Juvenile Granulosa Cell Tumor Arising in Undescended Testis: A case report
Korean Journal of Pathology
;
: 376-379, 1999.
Artigo
em Coreano
| WPRIM
| ID: wpr-178206
ABSTRACT
Juvenile granulosa cell tumor is rare but one of the common congenital testicular neoplasms. Although histological features are typical of its ovarian counterpart, testicular juvenile granulosa cell tumor has a distinctly different clinical presentation. We report a case of juvenile granulosa cell tumor arising in the cryptochid testis of a 4-day-old newborn. A 6 5 5 cm sized multilocular cyst containing thick, mucinous fluid was found in the peritoneal cavity. The external surface of the cyst was smooth and the septae were relatively thin. The cyst consisted of numerous mucin-filled, cystic follicles lined by cells having vacuolated cytoplasm and round to oval dark nuclei without grooves. Cells resembling granulosa cells of an ovarian follicle were also observed in the intervening stroma forming irregular solid nests.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Cavidade Peritoneal
/
Neoplasias Testiculares
/
Testículo
/
Criptorquidismo
/
Citoplasma
/
Folículo Ovariano
/
Tumor de Células da Granulosa
/
Células da Granulosa
/
Mucinas
Limite:
Feminino
/
Humanos
/
Masculino
/
Recém-Nascido
Idioma:
Coreano
Revista:
Korean Journal of Pathology
Ano de publicação:
1999
Tipo de documento:
Artigo
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