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[A case of light chain deposition disease involving kidney and bone marrow with microangiopathic hemolytic anemia.] The Korean journal of laboratory medicine [Korean J Lab Med] Journal article

 
Title[A case of light chain deposition disease involving kidney and bone marrow with microangiopathic hemolytic anemia.]
Author(s)Cho YU, Chi HS, Park CJ, Jang S, Cho YM, Park JS 
InstitutionDepartment of Laboratory Medicine, Eulji University School of Medicine, Eulji General Hospital, Seoul, Kerea.
SourceKorean J Lab Med 2009 Oct; 29(5):384-9.
AbstractWe report a case of light chain deposition disease in a 59-yr-old female showing deposition of monoclonal light chain in the kidney and bone marrow accompanied with a schistocytosis, the morphologic finding of microangiopathic hemolytic anemia. The immunofluorescence examination of the kidney revealed strongly stained kappa-light chain deposits on the glomerular mesangium and capillary wall, tubules, and vessel wall. The electron microscopy demonstrated electron-dense deposits on the glomerular basement membrane and mesangium. Anemia was observed with schistocytosis and Howell-Jolly body in the peripheral blood smears. The immunohistochemical examination of the bone marrow showed the presence of kappa-light chain deposits in scattered plasma cells and thickened vessel wall in the absence of a prominent plasma cell proliferation. Although an immunofixation electrophoresis failed to detect a monoclonal gammopathy, the presence of monoclonal protein could be identified by an abnormal kappa/lambda ratio on the serum free light chain analysis.
Languagekor
Pub Type(s)English Abstract
Journal Article
PubMed ID19893345