作者: FJ Cameron , I Scheimberg , R Stanhope
DOI: 10.1111/J.1651-2227.1997.TB15193.X
关键词:
摘要: We describe a juvenile granulosa cell tumour resulting in pseudopuberty an infant female. The progression of the clinical signs puberty were non-consonant and diagnosis was complicated by marginally elevated serum α-fetoprotein levels. histological appearance resected binding MIC2 antibody to cells confirmed diagnosis.