2017
DOI: 10.1200/po.17.00186
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Not So Typical: Development of Atypical Chronic Myeloid Leukemia in a Patient With Chronic Myeloid Leukemia

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Cited by 3 publications
(3 citation statements)
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“…Chronic myeloid leukemia (CML) is a hematologic clonal malignancy that is produced by hematopoietic stem cells (HSC). [ 52 ] CML, a distinctive cytogenetic abnormality, involves the translocation of the Abelson oncogene 1 (ABL1) on chromosome 9, and breakpoint cluster region (BCR) on chromosome 22, t(9;22)(q34;q11.2), ensuing BCR-ABL gene union well-known Philadelphia positive (Ph+) chromosome [ 53 ]…”
Section: Chronic Myeloid Leukemiamentioning
confidence: 99%
See 1 more Smart Citation
“…Chronic myeloid leukemia (CML) is a hematologic clonal malignancy that is produced by hematopoietic stem cells (HSC). [ 52 ] CML, a distinctive cytogenetic abnormality, involves the translocation of the Abelson oncogene 1 (ABL1) on chromosome 9, and breakpoint cluster region (BCR) on chromosome 22, t(9;22)(q34;q11.2), ensuing BCR-ABL gene union well-known Philadelphia positive (Ph+) chromosome [ 53 ]…”
Section: Chronic Myeloid Leukemiamentioning
confidence: 99%
“…Chronic Myeloid Leukemia Chronic myeloid leukemia (CML) is a hematologic clonal malignancy that is produced by hematopoietic stem cells (HSC). [52] CML, a distinctive cytogenetic abnormality, involves the translocation of the Abelson oncogene 1 (ABL1) on chromosome 9, and breakpoint cluster region (BCR) on chromosome 22, t(9;22)(q34;q11.2), ensuing BCR-ABL gene union well-known Philadelphia positive (Ph+) chromosome [53] Between 90% and 96%, Philadelphia positive (Ph+) chromosomes in CML were detected. By altering the (3' to 5') segment of the ABL oncogene (9q34) and BCR gene (22q11.2), respectively, the BCR-ABL fusion gene, which encodes a constitutive TK active oncoprotein.…”
Section: Sars-cov-2: Preventionmentioning
confidence: 99%
“…4,7,11,12 Increased total leukocyte count (>50 × 10 9 /l), increased percentage of immature white blood cells, hemoglobin level <10gm/dl, age > 65 years, and presence of three or more chromosome mutations have been linked to decreased morbidity and mortality. 2,13,14 In 20 to 40% cases of aCML, they evolve to acute myeloid leukaemia (AML) within 18 months of diagnosis. 4,15 Certain predisposing factors such as enlarged liver or spleen, elevated levels of monocytes (>3 × 10 9 /l but <8 × 10 9 /l), >5% of blasts in the bone marrow have been linked to the increased chances of progression to AML.…”
Section: Introductionmentioning
confidence: 99%