> top > docs > PubMed:10435360 > annotations

PubMed:10435360 JSONTXT

Annnotations TAB JSON ListView MergeView

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 152-160 HP_0001909 denotes leukemia
T2 161-169 HP_0002665 denotes lymphoma

DisGeNET

Id Subject Object Predicate Lexical cue
T0 0-4 gene:4684 denotes CD56
T1 10-37 disease:C3150773 denotes stem cell leukemia/lymphoma
R1 T0 T1 associated_with CD56,stem cell leukemia/lymphoma

PubMed_Structured_Abstracts

Id Subject Object Predicate Lexical cue
T1 77-170 OBJECTIVE denotes We describe the characteristics of three patients with CD56+CD7+ stem cell leukemia/lymphoma.
T2 180-342 METHODS denotes These blasts were analyzed for morphologic, karyotypic, immunophenotypic, and immunogenotypic features using Southern blot and polymerase chain reaction analysis.
T3 354-509 METHODS denotes Peripheral blood, bone marrow aspirates, or biopsied mediastinal tumor specimens of three CD56+CD7+ stem cell leukemia/lymphoma patients were investigated.
T4 519-1661 RESULTS denotes The bone marrow of all patients showed myeloperoxidase (MPO) negative blast cells with basophilic cytoplasm and distinct nucleoli with no azurophilic granules. The blasts of two patients were classified as acute lymphoblastic leukemia (L2). The liver, spleen, and lymph nodes were unaffected in all patients. All had an aggressive clinical course. The blasts were strongly positive for both CD7 and CD56 but negative for other T-lineage associated antigens, including CD1, CD2, surface membrane CD3, cytoplasmic CD3c (2/2), CD4, CD5 and CD8. The additional antigens were recognized as follows: CD19 (1/3 cases) as a B lineage, CD33 (1/3) as a myeloid marker, CD34 (2/3) as a stem cell, CD38 (1/1) and HLA-DR (2/3). When the patients relapsed, the phenotypes changed to blasts positive for CD5, CD10 and CD13 in patient 1, CD5 in patient 2, and CD33 in patient 3. MPO, however, remained negative. Cytogenetic analysis showed no common abnormal karyotype. All had a common D2-Jdelta1 induced by T-cell specific enhancer. Rearrangement of TCR beta and gamma genes occurred in patient 2, and IgH and TCR beta underwent rearrangement in patient 3.
T5 1674-1917 CONCLUSIONS denotes Although a more comprehensive case analysis is necessary, these data suggest the possibility that the blasts of the present cases come from a common lymphoid precursor (T, NK, and B cell) or from a NKT precursor as the fourth lymphoid lineage.