[精原细胞瘤与肾上腺生殖综合征]
[Seminoma and adrenogenital syndrome].
作者信息
Santoro G, Nacchia F, Rocco P
机构信息
Divisione di Chirurgia Generale, Universitá degli Studi Federico II, Napoli.
出版信息
G Chir. 1998 Aug-Sep;19(8-9):338-40.
PMID:9734185
Abstract
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.
摘要
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）。
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