Open AccessRed Cell Hypoplasia, Cold Hemoglobinuria and M-Type Gamma G Serum Paraprotein and Bence Jones Proteinuria in a Patient With Lymphoproliferative Disorder
Author(s) -
Ananda S. Prasad,
Lawrence Berman,
Liborio Tranchida,
M. D. Poulik
Publication year - 1968
Publication title -
blood
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.515
H-Index - 465
eISSN - 1528-0020
pISSN - 0006-4971
DOI - 10.1182/blood.v31.2.151.151
Subject(s) - hypogammaglobulinemia , bence jones protein , medicine , proteinuria , multiple myeloma , macroglobulinemia , paroxysmal nocturnal hemoglobinuria , waldenstrom macroglobulinemia , paraproteins , lymphoproliferative disorders , paraproteinemia , pathology , immunology , monoclonal , antibody , lymphoma , immunoglobulin light chain , monoclonal antibody , kidney
This paper documents an unusual example of hypoplastic anemia, intermittent hemoglobinuria appearing in cold weather, and lymphoproliferative disease associated with hypogammaglobulinemia and repeated infections, followed by the appearance of a monoclonal gammopathy (IgG-Kappa) and Bence Jones proteinuria (Kappa), with tissue lesions more characteristic of macroglobulinemia than of multiple myeloma, in a middle-aged Negro.
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