Cover image of the article: Juvenile granulosa cell tumor of the testis in a 3-month-old infant

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Juvenile granulosa cell tumor of the testis in a 3-month-old infant

Authors

N Zabolinejad1,*, Sadegh Sadeghipour Roodsari2, D Omidvartehrani3
1Pathology dept, Faculty of medicine, Mashhad University of Medical Sciences and health services, Mashhad, Iran.
2Pediatric disease Dept, Faculty of Medicine, Mashhad University of Medical Sciences and health services, Mashhad, Iran.
3Assistant of Pathology, Mashhad University of Medical Sciences and health services, Mashhad, Iran.
*Corresponding Author: Pathology dept, Faculty of medicine, Mashhad University of Medical Sciences and health services, Mashhad, Iran. Email: n-zabolinejad@mums.ac.ir

Zahedan Journal of Research in Medical Sciences:Vol. 7, issue 3; e94934
Published online:Sep 20, 2005
Article type:Research Article
Received:May 10, 2005
Accepted:Sep 05, 2005
How to Cite:Zabolinejad N, Sadeghipour Roodsari S, Omidvartehrani D. Juvenile granulosa cell tumor of the testis in a 3-month-old infant. Zahedan J Res Med Sci. 2005;7(3):e94934. doi:

Abstract

Juvenile granulosa cell tumor (JGCT) is a rarely diagnosed subset of benign sex cordstromal
testis tumors. Although it accounts for only 1.2% of all prepubertal testis tumors, the
JGCT is one of the most common congenital and infantile testicular neoplasms. In contrast to
other sex cord-stromal tumors in boys and to the ovarian homologue of the JGCT, there are no
clinically evident endocrine manifestations.
In this article we report a case of juvenile granulosa cell tumor of the left testis in a 3-
month-old infant.

Highlights

Fulltext

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References

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Copyright

© 2005, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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