What are the classic findings of Chronic Lymphocytic Leukemia (CLL) on a Complete Blood Count (CBC)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: April 1, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

From the Guidelines

Chronic Lymphocytic Leukemia (CLL) is classically diagnosed on a Complete Blood Count (CBC) with lymphocytosis, typically showing an absolute lymphocyte count greater than 5,000 cells/μL, which is the primary diagnostic finding, as stated in the most recent guidelines 1. The diagnosis of CLL requires the presence of at least 5 × 10^9 B lymphocytes/L (5000/L) in the peripheral blood, with the clonality of the circulating B lymphocytes confirmed by flow cytometry 1.

Key Diagnostic Features

  • Lymphocytosis with an absolute lymphocyte count greater than 5,000 cells/μL
  • Small, mature-appearing lymphocytes with condensed nuclear chromatin, inconspicuous nucleoli, and scant cytoplasm
  • Characteristic "smudge cells" or "basket cells" (fragile lymphocytes that rupture during smear preparation)
  • Flow cytometry confirming a monoclonal B-cell population with the characteristic CLL immunophenotype (CD5+, CD19+, CD23+, dim surface immunoglobulin expression) 1

Additional Diagnostic Considerations

  • The presence of prolymphocytes in excess of 55% would favor a diagnosis of prolymphocytic leukemia (B-cell PLL) 1
  • CLL cells co-express the CD5 antigen and B-cell surface antigens CD19, CD20, and CD23, with low levels of surface immunoglobulin, CD20, and CD79b compared to normal B cells 1
  • Each clone of leukemia cells is restricted to expression of either λ or κ immunoglobulin light chains 1

From the Research

Chronic Lymphocytic Leukemia (CLL) Classic Findings on CBC

  • CLL is characterized by an increased number of B-lymphocytes in the blood, typically more than 5000 B-lymphocytes/µl 2
  • The diagnosis of CLL is established by blood counts, blood smears, and immunophenotyping of circulating B-lymphocytes, which identify a clonal B-cell population carrying the CD5 antigen as well as typical B-cell markers 3
  • Classic findings on CBC in CLL patients include:
    • Lymphocytosis (elevated lymphocyte count)
    • Anemia (low hemoglobin level)
    • Thrombocytopenia (low platelet count)
  • The European Binet staging system is used to classify CLL into three stages (A, B, and C) based on the degree of lymphadenopathy, organomegaly, and cytopenias 2
  • Patients with Binet stage A have 0 to 2 areas of node or organ enlargement with normal levels of hemoglobin and platelets, while those with Binet stage C have anemia and/or thrombocytopenia, with or without lymphadenopathy or organomegaly 2

Diagnostic Criteria

  • The diagnosis of CLL requires the presence of more than 5000 B-lymphocytes/µl in the blood, as well as the expression of specific surface markers such as CD5, CD19, and CD23 2, 3
  • Flow cytometry is used to confirm the diagnosis and to assess the expression of these surface markers 2, 3
  • Imaging studies such as X-ray, ultrasound, or CT scan may be used to assess the degree of lymphadenopathy or organomegaly 2

Prognostic Factors

  • The CLL international prognostic index integrates genetic, biological, and clinical variables to identify distinct risk groups of patients with CLL 3
  • Deletions of the short arm of chromosome 17 (del[17p]) and/or mutations of the TP53 gene predict resistance to chemoimmunotherapy and a shorter time to progression with most targeted therapies 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

[Chronic lymphocytic leukemia].

Deutsche medizinische Wochenschrift (1946), 2013

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.