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混合性性腺发育不全与发育异常性男性假两性畸形——批判性分析

Mixed gonadal dysgenesis and dysgenetic male pseudohermaphroditism--a critical analysis.

作者信息

Rohatgi M, Gupta D K, Menon P S, Verma I C, Mathur M

机构信息

Department of Pediatric Surgery, All India Institute of Medical Sciences, New Delhi.

出版信息

Indian J Pediatr. 1992 Jul-Aug;59(4):487-500. doi: 10.1007/BF02751566.

Abstract

A 10 year prospective study of 14 patients with mixed gonadal dysgenesis (MGD) and six patients with dysgenetic male pseudohermaphroditism (DMP) is reported. All of them had internal mullerian structures, along with unilateral or bilateral dysgenetic testes, ambiguous external genitalia. Twelve had been brought up as male, nine of whom had a unilateral descended testis. Eight had been reared as females, as they had bilaterally undescended gonads, and ambiguous genitalia. Clinical examination, retrograde genito-urethrography and cytogenetic studies suggested the diagnosis in 16 patients, while four were diagnosed on inguino-abdominal exploration for undescended testis. This report delineates more clearly the clinical profile of these orders. All the patients reared as male were assigned the male gender following abdominal gonadectomy, retention of scrotal testis and male genitoplasty. The eight patients who were reared as females underwent bilateral salpingo-gonadectomy and female genitoplasty. This management differs from the usual recommendation that all such children should be reared as females. Ten patients (50%) had maternal history of previous abortion/stillbirth, or drug intake in the first trimester of pregnancy suggesting a role of these factors in the etiology. All cases of DMP had a 46,XY karyotype, while eight of 14 cases of MGD had mosaicism with 45X/46,XY cell lines in blood or gonadal cultures. The clinicopathological features of patients of MGD and DMP were similar. It is suggested that these two disorders represent different spectra of the same disorder. A unifying concept of etiopathogenesis is proposed.

摘要

本文报道了一项针对14例混合性性腺发育不全(MGD)患者和6例发育异常男性假两性畸形(DMP)患者的10年前瞻性研究。所有患者均有内苗勒氏结构,伴有单侧或双侧发育异常的睾丸及外生殖器模糊不清。其中12例自幼被当作男性抚养,9例有单侧睾丸下降。8例自幼被当作女性抚养,因其双侧性腺未降且生殖器模糊不清。临床检查、逆行性泌尿生殖造影及细胞遗传学研究确诊了16例患者,另外4例因隐睾而行腹股沟-腹部探查时确诊。本报告更清晰地描绘了这些病症的临床特征。所有自幼被当作男性抚养的患者在接受腹部性腺切除、保留阴囊内睾丸及男性生殖器成形术后仍被指定为男性性别。8例自幼被当作女性抚养的患者接受了双侧输卵管-性腺切除术及女性生殖器成形术。这种治疗方法与通常建议所有此类儿童都应被当作女性抚养的观点不同。10例患者(50%)有母亲既往流产/死产史或孕期头三个月用药史,提示这些因素在病因学中起作用。所有DMP病例的核型均为46,XY,而14例MGD病例中有8例在血液或性腺培养中有45X/46,XY细胞系的嵌合体。MGD和DMP患者的临床病理特征相似。提示这两种病症代表了同一病症的不同谱系。提出了一个病因发病机制的统一概念。

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