Diagnóstico prenatal de tumor de células de la granulosa de tipo juvenil
González B., Isabel ; Tejero C., Eva Lucía ; Marquina I. , Isabel ; Lerma P., Diego ; Rojas PE., Beatriz ; Pérez P., Pilar (Universidad de Zaragoza)
Resumen: Presentamos un caso clínico de diagnóstico prenatal de una masa testicular. Tras el nacimiento, se realizó la exéresis del tumor y el análisis anatomopatológico determinó que se trataba de un tumor de células de la granulosa juvenil. Los tumores testiculares son raros y deben considerarse en el diagnóstico diferencial de las masas escrotales en los neonatos. El tumor de células de la granulosa juvenil es una entidad clínico-patológica poco frecuente, que representa el 5% de los tumores testiculares prepuberales. Se considera una neoplasia benigna y la orquiectomía es una técnica quirúrgica curativa.
We report a case of a prenatally diagnosed testis tumor. After delivery, it was decided to perform right radical orchiectomy which was subsequently diagnosed as a juvenile granulosa cell tumor. Neonatal testicular tumors are rare and should be considered in the differential diagnosis of newborn scrotal masses. Juvenile granulosa cell tumor is a rare benign neoplasm of the testicular stroma that accounts for 5% of all prepuberal testis tumors. As a benign neoplasm, orchiectomy is sufficient for treatment.
Idioma: Español
Año: 2015
Publicado en: Revista Chilena de Obstetricia y Ginecologia 80, 3 (2015), 251-255
ISSN: 0048-766X
Originalmente disponible en: Texto completo de la revista
Factor impacto SCIMAGO: 0.119 - Obstetrics and Gynecology (Q4)
Tipo y forma: Article (Published version)
Área (Departamento): Área Obstetricia y Ginecología (Dpto. Cirugía,Ginecol.Obstetr.)
You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use. You may not use the material for commercial purposes.
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We report a case of a prenatally diagnosed testis tumor. After delivery, it was decided to perform right radical orchiectomy which was subsequently diagnosed as a juvenile granulosa cell tumor. Neonatal testicular tumors are rare and should be considered in the differential diagnosis of newborn scrotal masses. Juvenile granulosa cell tumor is a rare benign neoplasm of the testicular stroma that accounts for 5% of all prepuberal testis tumors. As a benign neoplasm, orchiectomy is sufficient for treatment.
Idioma: Español
Año: 2015
Publicado en: Revista Chilena de Obstetricia y Ginecologia 80, 3 (2015), 251-255
ISSN: 0048-766X
Originalmente disponible en: Texto completo de la revista
Factor impacto SCIMAGO: 0.119 - Obstetrics and Gynecology (Q4)
Tipo y forma: Article (Published version)
Área (Departamento): Área Obstetricia y Ginecología (Dpto. Cirugía,Ginecol.Obstetr.)
You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use. You may not use the material for commercial purposes. Exportado de SIDERAL (2021-01-21-11:14:48)
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Record created 2017-09-11, last modified 2021-01-21