Zäh W, Kalderon A E, Tucci J R
Acta Endocrinol Suppl (Copenh). 1975;197:1-39.
Mixed gonadal dysgenesis (MCG) is a rare intersexual disorder, characterized in most cases by the presence of a testis and a contralateral streak gonad; in some cases the contralateral gonad may be rudimentary not having differentiated into an ovary or into a testis and in other cases it may be absent. A personal case was recently studied by the authors in some detail: A 51-year-old individual reared as a female with primary amenorrhea, short stature, subnormal intelligence, male type habitus, hirsutism, moderate breast development, ambiguous external genitalia with a 5 x 2 cm phallus, labia majora with scrotal type skin, and a urogenital sinus. Internal genitalia consisted of a hypoplastic vagina and uterus, a streak gonad on the right and intraabdominal testis, fallopian tube, and epididymis on the left side. The dysgenetic testis contained a gonadoblastoma and the streak a gonadoblastoma and dysgerminoma. A buccal smear was chromatin negative and karyotype analysis revealed XO/XY mosaicism. Thyroid and adrenocortical function was normal. A plasma testosterone level of 0.15 mu-g% rose to 0.45 mu-g% with 3 days of HCG administration. With bilateral gonadectomy the plasma testosterone level fell to 0.06 mu-g% and there was no response following HCG administration. 109 cases of MGD and 2 cases of unilateral gonadal dysgenesis reported in the world literature between 1937 and 1973 were reviewed. On the basis of their clinical and pathological features, the latter two patients were excluded from the category of MGD. In 15 of the 109 cases of MGD, a gonadoblastoma obscuring the gonad of origin was opposed by a dysgenetic gonad with or without a gonadoblastoma or no gonad. In these cases the presence of a testis was not proven histologically and their clinical-pathological features were similar to those found in pure gonadal dysgenesis. Of the remaining 94 cases of MGD, 72 had testicular tissue on one side and a streak or embryonic gonad on the other while 22 had a testis and no contralateral gonad...
混合性性腺发育不全(MCG)是一种罕见的两性畸形疾病,多数情况下其特征为一侧有睾丸,对侧为条索状性腺;某些情况下,对侧性腺可能发育不全,未分化为卵巢或睾丸,还有些情况则可能完全缺失。作者最近详细研究了一个个案:一名51岁个体,自幼被当作女性抚养,有原发性闭经、身材矮小、智力发育不全、男性体型、多毛、乳房中度发育、外生殖器模糊,有一个5×2厘米的阴茎,大阴唇有阴囊样皮肤,还有一个泌尿生殖窦。内生殖器包括发育不全的阴道和子宫,右侧为条索状性腺,左侧为腹腔内睾丸、输卵管和附睾。发育异常的睾丸中有一个性腺母细胞瘤,条索状性腺中有一个性腺母细胞瘤和无性细胞瘤。口腔涂片染色质阴性,染色体核型分析显示为XO/XY嵌合体。甲状腺和肾上腺皮质功能正常。给予3天的人绒毛膜促性腺激素(HCG)后,血浆睾酮水平从0.15微克%升至0.45微克%。双侧性腺切除术后,血浆睾酮水平降至0.06微克%,给予HCG后无反应。回顾了1937年至1973年间世界文献报道的109例混合性性腺发育不全(MGD)病例和2例单侧性腺发育不全病例。根据其临床和病理特征,后两例患者被排除在MGD类别之外。在109例MGD病例中的15例中,一个掩盖起源性腺的性腺母细胞瘤与一个发育异常的性腺相对,后者有或没有性腺母细胞瘤,或者没有性腺。在这些病例中,组织学上未证实有睾丸存在,其临床病理特征与纯性腺发育不全相似。在其余94例MGD病例中,72例一侧有睾丸组织,另一侧为条索状或胚胎性腺,22例有睾丸但对侧无性腺……