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Korean Journal of Pediatrics ; : 224-227, 2005.
Artigo em Coreano | WPRIM | ID: wpr-12605

RESUMO

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.


Assuntos
Criança , Feminino , Humanos , alfa 1-Antitripsina , Complexo Antígeno-Anticorpo , Artrite , Edema , Glomerulonefrite , Hipoproteinemia , Imunoglobulina A , Enteropatias Perdedoras de Proteínas , Púrpura , Vasculite por IgA
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