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Novel Cytogenetic Aberrations in a Patient of Chronic Myeloid Leukemia with Blast Crisis
Author(s) -
B. S. Shah,
Smeeta Gajendra,
Ritu Gupta,
Atul Sharma
Publication year - 2015
Publication title -
journal of clinical and diagnostic research
Language(s) - English
Resource type - Journals
eISSN - 2249-782X
pISSN - 0973-709X
DOI - 10.7860/jcdr/2015/12284.5940
Subject(s) - chromosomal translocation , myeloid leukemia , karyotype , cytogenetics , acute promyelocytic leukemia , monosomy , bone marrow , imatinib , medicine , somatic evolution in cancer , pathology , chromosome , cancer research , biology , genetics , cancer , retinoic acid , gene
Chronic myeloid leukaemia (CML) is a clonal haematological disease which is characterized by a diagnostic karyotypic abnormality t (9;22)(q34;q11) called as Philadelphia (Ph) chromosome. Occurrence of additional chromosomal abnormalities besides the Ph chromosome is defined as clonal evolution (CE) and considered to be a marker of disease progression. A 67-year-old male who was initially evaluated at a private hospital where a diagnosis of acute promyelocytic leukaemia was made on bone marrow aspirate with ambiguous RT-PCR report referred to our centre for further evaluation and treatment. On conventional karyotyping, Ph chromosome along with translocations t(5;13)(q12;p13), t(15;20)(q22;p13) and monosomy 13 was observed in all 20 metaphases. A final diagnosis of CML-myeloid blast crisis with complex cytogenetics was made. Patient succumbed to death within one month of initiation of imatinib therapy.

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