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Rare virilizing granulosa cell tumor in an adolescent.
Bús, Dorottya; Buzogány, Mária; Nagy, Gyöngyi; Vajda, György.
Afiliação
  • Bús D; Department of Obstetrics and Gynecology, Zala County Hospital, 8900 Zalaegerszeg, Hungary.
  • Buzogány M; Department of Neonatology and Pediatrics, Zala County Hospital, 8900 Zalaegerszeg, Hungary.
  • Nagy G; Department of Radiology, Zala County Hospital, 8900 Zalaegerszeg, Hungary.
  • Vajda G; Department of Obstetrics and Gynecology, Zala County Hospital, 8900 Zalaegerszeg, Hungary.
Mol Clin Oncol ; 6(1): 88-90, 2017 Jan.
Article em En | MEDLINE | ID: mdl-28123736
ABSTRACT
Hormone-producing malignancies are rare in children or adolescent patients Only 0.1% of all ovarian tumors and 4-5% of granulosa cell tumors occur in the sexually non-active ages. Granulosa cell tumors (GCTs) are sex cord-stromal tumors of the ovary, representing 7-8% of all ovarian neoplasms. A total of 95% of all GCTs are adult-type, and only 5% are diagnosed as juvenile-type GCT. A majority of children with juvenile-type GCT present with isosexual precocious pseudopuberty due to excessive estrogen production, although virilizing, testosterone-producing, juvenile-type GCTs are rare, occurring only in 2-3% of cases. The present case study reports on a case of a virilizing, juvenile-type GCT in a 14-year-old girl, along with a review of the literature.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article