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Rev. méd. Chile ; 122(9): 1052-5, sept. 1994. ilus
Article in Spanish | LILACS | ID: lil-138050

ABSTRACT

We present the clinical and laboratory features of 2 patients with B prolymphocitic leukemia. Both are females of the fith and seventh decade of life. One had the classical clinical picture of massive splenomegaly and a high white cell count, with characteristic prolymphocytes and the other was asymptomatic, with a low white cell count. The cells were positive to B cell lineage reagents with strong surface immunoglobuline (Ig) and unreactive to T cell antibodies. Analysis of Ig genes at the DNA level demonstrated that both cases had heavy-chain gene rearrangements, confirming the B-cell origin. These are the first patients of prolymphocytic leukemia described in Chile


Subject(s)
Middle Aged , Leukemia, Prolymphocytic/diagnosis , DNA Probes/analysis , Immunophenotyping/methods , Genetic Markers/immunology
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