Sheth F J, Multani A S, Sheth J J, Radhakrishna U, Shah V C, Chinoy N J
Genetic Centre, Ahmedabad, India.
Urol Int. 1996;56(1):57-60. doi: 10.1159/000282812.
A 21-year-old phenotypic male with ambiguous external genitalia and hypospadias was referred for cytogenetic studies. Exploratory laparotomy revealed presence of a small atropic uterus, unilateral gonadal dysgenesis with fallopian tubes on both sides and a cryptorchid testis on the left side. No gonad could be traced on the right side. Chromosomal analysis from peripheral whole blood culture revealed a 46,XY cell line. No mosaicism was detected. Endocrine studies showed elevated levels of serum FSH and LH with low borderline testosterone level and failure to respond to HCG stimulation. The presence of fallopian tube next to testis suggests absence of anti-Mullerian hormone secretion by Sertoli cells. The absence of Wolffian duct derivatives indicates insufficient secretion of testosterone by Leydig cells.
一名21岁的表型男性,外生殖器模糊且患有尿道下裂,被转诊进行细胞遗传学研究。 exploratory laparotomy显示存在一个小的萎缩子宫、单侧性腺发育不全伴双侧输卵管以及左侧隐睾。右侧未发现性腺。外周全血培养的染色体分析显示有46,XY细胞系。未检测到嵌合体。内分泌研究显示血清FSH和LH水平升高,睾酮水平处于低临界值且对HCG刺激无反应。睾丸旁存在输卵管提示支持细胞缺乏抗苗勒管激素分泌。中肾管衍生物的缺失表明睾丸间质细胞分泌的睾酮不足。