A very rare case of adult-type granulosa cell tumor


Submitted: April 1, 2015
Accepted: April 1, 2015
Published: March 31, 2015
Abstract Views: 1633
PDF: 1078
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Authors

Granulosa cell tumor (GST) of the testis is a rare neoplasm. Here we describe a case of an adult type GST. More than a year after surgical treatment, without any other treatment, the patient is alive without sign of disease.

Giulianelli, R., Mirabile, G., Vincenti, G., Pellegrino, F., & Soda, G. (2015). A very rare case of adult-type granulosa cell tumor. Archivio Italiano Di Urologia E Andrologia, 87(1), 98–99. https://doi.org/10.4081/aiua.2015.1.98

Downloads

Download data is not yet available.

Citations