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
收藏
页码：246 / 249
页数：4
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