MULTIPLE-MYELOMA ARISING FROM MONOCLONAL GAMMOPATHY OF UNDETERMINED SIGNIFICANCE IN A PATIENT WITH GAUCHERS-DISEASE

Citation
K. Brady et al., MULTIPLE-MYELOMA ARISING FROM MONOCLONAL GAMMOPATHY OF UNDETERMINED SIGNIFICANCE IN A PATIENT WITH GAUCHERS-DISEASE, Archives of pathology and laboratory medicine, 121(10), 1997, pp. 1108-1111
Citations number
15
Categorie Soggetti
Pathology,"Medical Laboratory Technology","Medicine, Research & Experimental
Journal title
Archives of pathology and laboratory medicine
ISSN journal
00039985 → ACNP
Volume
121
Issue
10
Year of publication
1997
Pages
1108 - 1111
Database
ISI
SICI code
0003-9985(1997)121:10<1108:MAFMGO>2.0.ZU;2-B
Abstract
We report the case of a 64-year-old woman who, 12 years after receivin g a diagnosis of Gaucher's disease with concurrent monoclonal gammopat hy of undetermined significance, developed worsening thrombocytopenia and bone pain. Bone marrow biopsy at this time revealed 50% plasma cel ls with a serum monoclonal immunoglobulin A-lambda level of 3.2 g/L. R oentgenography revealed a lytic clavicular lesion, and a diagnosis of multiple myeloma was made. To our knowledge, this case is the first to document the evolution of a monoclonal gammopathy of undetermined sig nificance to multiple myeloma in a patient with Gaucher's disease. The importance of investigating cytopenias and increased bone pain in suc h patients, perhaps by bone marrow biopsy, to rule out potentially mal ignant plasma cell dyscrasias is stressed.