Author:
Bulotta Anna Lavinia,Molinaro Francesco,Angotti Rossella,Ferrara Francesco,Di Maggio Giovanni,Bindi Edoardo,Messina Mario
Abstract
Abstract
Neonatal testicular tumors are rare and should be considered in the differential diagnosis of newborn scrotal masses. Juvenile granulosa cell tumor (JGCT) accounts for about 5% of all prepubertal testis tumors. As a benign neoplasm, radical orchiectomy is sufficient for treatment. We report a case of a newborn with a prenatal diagnosis of scrotal mass. After surgery, the histological diagnosis was juvenile granulosa cell tumor. To date the patient is healthy.
Publisher
Springer Science and Business Media LLC
Reference10 articles.
1. Zugor V, Labanaris AP, Witt J, Seidler A, Weingartner K, Schott E: ongenital Juvenile Granulosa Cell of the Testis in newborn. Anticancer. 2010, 30: 1731-1734.
2. Partalis N, Tzardi M, Barbagadakis S, Sakellaris G: Juvenile Granulosa Cell Tumor Arising From Intra-abdominal Testis in Newborn: Case Report and Review of the Literature. Urology. 2011, 2011: 2011-Article in press
3. Peterson C, Skoog S: Prenatal diagnosis of juvenile granulosa cell tumor of the testis. J Pediatr Urol. 2008, 4: 472-474. 10.1016/j.jpurol.2008.04.005.
4. Canning DA: Congenital juvenile granulosa cell tumor of the testis in newborns. J Urol. 2011, 185: 684-10.1016/S0022-5347(11)60127-4.
5. Shukla AR, Huff DS, Canning DA, Filmer RB, Snyder HM, Carpintieri D, Carr MC: Juvenile granulosa cell tumor of the testis: contemporary clinical management and pathological diagnosis. J Urol. 2004, 171: 1900-1902. 10.1097/01.ju.0000120223.29924.3b.
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