Leukemias Overview: ALL, CML, AML, APML, CLL
Acute leukemias > 20% blasts in the peripheral blood smear or on bone marrow leading to a more rapid onset of symptoms.
Chronic leukemia < 20% blasts with a relatively chronic onset of symptoms.
ALL (Acute Lymphoblastic Leukemia):
• Lymphocytes - T or B lineage
• Immature
• Age: 10
• 75% usually under 6 years age
• 75% of ALL is of B-cell lineage
ALL Symptoms:
• Malaise, bleeding, infections, bone pain
• Bulky lymphadenopathy
• Blast cells - Blood and Bone marrow
• Mature B-cell ALL can present as extramedullary disease, including gastrointestinal or testicular involvement
• T-cell ALL: mediastinal mass
• Rapidly rising blast cells - Blood & BM
• Bulky lymphadenopathy
• Cytopenia -> BM involvement
• 30%: CNS involvement
CML (Chronic Myeloid Leukemia):
• Neutrophils (myeloid)↑
• Mature
• Age: 40-60
• + (9;22) Philadelphia - BCR-ABL
• ↑ Tyrosine Kinase activity
• ↓ LAP Score
• CML -> AML: Blast crises
• Blasts > 10% leukocytes
Blast Phase:
• Headaches, bone pain, fever, joint pain, bleeding, infections, and lymphadenopathy
CML Findings:
• Splenomegaly
• ↑ Leukocyte count ↑ PLT
• ↑ PBS: Granulocytic cells in all phases of maturation
• (Peripheral eosinophilia, basophilia, and thrombocytosis)
CML Symptoms:
• Fatigue, weight loss, abdominal fullness (splenomegaly), night sweats, bleeding
• Pruritis after hot bath/showers
• Lymphadenopathy
AML (Acute Myeloid Leukemia):
• Neutrophils
• Immature/Myeloblasts
• Age: 50-60
• Auer Rods
Significant ↓ PLT: Petechiae, bruising, bleeding, infection
RARE - Lymphadenopathy/HSM
Leukocyte Count:
• ↑ Can develop leukostasis syndrome: CNS manifestations, hypoxia, CXR - infiltrates (anemia, thrombocytopenia, or functional neutropenia)
• Bone pain, dyspnea, gingival hypertrophy
• Leukemia cutis (violaceous, nontender cutaneous plaques)
AML Dx:
• ↑ Leukocyte count
• ↓Hg & PLT
• Peripheral smear: Blasts
APML (Acute Promyelocytic Leukemia):
• Poorly differentiated leukocytes + distinctive primary granules
• t(15;17) translocation
• Significant bleeding: Fibrinolysis & DIC
• Tumor lysis syndrome: Develops in treated pts. Intracellular Urate, Potassium and Phosphorus
CLL (Chronic Lymphocytic Leukemia):
• Lymphocytes
• Mature
• Age: 60-80
Clonal Accumulation of Mature B Lymphocytes:
• In the peripheral blood, bone marrow and secondary lymphoid organs
When Cancer Cells are in the Lymph Nodes:
• Small lymphocytic lymphoma (SLL)
CLL Symptoms:
• Lymphadenopathy
• HSM
• Fevers
• Drenching night sweats/fatigue
• Exaggerated response to mosquito bites
CLL -> Invade Skin: Leukemia cutis
Labs:
• Lymphocytosis/Cytopenias
• AIHA, ITP, Agranulocytosis
• Hypogammaglobulinemia, smudge cells
Richter's Transformation:
• Complication of Chronic Lymphocytic Leukemia (CLL) and/or Small Lymphocytic Lymphoma (SLL)
• Sudden transformation of the CLL/SLL into a significantly more aggressive form of large cell lymphoma
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