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一名患有21-羟化酶缺乏型先天性肾上腺增生症男性的不育症

Infertility in a man with 21-hydroxylase deficient congenital adrenal hyperplasia.

作者信息

Mirsky H A, Hines J H

机构信息

Department of Surgery, Hamot Medical Center, Erie, Pennsylvania.

出版信息

J Urol. 1989 Jul;142(1):111-3. doi: 10.1016/s0022-5347(17)38677-9.

Abstract

Congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency in men can cause profound oligospermia. The mechanism for this condition is overproduction of adrenal androgens, which in turn inhibit gonadotropin secretion. Men with a mild subclinical form of congenital adrenal hyperplasia may remain undiagnosed until adulthood. We report on a man who presented with infertility secondary to profound oligospermia. The treatment of this condition resulted in improved semen quality and subsequent conception. The importance of family history and determining whether precocious puberty was present, as well as obtaining appropriate laboratory tests is discussed.

摘要

男性因21-羟化酶缺乏所致的先天性肾上腺皮质增生可导致严重少精子症。这种情况的机制是肾上腺雄激素过度产生,进而抑制促性腺激素分泌。患有轻度亚临床型先天性肾上腺皮质增生的男性可能直到成年才被诊断出来。我们报告了一名因严重少精子症导致不育的男性。这种疾病的治疗使精液质量得到改善并随后受孕。文中讨论了家族史的重要性、确定是否存在性早熟以及进行适当实验室检查的重要性。

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