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. Author manuscript; available in PMC: 2017 Jan 25.
Published in final edited form as: Hematology Am Soc Hematol Educ Program. 2015;2015:264–271. doi: 10.1182/asheducation-2015.1.264

Table 1.

Summary of 2008 WHO diagnostic criteria

Chronic myeloid leukemia* (chronic phase) Atypical chronic myeloid leukemia Chronic neutrophilic leukemia
Blood
 WBC nd >13 × 10e9/L >25 × 10e9/L
 Neutrophils and bands nd nd >80%
 Immature granulocytes ≥10% ≥10% <10%
 Basophilia Present Minimal or <2% of leukocytes nd
 Myeloblasts Usually <2% <20% <1%
Marrow
 Granulocytic hyperplasia Present Present Present
 Myeloblasts Usually <5% <20% <5%
 Granulocytic dysplasia Minimal/absent Prominent Minimal/absent
 Megakaryocytic dysplasia Usually present* May or may not be present Minimal/absent
Other
 Hepatosplenomegaly nd nd Present
BCR-ABL or variant transcripts Present Absent Absent
PDGFRA, PDGFRB, or FGFR1 rearrangements Absent Absent Absent
 PV, PMF, or ET by WHO criteria No No No
 Monocytosis >1 × 10e9/L Absent Absent Absent

nd, not defined.

*

90%–95% have the t(9;22)(q34;q11.2) there are rare cases of variant translocations or cryptic translocations; absolute basophilia is invariably present and eosinophilia is common. Small, hypolobated megakaryocytes (“dwarf megakaryocytes”) are usually present.

In the absence of a clonal cytogenetic or molecular marker, rule out reactive neutrophilia and an underlying tumor.

Promyelocytes, myelocytes, and metamyelocytes.