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A child with Philadelphia positive (Ph+)-acute leukemia with myeloid morphology: one case of stem cell origin.

Authors :
Hassan R
Otazú I
Ornellas MH
Pires V
Carriço MK
Seuánez H
Tabak D
Zalcberg I
Source :
Leukemia & lymphoma [Leuk Lymphoma] 2004 Sep; Vol. 45 (9), pp. 1925-9.
Publication Year :
2004

Abstract

Philadelphia positive (Ph+) acute myeloid leukemia (AML) is a rare and heterogeneous condition, mainly reported in adults, associated to poor prognosis and unfavorable response to therapy. Here we report clinical and laboratory findings in an 8-year-old patient diagnosed with Ph+ acute leukemia with myeloid (FAB M4) morphology. The patient consistently expressed variable levels of m-bcr, e1a2 transcripts during a 42-month follow-up after two different stem cell transplantation protocols. An immunophenotypic switch was documented, from a mixed, myeloid-lymphoid lineage to a full lymphoid phenotype following stem cell transplants, in association with an immature B-cell gene rearrangement profile and clonal instability during clinical progression. This report indicates a stem cell origin as previously suggested for Ph+ AML.<br /> (Copyright 2004 Taylor and Francis Ltd)

Details

Language :
English
ISSN :
1042-8194
Volume :
45
Issue :
9
Database :
MEDLINE
Journal :
Leukemia & lymphoma
Publication Type :
Academic Journal
Accession number :
15223656
Full Text :
https://doi.org/10.1080/10428190410001663662