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梅干腹综合征与女性假两性畸形

Prune belly syndrome and female pseudohermaphroditism.

作者信息

Grosse Hokamp H, Müller K M

出版信息

Pathol Res Pract. 1983 Jun;177(1):77-83. doi: 10.1016/S0344-0338(83)80045-4.

Abstract

The "prune belly" syndrome (PBS) combines malformation of the deferent urinary tract with cryptorchism and hypoplasia or aplasia of the abdominal musculature. Recent investigations have ascertained the role of urethral atresia or temporary urethral stenosis in the pathogenesis of PBS. The present case is classified as PBS combined with female pseudohermaphroditism and urethral atresia in a Potter syndrome. Of paradigmatic significance for the understanding of PBS pathogenesis, the case illustrates the almost exclusive occurrence of the syndrome in males, explained by the complex evolution of the phallic urethra. Hypoplasia of abdominal muscles is seen as a sequel to the extreme occupation of intraabdominal space. An alternative concept, assuming general defects in mesenchymal development that provoke independent, isolated malformations eventually subsumed under the term prune belly syndrome, is discussed in this context.

摘要

“梅干腹”综合征(PBS)合并了输精管泌尿系统畸形、隐睾症以及腹部肌肉发育不全或发育不全。最近的研究已经确定尿道闭锁或暂时性尿道狭窄在PBS发病机制中的作用。本病例被归类为PBS合并波特综合征中的女性假两性畸形和尿道闭锁。该病例对于理解PBS发病机制具有范式意义,它说明了该综合征几乎仅发生于男性,这可以通过阴茎尿道的复杂发育来解释。腹部肌肉发育不全被视为腹腔内空间极度占据的后遗症。在此背景下,还讨论了另一种概念,即假设间充质发育存在普遍缺陷,从而引发最终被归入梅干腹综合征这一术语下的独立、孤立畸形。

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