Abstract
A patient with CML is presented in whom Gaucher’s cells were seen in the bone marrow and other tissues. Biochemical and electron microscopic studies established the similarity of these cells to those found in Gaucher’s disease. Evidence is presented which indicates that the granulocyte is normally the major source of sphingolipid and that the Gaucher’s cells seen in CML arise from excessive granulocyte turnover.
This content is only available as a PDF.
© 1969 by American Society of Hematology, Inc.
1969
This feature is available to Subscribers Only
Sign In or Create an Account Close Modal