Recurrent hemolytic uremic syndrome associated with intestinal lymphangiectasia

被引：1

作者：

Kalman, Sueleyman ^{[1
]}

Bakkaloglu, Sevcan

Dalgic, Buket

Oezkaya, Ozan

Soeylemezoglu, Oguz

Buyan, Necla

机构：

[1] Gazi Univ, Gulhane Mil Med Fac, Dept Pediat Nephrol, TR-06018 Ankara, Turkey

[2] Gazi Univ, Gulhane Mil Med Fac, Dept Pediat Gastroenterol, TR-06018 Ankara, Turkey

来源：

JOURNAL OF NEPHROLOGY | 2007年 / 20卷 / 02期

关键词：

hemolytic uremic syndrome; intestinal lymphangiectasia; hypocomplementemia;

D O I：

暂无

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

A 17-year-old boy was admitted to the hospital twice in a year for 2 episodes of hemolytic uremic syndrome (HUS). During these 2 HUS episodes he had diarrhea, decreased serum complement, decreased total protein and decreased serum albumin concentrations. We suggest that protein-losing enteropy and hypocomplementemia due to intestinal lymphangiectasia is may be rare cause of atypical HUS.

引用

页码：246 / 249

页数：4

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