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Acute Myeloid Leukemia With T-Lymphoid Features: A Distinct Biologic and Clinical Entity
Blood, 1988-08, Vol.72 (2), p.579-587
Cross, Anne H.
Goorha, Rakesh M.
Nuss, Rachelle
Behm, Frederick G.
Murphy, Sharon B.
Kalwinsky, David K.
Raimondi, Susana
Kitchingman, Geoffrey R.
Mirro, Joseph
1988
Details
Autor(en) / Beteiligte
Cross, Anne H.
Goorha, Rakesh M.
Nuss, Rachelle
Behm, Frederick G.
Murphy, Sharon B.
Kalwinsky, David K.
Raimondi, Susana
Kitchingman, Geoffrey R.
Mirro, Joseph
Titel
Acute Myeloid Leukemia With T-Lymphoid Features: A Distinct Biologic and Clinical Entity
Ist Teil von
Blood, 1988-08, Vol.72 (2), p.579-587
Ort / Verlag
Washington, DC: Elsevier Inc
Erscheinungsjahr
1988
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
We studied the clinical and biologic features of 10 cases of acute leukemia that met standard French-American-British (FAB) criteria for acute myeloid leukemia (AML) but in which the blast cells also expressed the T-cell-associated CD2 surface antigen. All cases had >3% myeloperoxidase and Sudan black B-positive leukemic blasts, and blasts from seven cases contained Auer rods. Reactivity of the cells with a panel of monoclonal antibodies (MAbs) indicated that leukemic cells in all cases expressed myeloid- associated (CD11b, CD13) surface antigens, further supporting the diagnosis of AML. However, blasts from every patient coexpressed the T-cell-associated surface CD2 and CD7 as well as cytoplasmic CD3 antigens. Blasts from five patients expressed surface CD25, whereas blasts from only one expressed surface CD3. Five patients had rearranged T-cell receptor β -chain genes, whereas only three had rearranged T-cell receptor γ-chain genes. This pattern of lineage-related gene expression appears to define a distinct subtype of AML with T-lymphoid features (CD2+ AML) and could reflect either aberrant gene expression in leukemic blasts or transformation of a pluripotent stem cell having a flexible pattern of gene expression. Clinically, these 10 patients presented at an older age with a higher leukocyte count and a higher frequency of lymphadenopathy than did children whose blast cells were characteristic of myeloid leukemia. Patients with CD2+ AML also had poorer responses to remission induction therapy (50% v 80% entered complete remission, P = .05). However, each of the five children who failed induction chemotherapy on AML protocols had a striking response to drug combinations usually reserved for lymphoid leukemia. We conclude that this leukemia with mixed lymphoid and myeloid characteristics is a distinct biologic and clinical entity. © 1988 by Grune & Stratton, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 0006-4971
eISSN: 1528-0020
DOI: 10.1182/blood.V72.2.579.579
Titel-ID: cdi_proquest_miscellaneous_78347534
Format
–
Schlagworte
Adolescent
,
Adult
,
Antigens, Surface - analysis
,
Biological and medical sciences
,
Bone Marrow - pathology
,
Child
,
Female
,
Hematologic and hematopoietic diseases
,
Humans
,
Karyotyping
,
Leukemia, Myeloid, Acute - drug therapy
,
Leukemia, Myeloid, Acute - immunology
,
Leukemia, Myeloid, Acute - pathology
,
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
,
Male
,
Medical sciences
,
Phenotype
,
Receptors, Antigen, T-Cell - genetics
,
Recombination, Genetic
,
T-Lymphocytes - immunology
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