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尿道梗阻畸形综合征:腹肌发育不全及“梅干腹”的一个病因

Urethral obstruction malformation complex: a cause of abdominal muscle deficiency and the "prune belly".

作者信息

Pagon R A, Smith D W, Shepard T H

出版信息

J Pediatr. 1979 Jun;94(6):900-6. doi: 10.1016/s0022-3476(79)80210-3.

Abstract

Abdominal muscle deficiency with a "prune belly" abdomen as been a major feature of the so-called prune belly syndrome, which has been regarded as a specific entity, although the etiology and developmental pathology are not understood. We present evidence that abdominal muscle deficiency is an etiologically nonspecific anatomic defect which is secondary to fetal abdominal distention of various causes. One of the more common causes is urethral obstruction with consequent early bladder distention, causing abdominal distention and other anomalies, a constellation of findings which we have termed the urethral obstruction malformation complex. This interpretation of the etiology of most cases of prune belly syndrome accounts for the male predominance, the observed variability in severity, and the lack of a defined mode of inheritance. Recurrence risk figures need to be redefined for each specific obstructing lesion of the urethra. The possibility of early prenatal diagnosis and management of fetuses with urethral obstruction needs further study.

摘要

腹部肌肉发育不全伴“梅干腹”一直是所谓梅干腹综合征的主要特征,尽管其病因和发育病理学尚不清楚,但该综合征一直被视为一种特定的疾病实体。我们提供的证据表明,腹部肌肉发育不全是一种病因非特异性的解剖学缺陷,是由各种原因导致的胎儿腹部膨胀继发而来。较常见的原因之一是尿道梗阻,继而早期膀胱膨胀,导致腹部膨胀及其他异常,这一系列表现我们称之为尿道梗阻畸形复合体。对大多数梅干腹综合征病例病因的这种解释说明了男性发病率高、观察到的严重程度差异以及缺乏明确的遗传方式。需要针对尿道的每种特定梗阻性病变重新定义复发风险数字。对尿道梗阻胎儿进行早期产前诊断和处理的可能性需要进一步研究。

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