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先天性钠腹泻,空肠刷状缘膜钠转运存在部分缺陷,直肠转运正常,腹泻可缓解。

Congenital sodium diarrhea with a partial defect in jejunal brush border membrane sodium transport, normal rectal transport, and resolving diarrhea.

作者信息

Fell J M, Miller M P, Finkel Y, Booth I W

机构信息

Institute of Child Health, University of Birmingham, England.

出版信息

J Pediatr Gastroenterol Nutr. 1992 Aug;15(2):112-6. doi: 10.1097/00005176-199208000-00002.

Abstract

Defective jejunal sodium/proton exchange causes severe, congenital secretory diarrhea. We report a boy who presented typically in utero, but in whom diarrhea resolved during the first year of life. Pregnancy was complicated by polyhydramnios, and an ultrasound at 31 weeks showed a distended fetal small intestine. The abdomen was grossly distended at birth, and profuse secretory diarrhea began immediately. He subsequently thrived on breast milk and electrolyte supplements. Studies of jejunal brush border sodium/proton exchange at 6 months showed a partial defect. Nonequilibrium rectal dialysis showed rectal sodium and potassium transport to be intact. Diarrhea lessened after 9 months, and the patient subsequently required occasional laxatives. These observations suggest that there is a spectrum of congenital abnormality in this exchanger, and that in children with incomplete defects normal colonic sodium salvage can subsequently mask net small intestinal secretion.

摘要

空肠钠/质子交换缺陷会导致严重的先天性分泌性腹泻。我们报告了一名典型的在子宫内就出现症状的男孩,但他的腹泻在出生后的第一年就得到了缓解。妊娠合并羊水过多,孕31周时超声检查显示胎儿小肠扩张。出生时腹部明显膨隆,随即开始出现大量分泌性腹泻。随后,他依靠母乳和电解质补充剂茁壮成长。6个月时对空肠刷状缘钠/质子交换的研究显示存在部分缺陷。非平衡直肠透析显示直肠钠和钾转运功能正常。9个月后腹泻减轻,患者随后偶尔需要使用泻药。这些观察结果表明,这种交换器存在一系列先天性异常,并且在存在不完全缺陷的儿童中,正常的结肠钠重吸收随后可能掩盖小肠的净分泌。

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