History and exam

Key diagnostic factors

common

splenomegaly

Extramedullary hematopoiesis is the likely cause.

fatigue

Due to anemia, hyperviscosity, or multifactorial etiology.

malaise

Due to anemia, hyperviscosity, or multifactorial etiology.

night sweats

Due to leukotriene release.

fever

Can be due to neutropenic infection.

abnormal/excessive bleeding

Likely related to thrombocytopenia or platelet dysfunction.

bone pain

Due to bone marrow invasion.

Other diagnostic factors

common

weight loss

Due to anorexia or early satiety from splenomegaly.

petechiae, ecchymoses, or easy bruising

Due to thrombocytopenia or platelet dysfunction.

infection

A more common feature of blast-phase chronic myeloid leukemia (CML) than chronic- or accelerated-phase CML.

Nonspecific in nature and corresponds to any form of leukopenia.

abdominal pain

Sequela of splenomegaly.

uncommon

visual changes

Disease may present as retinal hemorrhages or retinal vessel occlusion.

focal neurologic signs

Stroke may be a manifestation of peripheral blood hyperviscosity.[33][34][35]

priapism

May be a manifestation of peripheral blood hyperviscosity.[36][37]

tinnitus

May be a manifestation of peripheral blood hyperviscosity.

confusion or stupor

Peripheral blood hyperviscosity or multifactorial etiology.

Risk factors

strong

history of chronic myeloid leukemia (CML)

If untreated, CML will progress to fatal blastic disease within 3-5 years.[8]​​ Less than 5% of CML patients present in an advanced phase, although some patients will progress to accelerated or blast phase despite treatment.[9]​ In one study, 10-year cumulative incidence of transformation to the blast phase was 5.8% for patients with chronic-phase CML treated with imatinib as initial therapy; most transformations occurred in the first 2 years from diagnosis.[10]

Risk factors for progression of chronic phase CML to blast crisis include intolerance or resistance to tyrosine kinase inhibitors and lack of adherence to treatment.[17]

Additional chromosomal abnormalities (ACAs) and somatic mutations are acquired during the course of CML. High-risk ACAs (e.g., i(17)(q10), −7/del7q, and 3q26.2 rearrangements) and high-risk somatic mutations (e.g., ASXL1 and ABL1 kinase domain mutations) are associated with progression to blast phase and poor prognosis.[19][20]

exposure to alkylating chemotherapeutic agents

Patients with CML treated with older alkylating agents (primarily busulfan) may develop blast crisis quickly.[13]​​

weak

exposure to ionizing radiation

Case series and literature reviews report secondary CML following radiation therapy.[21][22][23]

A positive association exists between cumulative dose of ionizing radiation and death caused by CML among nuclear industry workers.[14][15]

​An increased incidence of CML has been reported in Japanese atomic bomb survivors; risk appears to be greater with exposure to higher-radiation doses.[24]

Use of this content is subject to our disclaimer