Differential Diagnosis for a 75-year-old man with consistent lymphocytosis
Single most likely diagnosis
- Chronic Lymphocytic Leukemia (CLL): This is the most likely diagnosis given the patient's age and the presence of consistent lymphocytosis with flow cytometry showing only lymphocytes. CLL is a common cause of lymphocytosis in older adults and often presents with a prolonged history of lymphocytosis.
Other Likely diagnoses
- Monoclonal B-cell Lymphocytosis (MBL): This condition is characterized by the presence of small clones of B cells and can be considered a precursor to CLL. It's a possible diagnosis given the flow cytometry results showing only lymphocytes.
- Reactive Lymphocytosis: Although less likely given the chronic nature of the lymphocytosis, reactive lymphocytosis due to chronic infection or inflammation could be considered, especially if other causes are not identified.
Do Not Miss (ddxs that may not be likely, but would be deadly if missed.)
- Lymphoma (e.g., Mantle Cell Lymphoma, Follicular Lymphoma): Although less common than CLL, other types of lymphoma could present with lymphocytosis and would require prompt diagnosis and treatment.
- Hairy Cell Leukemia: A rare type of leukemia that can present with lymphocytosis and splenomegaly, requiring specific treatment.
- Large Granular Lymphocyte (LGL) Leukemia: A rare disorder that can cause lymphocytosis and has implications for immune function and potential transformation.
Rare diagnoses
- Adult T-cell Leukemia/Lymphoma (ATL): Caused by the human T-lymphotropic virus (HTLV-1), this is a rare condition in most parts of the world but should be considered in endemic areas or in patients with risk factors.
- Sezary Syndrome: A cutaneous T-cell lymphoma that can present with lymphocytosis, although it typically involves skin manifestations.
- Prolymphocytic Leukemia: A rare and aggressive leukemia that can present with high levels of lymphocytosis and typically has a poor prognosis.