## Peripheral Blood Smear in CML Chronic Phase ### Definition and Characteristics **Key Point:** CML chronic phase is defined by: - <5% blasts in peripheral blood - <5% blasts in bone marrow - <30% basophils + eosinophils combined - Presence of Philadelphia chromosome (BCR-ABL1) ### Expected Findings in Chronic Phase | Finding | Mechanism | Presence in Chronic Phase | |---------|-----------|---------------------------| | **Left shift (myelocytes, metamyelocytes, bands)** | Uncontrolled myeloid proliferation | Yes, hallmark | | **Basophilia** | Increased basophil count; part of myeloid expansion | Yes, common | | **Eosinophilia** | Increased eosinophil count; part of myeloid expansion | Yes, common | | **Blasts <5%** | Controlled proliferation in chronic phase | Yes, by definition | | **Toxic granulations** | Cytoplasmic abnormalities; may be present | Yes, possible | | **Döhle bodies** | Cytoplasmic inclusions of ribosomes; may be present | Yes, possible | | **Blasts >30%** | Indicates acceleration or blast crisis | **NO — this defines accelerated phase/blast crisis** | ### Why >30% Blasts is NOT Chronic Phase **High-Yield:** Blast crisis (or accelerated phase with >30% blasts) represents **progression** from chronic phase and is defined by: - ≥30% blasts in blood or marrow (blast crisis) - 20–29% blasts = accelerated phase - These are separate phases with worse prognosis **Clinical Pearl:** The presence of >30% blasts **disqualifies the diagnosis of chronic phase** — it indicates the patient has progressed to blast crisis, which requires escalation of therapy (e.g., tyrosine kinase inhibitor intensification or stem cell transplant). **Mnemonic:** **CML Phases by Blast %** - **Chronic:** <5% blasts - **Accelerated:** 5–29% blasts (or other criteria) - **Blast Crisis:** ≥30% blasts ### Toxic Changes in CML **Key Point:** Toxic granulations and Döhle bodies reflect cytoplasmic stress and are **not specific to CML** but can occur in severe infections, sepsis, and myeloproliferative disorders.
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