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Int J Hematol ; 77(5): 518-21, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12841392

ABSTRACT

Therapy-related myelodysplastic syndrome and therapy-related acute myelocytic leukemia (AML) are now recognized as hematologic malignancies that occur a few years after chemotherapy for primary malignancy with alkylating agents or topoisomerase II inhibitors. The secondary leukemia is usually AML and sometimes is preceded by a myelodysplastic syndrome. Acute lymphoblastic leukemia (ALL) as a secondary leukemia is quite rare, and secondary T-cell ALL after AML is even rarer. We report a case of a 56-year-old woman who developed T-cell ALL after a 3-year remission of AML (M2). We thought that this case would be extremely valuable for studying the etiology and biological characteristics of T-cell ALL as a secondary leukemia after AML.


Subject(s)
Leukemia, Myeloid, Acute/pathology , Leukemia, T-Cell/etiology , Neoplasms, Second Primary/etiology , Precursor Cell Lymphoblastic Leukemia-Lymphoma/etiology , Chromosomes, Human, Pair 14 , Chromosomes, Human, Pair 6 , Female , Gene Rearrangement , Genes, T-Cell Receptor , Humans , Leukemia, Myeloid, Acute/drug therapy , Leukemia, T-Cell/diagnosis , Leukemia, T-Cell/genetics , Middle Aged , Neoplasms, Second Primary/diagnosis , Neoplasms, Second Primary/genetics , Precursor Cell Lymphoblastic Leukemia-Lymphoma/diagnosis , Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics , Remission Induction , Translocation, Genetic
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