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Korean Journal of Pediatrics ; : 224-227, 2005.
Article in Korean | WPRIM | ID: wpr-12605

ABSTRACT

Henoch-Schonlein purpura(HSP) is an IgA mediated immune complex vasculitic disease characterized by non-thrombocytic purpura, arthritis, gastrointestinal manifestations, and glomerulonephritis. HSP related glomerulonephritis induces hypoproteinemia and edema in some cases. Protein-losing enteropathy is another rare but known manifestation of HSP leading to hypoproteinemia and edema. We report a 6-year-old girl with HSP who showed edema caused by intestinal protein loss, evidenced by elevated fecal alpha 1 antitrypsin clearance.


Subject(s)
Child , Female , Humans , alpha 1-Antitrypsin , Antigen-Antibody Complex , Arthritis , Edema , Glomerulonephritis , Hypoproteinemia , Immunoglobulin A , Protein-Losing Enteropathies , Purpura , IgA Vasculitis
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