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[伴有肾上腺发育不全的神经垂体先天性缺陷]

[Congenital defects of neurohypophysis with adrenal hypoplasia].

作者信息

Babala J, Brozman M, Halamová V

出版信息

Zentralbl Allg Pathol. 1982;126(3-4):277-85.

PMID:7148183
Abstract

Congenital adrenal hypoplasia without expressive diencephalic malformation is rare. Autopsy findings in two newborn girls with hypoplasia of the neurohypophysis or aplasia of neurohypophysis combined with severe cortical adrenal hypoplasia, resp., are reported. The weight of both adrenals in the case with neurohypophyseal hypoplasia was 0,39 g, and in the case with aplasia of neurohypophysis it was 0,27 g. In both cases the adenohypophysis was poorly differentiated and the number of R and S cells was considerably reduced. In the case with aplasia of neurohypophysis, R cells were identified only by use of the immune fluorescence staining technique. Moderate hypoplasia and interstitial fibrosis were also found in thyroid gland and gonads. In both cases, the hypothalamic-pituitary connection, i.e., the infundibulum and pituitary portal system were missing and, consequently, the supply of secretion-stimulating hypothalamic substances to adenohypophysis via portal system was disturbed.

摘要

无表达性间脑畸形的先天性肾上腺发育不全很罕见。报告了两名新生女婴的尸检结果,分别为神经垂体发育不全或神经垂体缺如合并严重皮质肾上腺发育不全。神经垂体发育不全病例中双侧肾上腺重量为0.39克,神经垂体缺如病例中为0.27克。两例中腺垂体分化不良,R细胞和S细胞数量显著减少。在神经垂体缺如的病例中,仅通过免疫荧光染色技术鉴定出R细胞。甲状腺和性腺也发现中度发育不全和间质纤维化。两例中均未发现下丘脑 - 垂体连接,即漏斗和垂体门脉系统,因此,通过门脉系统向腺垂体供应下丘脑分泌刺激物质受到干扰。

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