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Classifying acute leukemia by immunophenotyping: a combined FAB-
immunologic classification of AML
PB Neame, P Soamboonsrup, GP Browman, RM Meyer, A Benger, WE Wilson, IR Walker, N Saeed and JA McBride
A panel of commercially available monoclonal antibodies and five
heteroantisera were used to distinguish and subtype 138 cases of acute
leukemia (AL). The immunophenotype was compared with the French-
American-British (FAB) classification obtained on the cases. The
immunophenotype discriminated acute myelogenous leukemia (AML) from acute
lymphoblastic leukemia (ALL) and recognized cases not distinguished by
cytochemistry (22% of cases), mixed lineage phenotypes (13% of cases), and
cases with separate populations of lymphoblasts and myeloblasts (one case).
Using the immunologic panel and derived criteria to subtype AML,
correspondence of the immunophenotype to the FAB subtypes M1, M2, M4, and
M5 was possible in greater than 80% of cases. A combined classification of
the immunophenotype and FAB morphology/cytochemistry was devised for AML
subtyping. It is recommended that immunophenotyping should be done at least
in all cases with negative or inconclusive cytochemistry. At present, we
suggest that until a "gold standard" for identifying leukemic subtypes is
developed, the best method for typing acute leukemia is by using a
combination of morphology, cytochemistry and immunophenotyping.
Volume 68,
Issue 6,
pp. 1355-1362,
12/01/1986
Copyright © 1986 by The American Society of Hematology

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