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A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor
Prepubertal gynecomastia due to testis tumors is a very rare condition. Nearly 5% of the patients with testicular mass present with gynecomastia. Sertoli cell tumors are sporadic in 60% of the reported cases, while the remaining is a component of multiple neoplasia syndromes such as Peutz-Jeghers sy...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4561109/ https://www.ncbi.nlm.nih.gov/pubmed/26366315 http://dx.doi.org/10.1155/2015/439239 |
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author | Dursun, Fatma Su Dur, Şeyma Meliha Şahin, Ceyhan Kırmızıbekmez, Heves Karabulut, Murat Hakan Yörük, Asım |
author_facet | Dursun, Fatma Su Dur, Şeyma Meliha Şahin, Ceyhan Kırmızıbekmez, Heves Karabulut, Murat Hakan Yörük, Asım |
author_sort | Dursun, Fatma |
collection | PubMed |
description | Prepubertal gynecomastia due to testis tumors is a very rare condition. Nearly 5% of the patients with testicular mass present with gynecomastia. Sertoli cell tumors are sporadic in 60% of the reported cases, while the remaining is a component of multiple neoplasia syndromes such as Peutz-Jeghers syndrome and Carney complex. We present a 4-year-old boy with gynecomastia due to Sertoli cell tumor with no evidence of Peutz-Jeghers syndrome or Carney complex. |
format | Online Article Text |
id | pubmed-4561109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-45611092015-09-13 A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor Dursun, Fatma Su Dur, Şeyma Meliha Şahin, Ceyhan Kırmızıbekmez, Heves Karabulut, Murat Hakan Yörük, Asım Case Rep Pediatr Case Report Prepubertal gynecomastia due to testis tumors is a very rare condition. Nearly 5% of the patients with testicular mass present with gynecomastia. Sertoli cell tumors are sporadic in 60% of the reported cases, while the remaining is a component of multiple neoplasia syndromes such as Peutz-Jeghers syndrome and Carney complex. We present a 4-year-old boy with gynecomastia due to Sertoli cell tumor with no evidence of Peutz-Jeghers syndrome or Carney complex. Hindawi Publishing Corporation 2015 2015-08-23 /pmc/articles/PMC4561109/ /pubmed/26366315 http://dx.doi.org/10.1155/2015/439239 Text en Copyright © 2015 Fatma Dursun 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 Dursun, Fatma Su Dur, Şeyma Meliha Şahin, Ceyhan Kırmızıbekmez, Heves Karabulut, Murat Hakan Yörük, Asım A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor |
title | A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor |
title_full | A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor |
title_fullStr | A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor |
title_full_unstemmed | A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor |
title_short | A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor |
title_sort | rare cause of prepubertal gynecomastia: sertoli cell tumor |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4561109/ https://www.ncbi.nlm.nih.gov/pubmed/26366315 http://dx.doi.org/10.1155/2015/439239 |
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