| Literature DB >> 26155548 |
Bhoumik Shah1, Smeeta Gajendra2, Ritu Gupta3, Atul Sharma4.
Abstract
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.Entities:
Keywords: Complex cytogenetics; Monosomy 13; t(15;20)(q22;p13); t(5;13)(q12;p13)
Year: 2015 PMID: 26155548 PMCID: PMC4484140 DOI: 10.7860/JCDR/2015/12284.5940
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X