Santoro G, Nacchia F, Rocco P
Divisione di Chirurgia Generale, Universitá degli Studi Federico II, Napoli.
G Chir. 1998 Aug-Sep;19(8-9):338-40.
The Authors report a case of a 26 year old patient affected by adrenogenital syndrome, likely due to 21 hydroxylase defect, hermaphroditism (46XX genotype and female phenotype) and worked hyperandrogenism; moreover a hidden testis neoplasm (seminoma) was associated.
作者报告了一例26岁患者，患有肾上腺生殖器综合征，可能由于21-羟化酶缺陷所致，表现为两性畸形（46XX基因型和女性表型）及功能性高雄激素血症；此外，还伴有隐匿性睾丸肿瘤（精原细胞瘤）。
