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Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting
Published on: May 1, 2015
Recurrent hemolytic uremic syndrome associated with intestinal lymphangiectasia
Süleyman Kalman1, Sevcan Bakkaloğlu, Buket Dalgiç
1Department of Pediatric Nephrology, Gazi University, Besevler, Ankara, Turkey. suleymankalman@yahoo.com
Abstract:
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 enteropathy and hypocomplementemia due to intestinal lymphangiectasia is may be a rare cause of atypical HUS.
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