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Leukemia ; 10(12): 1990-2, 1996 Dec.
Article in English | MEDLINE | ID: mdl-8946942

ABSTRACT

We report the clinical, hematological and immunophenotypic characteristics from four cases of acute leukemia with interstitial deletion of chromosome 9, ie del(9)(q12-q22), as a single chromosomal abnormality. Three patients had acute myeloblastic leukemia (AML) and one T origin acute lymphoblastic leukemia (ALL). According to FAB classification, blasts were classified as M1 (two patients), M2 (one patient), and L2 (one patient). In two out of three AML cases a myelodysplastic syndrome, one AREB-t and one AREB diagnosed 6 and 11 months before respectively, preceded the onset of AML. Morphological examination showed dysgranulopoiesis, dyserythropoiesis and cytoplasmic vacuoles in two AML patients, while a strong positivity to myeloperoxidases was observed in all AML cases. As concerns immunophenotypic findings, blast cells from two of three AML patients expressed CD7 and CD34, while those from the T-ALL case displayed CD33 and CD34 along with CD7. These observations suggest that del (9q) is associated with CD7+ acute leukemia of myeloid or lymphoid lineage.


Subject(s)
Antigens, CD7/analysis , Chromosome Deletion , Chromosomes, Human, Pair 9 , Leukemia, Myeloid, Acute/genetics , T-Lymphocytes/ultrastructure , Adolescent , Adult , Aged , Child , Female , Humans , Immunophenotyping , Male
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