer, Berrin Atis, Ramazan Gokhan Canakci, Cengiz Gurbuz, Cenk Caskurlu, Turhan Primary Leiomyosarcoma of the Adrenal Gland: A Case Report with Immunohistochemical Study and Literature Review |
title | Primary Leiomyosarcoma of the Adrenal Gland: A Case Report with Immunohistochemical Study and Literature Review |
title_full | Primary Leiomyosarcoma of the Adrenal Gland: A Case Report with Immunohistochemical Study and Literature Review |
title_fullStr | Primary Leiomyosarcoma of the Adrenal Gland: A Case Report with Immunohistochemical Study and Literature Review |
title_full_unstemmed | Primary Leiomyosarcoma of the Adrenal Gland: A Case Report with Immunohistochemical Study and Literature Review |
title_short | Primary Leiomyosarcoma of the Adrenal Gland: A Case Report with Immunohistochemical Study and Literature Review |
title_sort | primary leiomyosarcoma of the adrenal gland: a case report with immunohistochemical study and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971559/ https://www.ncbi.nlm.nih.gov/pubmed/24716083 http://dx.doi.org/10.1155/2014/489630 |
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