Bús Dorottya, Buzogány Mária, Nagy Gyöngyi, Vajda György
Department of Obstetrics and Gynecology, Zala County Hospital, 8900 Zalaegerszeg, Hungary.
Department of Neonatology and Pediatrics, Zala County Hospital, 8900 Zalaegerszeg, Hungary.
Mol Clin Oncol. 2017 Jan;6(1):88-90. doi: 10.3892/mco.2016.1084. Epub 2016 Nov 18.
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.
在所有卵巢肿瘤中,仅有0.1%发生于性未发育活跃期,而颗粒细胞瘤中这一比例为4 - 5%。颗粒细胞瘤(GCTs)是卵巢性索间质肿瘤,占所有卵巢肿瘤的7 - 8%。所有GCTs中95%为成人型,仅5%被诊断为青少年型GCT。大多数青少年型GCT患儿因雌激素分泌过多而出现同性性早熟假性青春期,不过,分泌雄激素、导致男性化的青少年型GCT较为罕见,仅占病例的2 - 3%。本病例研究报告了一名14岁女孩发生的男性化青少年型GCT病例,并对相关文献进行了综述。