ANDREW I. SCHAFER, M.D.; J. BRUCE MILLER, M.D.; ERIC P. LESTER, M.D.; TIMOTHY K. BOWERS, M.D.; HARRY S. JACOB, M.D.
Two cases of monoclonal gammopathy in patients with hereditary spherocytosis led us to consider the possbile pathogenetic relation between these two disorders. Twelve adult patients with hereditary spherocytosis had significant hypergammaglobulinemia in comparison to normal subjects. Retrospective analysis of previous illness in 140 patients with multiple myeloma showed a significant association between IgA myeloma and previous gallbladder disease. We propose that the chronic reticuloendothelial stimulation due to extravascular hemolysis, possibly potentiated by the inflammation associated with cholelithiasis and cholecystitis, may foster neoplastic transformation of immunocytes in patients with hereditary spherocytosis, ultimately leading to the development of monoclonal gammopathy.
SCHAFER AI, MILLER JB, LESTER EP, BOWERS TK, JACOB HS. Monoclonal Gammopathy in Hereditary Spherocytosis: A Possible Pathogenetic Relation. Ann Intern Med. 1978;88:45–46. doi: 10.7326/0003-4819-88-1-45
Download citation file:
Published: Ann Intern Med. 1978;88(1):45-46.
Hematology/Oncology, Red Cell Disorders.
Results provided by:
Copyright © 2019 American College of Physicians. All Rights Reserved.
Print ISSN: 0003-4819 | Online ISSN: 1539-3704
Conditions of Use