## Immunophenotype of CLL **Key Point:** CLL is characterized by a unique immunophenotype: CD5+ CD19+ CD23+ B cells with dim surface immunoglobulin and CD79b expression. ### Diagnostic Immunophenotype | Marker | CLL | Mantle Cell | Marginal Zone | |--------|-----|-------------|---------------| | CD5 | + | + | − | | CD19 | + | + | + | | CD23 | + | − | − | | Surface Ig | Dim | Bright | Bright | | FMC7 | − | + | + | ### Clinical Significance - **CD5+ B cells:** Unusual co-expression of T-cell marker on B cells is the hallmark - **CD23+ status:** Distinguishes CLL from mantle cell lymphoma (CD23−) - **Dim surface Ig:** Indicates monoclonal B-cell population with restricted light chain (κ or λ) **High-Yield:** The CD5+ CD19+ CD23+ immunophenotype is sufficient for CLL diagnosis in the appropriate clinical context; no bone marrow biopsy required if peripheral blood shows >5,000 clonal B lymphocytes/μL. **Mnemonic:** **"CLL is CD5 CD19 CD23"** — remember all three are positive in CLL, unlike other B-cell lymphomas. **Clinical Pearl:** CD5+CD23− B-cell lymphocytosis suggests mantle cell lymphoma or marginal zone lymphoma, not CLL.
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