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Prepubertal testicular tumors: Our 10 years experience.
Indian J Cancer ; 2010 Jul-Sept; 47(3): 292-295
Artículo en Inglés | IMSEAR | ID: sea-144353
ABSTRACT

Background:

Testicular tumors in the pediatric population are distinct from those of the adults. In contrast to the prevalence data reported in tumor registries, several studies have shown that a majority of the prepubertal testis tumors are benign. We retrospectively analyzed a series of prepubertal testicular tumors. Materials and

Methods:

A retrospective review of all testicular tumors at our institution was done from Jan 1999 to Dec 2008. Data relating to presentation, evaluation, and management were collected.

Results:

A total of 22 children with prepubertal testicular tumors were identified. The mean age at presentation was 4.6 years. Mature teratoma, epidermoid cysts, immature teratoma, and yolk sac tumor accounted for 49.94%, 13.62%, 9.08%, and 18.16%, respectively. All surgeries were successful with respect to cancer control and testicular preservation.

Conclusions:

Benign tumors formed the majority (72.64%) of the tumors that were encountered, with yolk sac tumors (18.16%) being a minority. Testicular preserving surgery appears to be a feasible option for benign tumors and is safe and efficacious in long-term follow-up.
Asunto(s)

Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Asunto principal: Teratoma / Neoplasias Testiculares / Humanos / Masculino / Orquiectomía / Niño / Preescolar / Estudios Retrospectivos / Estudios de Seguimiento / Pubertad Tipo de estudio: Estudio observacional / Estudio pronóstico / Factores de riesgo Idioma: Inglés Revista: Indian J Cancer Año: 2010 Tipo del documento: Artículo

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Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Asunto principal: Teratoma / Neoplasias Testiculares / Humanos / Masculino / Orquiectomía / Niño / Preescolar / Estudios Retrospectivos / Estudios de Seguimiento / Pubertad Tipo de estudio: Estudio observacional / Estudio pronóstico / Factores de riesgo Idioma: Inglés Revista: Indian J Cancer Año: 2010 Tipo del documento: Artículo