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真两性畸形是原发性生殖细胞疾病吗?

Is true hermaphroditism a primary germ cell disorder?

作者信息

McKelvie P, Jaubert F, Nezelof C

出版信息

Pediatr Pathol. 1987;7(1):31-41. doi: 10.1080/15513818709177112.

Abstract

Eleven cases of true hermaphroditism, 6 raised as female and 5 as male, were seen in the 20-year period from 1965 to 1985. External genitalia varied from Prader types II to IV. The ovotestis (11/22) was the most common gonad, and a marked variation in macroscopic and microscopic appearances with five patterns of distribution of gonadal tissue was noted. Ovulation was observed in ovarian tissue, and spermatogonia, but no spermatozoa, in testicular tubules. A hypothesis is developed suggesting abnormal testicular differentiation, and a model is presented to explain observed patterns of gonadal tissue distribution. A uterus was present in all cases, but a hemiuterus or lateralized uterus was noted in the 5 cases in which only testicular or predominantly testicular tissue was observed on the contralateral side. Karyotype analysis showed 46 XX in 5 cases (1 with an H-Y antigen) and a mosaic involving 46 XY in the remaining 5. Spontaneous puberty was achieved in 3 of the females, and of the 4 males with residual testicular tissue, all are prepubertal.

摘要

在1965年至1985年的20年期间,共发现11例真两性畸形病例,其中6例按女性抚养,5例按男性抚养。外生殖器从普拉德II型到IV型不等。卵睾(11/22)是最常见的性腺,性腺组织的宏观和微观表现存在明显差异,观察到性腺组织分布有五种模式。在卵巢组织中观察到排卵,在睾丸小管中观察到精原细胞,但未观察到精子。提出了一个假说,认为睾丸分化异常,并给出了一个模型来解释观察到的性腺组织分布模式。所有病例均有子宫,但在5例对侧仅观察到睾丸或主要为睾丸组织的病例中,发现有半子宫或偏侧子宫。染色体核型分析显示,5例为46 XX(1例有H-Y抗原),其余5例为涉及46 XY的嵌合体。3名女性实现了自然青春期,4名有残余睾丸组织的男性均处于青春期前。

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