II. Epidemiology
- Chronic Leukemia is primarily an adult chronic cancer (esp. over age 65 years)
IV. Symptoms
- Asymptomatic at presentation (incidentally diagnosed based on CBC with Leukocytosis)- Chronic Lymphocytic Leukemia- Asymptomatic at diagnosis: 50%
 
- Chronic Myelogenous Leukemia- Asymptomatic at diagnosis: 20%
 
 
- Chronic Lymphocytic Leukemia
- Symptomatic Patients- Symptoms are much less common in Chronic Leukemia than with Acute Leukemia)
- Constitutional symptoms
 
V. Signs
- Splenomegaly (46 to 76% of CML cases)
- Hepatomegaly (CLL or CML)
- Lymphadenopathy (CLL or CML)
VI. Labs
- 
                          Complete Blood Count (both CLL and CML)- Leukocytosis (or Hyperleukocytosis)- White Blood Cell Count is >20,000/mm3 in most cases, and often >100,000/mm3 (Hyperleukocytosis)
- Contrast with normal white cell counts or Leukopenia associated with Acute Leukemias
 
 
- Leukocytosis (or Hyperleukocytosis)
- 
                          Chronic Lymphocytic Leukemia (CLL)- Significant increase of normal appearing Lymphocytes (>50% of cells)
- Peripheral blood for clonal expansion of B Lymphocytes >5000/mm3, and confirmed by flow cytometry
- Bone Marrow Biopsy is not needed for diagnosis (but defines extent of marrow involvement related to prognosis)
 
- 
                          Chronic Myelogenous Leukemia (CML)- Peripheral Smear with few blast cells and increased Basophils and Eosinophils
- Philadelphia Chromosome (BCR-ABL1 Fusion Gene) on peripheral blood or Bone Marrow testing- Present in 90 to 95% of CML cases
- Also present in ALL (2-4% of children, 20-40% of adults)
 
 
