Leukaemia

Malaria (chronic, with splenomegaly), tropical splenomegaly syndrome, schistosomiasis, typhoid and brucellosis, tuberculosis, HIV and AIDS, lymphoma and leukaemia (chronic myeloid), histoplasmosis, and hepatosplenic causes such as chronic liver disease with portal hypertension.

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Study material on Leukaemia

Practice questions on Leukaemia

A 35-year-old patient is diagnosed with lymphoma. Biopsy reveals TdT-positive cells. The presentation overlaps significantly with acute lymphoblastic leukaemia. What is the diagnosis?

Answer: C. TdT (terminal deoxynucleotidyl transferase) positivity is the hallmark of lymphoblastic lymphoma — it is negative in ALL other NHL types. Treated with ALL protocols. ---

Which virus is associated with Adult T-cell Leukaemia/Lymphoma?

Answer: C. Human T-lymphotropic virus type 1 (HTLV-1) is the causative agent of Adult T-cell Leukaemia/Lymphoma. This is a must-know association. ---

Which BRAF mutation is present in >99% of Hairy Cell Leukaemia cases?

Answer: A. BRAF V600E mutation is present in >99% of hairy cell leukaemia cases, making it both diagnostic and a therapeutic target (vemurafenib). ---

A 62-year-old man presents with fatigue, fever and bruising. His full blood count shows WCC 40×10⁹/L with 25% circulating blasts, Hb 90 g/L and platelets 50×10⁹/L. Which investigation is required to definitively diagnose acute myeloid leukaemia?

Answer: A. Although the peripheral smear already shows circulating blasts, definitive diagnosis and subclassification of AML require bone marrow examination — combining morphology, cytochemistry, immunophenotyping, and cytogenetic/molecular analysis. ---

Which chromosomal translocation is pathognomonic of chronic myeloid leukaemia?

Answer: D. This is the Philadelphia chromosome, producing the BCR-ABL fusion gene that defines CML. The other options are characteristic translocations of specific AML/ALL subtypes, not CML.

Chronic lymphocytic leukaemia (CLL) is characterized by accumulation of

Answer: C. CLL is a clonal proliferation of functionally incompetent mature B cells (CD5+, CD23+, CD19+) that accumulate in blood, marrow, and lymph nodes. ---

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