Table 1.
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.