全身平滑肌肥大。

Revista paulista de medicina Pub Date : 1992-07-01
A L da Silva, A Petroianu
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引用次数: 0

摘要

本报告报告一位二十岁男性,患有广泛性消化和泌尿平滑肌肥大,并伴有躯体和性发育不全。我们在文献中找不到任何与患者疾病相关的报道。先天性幽门狭窄是由于平滑肌肥大引起的较少见的梗阻性综合征。Morgagni在18世纪描述了一名成年患者的这种综合征(2)。幽门成形术是治疗这种疾病的最佳方法。其他先天性或获得性消化系统梗阻性综合征,如恰加斯神经节病和假性小肠梗阻,也是重要的临床和手术挑战(1,3,4)。一些由于平滑肌功能障碍引起的阻塞性疾病已经被描述过。本文报告了平滑肌肥厚引起的泌尿段梗阻。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Generalized smooth muscle hypertrophy.

This report presents a twenty-year-old man with generalized digestive and urinary smooth muscle hypertrophy combined with somatic and sexual hypodevelopment. We could not find in the literature any report related to the disease of our patient. Congenital pyloric stenosis is the less rare obstructive syndrome due to smooth muscle hypertrophy. Morgagni described this syndrome in an adult patient, in the XVIII century (2). Pyloroplasty is the best treatment for this disease. Other congenital or acquired obstructive syndromes of the digestive system such as Chagas' aganglionosis and pseudo-obstruction of the small bowel are also important clinical and surgical challenges (1,3,4). Several obstructive illnesses due to smooth muscle dysfunction have been described. This report presents an apparently original syndrome urinary segmental obstruction following smooth muscle hypertrophy.

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