| Literature DB >> 8080883 |
M Van de Casteele1, G E Verhoef, H Demuynck, P Zacheé, M A Boogaerts.
Abstract
We describe a patient with a long history of typical chronic lymphocytic leukemia (CLL) who developed hypercalcemia, osteolytic bone lesions, and a monoclonal protein, all features of a secretory plasma cell disorder. These features in CLL have been reported in only four previous cases. The hypercalcemia in our patient is felt to result from an increase in the osteoclastic process.Entities:
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Year: 1994 PMID： 8080883 DOI： 10.1007/bf01698486
Source DB: PubMed Journal: Ann Hematol ISSN： 0939-5555 Impact factor: 3.673