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巨膀胱-小结肠-肠蠕动减少综合征:新生儿肠梗阻的一个新病因。5例新生儿女孩的放射学表现报告。

Megacystis-microcolon-intestinal hypoperistalsis syndrome: a new cause of intestinal obstruction in the newborn. Report of radiologic findings in five newborn girls.

作者信息

Berdon W E, Baker D H, Blanc W A, Gay B, Santulli T V, Donovan C

出版信息

AJR Am J Roentgenol. 1976 May;126(5):957-64. doi: 10.2214/ajr.126.5.957.

DOI:10.2214/ajr.126.5.957
PMID:178239
Abstract

Five newborn girls presented with small intestinal obstruction and microcolon and a giant bladder (megacystis). Organic causes of obstruction were not found, and the gastrointestinal tract failed to function after appropriate diversion. Two died in the postoperative period, two lived several months on central venous hyperalimentation, and one died at 34 months of age following chronic though intermittent hyperalimentation. Pathologic studies showed an abundance of ganglion cells in both dilated and narrowed areas of intestine; the combined small bowel-colon length was one-third of normal in the absence of an evident obstructive or vascular insult. The five patients represent the most severe manifestation of defective intestinal peristalsis in a larger group of distended newborns in whom organic gastrointestinal obstruction is not found. Treatment with central venous hyperalimentation may sustain life, and some patients eventually recover gastrointestinal function. The hypoperistalsis is largely refractory to pharmacologic treatment; its cause is unknown.

摘要

五名新生女婴出现小肠梗阻、小结肠和巨大膀胱(巨膀胱)。未发现梗阻的器质性病因,经适当转流后胃肠道仍无法正常运作。两名患儿术后死亡,两名患儿通过中心静脉高营养维持了数月生命,一名患儿在接受长期但间歇性高营养治疗后于34个月龄死亡。病理研究显示,在肠道扩张和狭窄区域均有大量神经节细胞;在没有明显梗阻或血管损伤的情况下,小肠和结肠的总长度仅为正常的三分之一。这五名患者代表了一大组腹胀新生儿中肠道蠕动缺陷的最严重表现,这些新生儿未发现器质性胃肠道梗阻。中心静脉高营养治疗可维持生命,一些患者最终恢复胃肠道功能。这种蠕动减弱在很大程度上对药物治疗无效;其病因不明。

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