08/05/2025
APPROACH TO LEUKEMIA
🔬 When a patient presents with constitutional symptoms (fever, chills, night sweats, weight loss) + hepatosplenomegaly, always think:
CBC + Peripheral Smear → Blasts on smear?
Let’s break it down:
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⚡ Step 1: Lymphoid vs Myeloid Lineage?
Use flow cytometry and morphology.
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☄️ Lymphoid Leukemias:
Acute Lymphoblastic Leukemia (ALL)
→ Bone marrow biopsy: >20% lymphoblasts
→ Assess for Philadelphia chromosome
→ ✅ If positive: Dasatinib/Nilotinib + HSCT
→ 🧪 Treat with Hyper-CVAD (multi-agent chemo)
Textbook tip: Most common in children. Good prognosis with early treatment!
Hairy Cell Leukemia
→ Seen with leukopenia, and “hairy” projections on smear
→ Treat with Cladribine
Rare B-cell leukemia, often presents with splenomegaly and pancytopenia
Chronic Lymphocytic Leukemia (CLL)
→ Mature lymphocytosis + smudge cells on smear
→ CD5/CD23+ B-cells confirmed by flow cytometry
→ Treat with Fludarabine + Chlorambucil
Watchful waiting in asymptomatic patients is appropriate
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🔥 Myeloid Leukemias:
Acute Myeloid Leukemia (AML)
→ Bone marrow biopsy: >20% myeloblasts
→ Treat with 7+3 (cytarabine + anthracycline), ± HSCT
Classically seen in older adults. Auer rods on smear are hallmark!
Acute Promyelocytic Leukemia (APL)
→ Atypical promyelocytes on smear
→ Treat with ATRA (All-Trans Retinoic Acid)
→ Medical emergency due to DIC risk
Associated with t(15;17) translocation
Chronic Myeloid Leukemia (CML)
→ WBC >100,000, granulocytes on smear
→ Confirm with Philadelphia chromosome (t(9;22)) via FISH
→ Treat with Tyrosine Kinase Inhibitors (Imatinib/Dasatinib)
→ If in blast crisis: Add HSCT
Triphasic disease: chronic → accelerated → blast phase
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📌 High-Yield Notes:
1.Always differentiate acute vs chronic by blast percentage
2.Philadelphia chromosome is present in both CML and Ph+ ALL
3.CLL is the most common leukemia in elderly adults
4.AML is associated with benzene exposure and prior chemo
5.APL needs urgent ATRA due to high coagulopathy ris