Chronic myelogenous leukemia, BCR-ABL1 positive

Author:  Elizabeth L. Courville, MD, 01/20/2016
Category: Myeloid Neoplasms and acute leukemia (WHO 2016) > Myeloproliferative Neoplasms (MPN) > Chronic Myelogenous Leukemia (CML), BCR-ABL1+
Published Date: 01/21/2016
Chronic myelogenous leukemia (CML) is an uncommon disease which usually presents in middle-age but can occur at any age.

Many patients (20-40%) are asymptomatic at diagnosis of CML and are diagnosed on routine blood evaluation. Presenting symptoms can include splenomegaly and anemia.

Most patients are diagnosed in the chronic phase of CML.
Peripheral blood The peripheral blood shows a leukocytosis and includes neutrophils at different stages of maturation (including myelocytes, metamyelocytes, promyelocytes), an absolute basophilia, and, commonly, eosinophilia.
CML--1
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Aspirate smear Bone marrow evaluation shows increased cellularity due to granulocytic hyperplasia with a spectrum of maturation. Megakaryocytes in CML are characterized by decreased size and hypolobated nuclei ("dwarf megakaryocytes").
Chronic-Phase-CML--3
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Chronic-Phase-CML--2
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Chronic-Phase-CML--1
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Pseudo-Gaucher cells Pseudo-Gaucher cells and sea-blue histiocytes can be seen due to increased cell turnover.
PseudoGaucher-cells--4
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PseudoGaucher-cells--3
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Cytogenetics Chronic myelogenous leukemia is defined by the BCR-ABL1 fusion gene. Most cases have the characteristic t(9;22)(q34;q11.2) identified by routine cytogenetic analysis.
t922-Karyotype
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BCRABL-FISH
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Blast phase CML can progress to a blast phase defined by >20% blasts in the peripheral blood or bone marrow or by an extramedullary blast proliferation. The blast lineage may be myeloid or lymphoid.
Blast-Crisis-of-CML--5
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Blast-Crisis-of-CML--6
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Blast-Crisis-of-CML--12
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Blast-Crisis-of-CML--4
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