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Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature
Adult testicular granulosa cell tumors are rare sex cord- stromal tumors of which only 45 have been previously reported. As compared with their ovarian counterparts, these tumors may follow a more aggressive course because the proportion of malignant cases is higher. We report here a unique case of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4100032/ https://www.ncbi.nlm.nih.gov/pubmed/24894598 http://dx.doi.org/10.1186/1746-1596-9-107 |
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author | Schubert, Thomas EO Stoehr, Robert Hartmann, Arndt Schöne, Sabrina Löbelenz, Mathias Mikuz, Gregor |
author_facet | Schubert, Thomas EO Stoehr, Robert Hartmann, Arndt Schöne, Sabrina Löbelenz, Mathias Mikuz, Gregor |
author_sort | Schubert, Thomas EO |
collection | PubMed |
description | Adult testicular granulosa cell tumors are rare sex cord- stromal tumors of which only 45 have been previously reported. As compared with their ovarian counterparts, these tumors may follow a more aggressive course because the proportion of malignant cases is higher. We report here a unique case of a 78-year Caucasian with a left sided adult type granulosa cell tumor with a heterologous sarcomatous tumor component. A heterologous sarcomatous component has occasionally been observed in ovarian tumors but never in testicular granulosa cell tumors. The sarcomatous component showed a higher number of mitotic figures (1/Hpf) and a marked proliferation rate (up to 50% Ki 67 positive cells) compared with the granulosa type tumor component. CD 99 and the progesterone receptor were positive in both tumor components, inhibin and calretinin only in the granulosa cells, and pancytokeratin only in the sarcomatouse one. Key words: testis - ovary - granulosa cells - sarcoma - inhibin Runing title: testicular sarcomatous granulosa tumor. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/6959043481207016 |
format | Online Article Text |
id | pubmed-4100032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41000322014-07-17 Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature Schubert, Thomas EO Stoehr, Robert Hartmann, Arndt Schöne, Sabrina Löbelenz, Mathias Mikuz, Gregor Diagn Pathol Case Report Adult testicular granulosa cell tumors are rare sex cord- stromal tumors of which only 45 have been previously reported. As compared with their ovarian counterparts, these tumors may follow a more aggressive course because the proportion of malignant cases is higher. We report here a unique case of a 78-year Caucasian with a left sided adult type granulosa cell tumor with a heterologous sarcomatous tumor component. A heterologous sarcomatous component has occasionally been observed in ovarian tumors but never in testicular granulosa cell tumors. The sarcomatous component showed a higher number of mitotic figures (1/Hpf) and a marked proliferation rate (up to 50% Ki 67 positive cells) compared with the granulosa type tumor component. CD 99 and the progesterone receptor were positive in both tumor components, inhibin and calretinin only in the granulosa cells, and pancytokeratin only in the sarcomatouse one. Key words: testis - ovary - granulosa cells - sarcoma - inhibin Runing title: testicular sarcomatous granulosa tumor. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/6959043481207016 BioMed Central 2014-06-03 /pmc/articles/PMC4100032/ /pubmed/24894598 http://dx.doi.org/10.1186/1746-1596-9-107 Text en Copyright © 2014 Schubert et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Schubert, Thomas EO Stoehr, Robert Hartmann, Arndt Schöne, Sabrina Löbelenz, Mathias Mikuz, Gregor Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature |
title | Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature |
title_full | Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature |
title_fullStr | Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature |
title_full_unstemmed | Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature |
title_short | Adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature |
title_sort | adult type granulosa cell tumor of the testis with a heterologous sarcomatous component: case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4100032/ https://www.ncbi.nlm.nih.gov/pubmed/24894598 http://dx.doi.org/10.1186/1746-1596-9-107 |
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