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Cancer Genet Cytogenet ; 74(1): 35-9, 1994 May.
Article in English | MEDLINE | ID: mdl-8194045

ABSTRACT

The chromosome der(1;7)(q10;p10) consists of the short arm of chromosome 7 and the long arm of chromosome 1, and is a common abnormality in treatment-related leukemia and myelodysplastic syndrome. Here we describe a 39-year-old Japanese man with acute myeloblastic leukemia (FAB-M2) exhibiting t(8;21)(q22;q22). He entered complete remission after induction therapy, and intensification therapy including alkylating agents was subsequently continued for 3 years. The patient then developed pancytopenia; bone marrow aspiration revealed myelodysplastic syndrome exhibiting the der (1;7) chromosome. To our knowledge, this is the first reported case of such an abnormality in myelodysplastic syndrome secondary to acute myeloblastic leukemia with the 8;21 translocation.


Subject(s)
Anemia, Refractory, with Excess of Blasts/genetics , Chromosomes, Human, Pair 1 , Chromosomes, Human, Pair 21 , Chromosomes, Human, Pair 7 , Chromosomes, Human, Pair 8 , Leukemia, Myeloid, Acute/genetics , Translocation, Genetic , Adult , Anemia, Refractory, with Excess of Blasts/chemically induced , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Humans , Karyotyping , Leukemia, Myeloid, Acute/drug therapy , Male
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