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Pathology · Haematology: CLL complication
Sample itemA 68-year-old man with known chronic lymphocytic leukaemia has new fatigue and jaundice. Haemoglobin has fallen from 12 to 7.5 g/dL, reticulocytes are 9 percent, the smear shows spherocytes and the direct Coombs test is positive for IgG. What is the diagnosis?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
D. Warm autoimmune haemolytic anaemia complicating CLL
Autoimmune haemolytic anaemia, usually of the warm IgG type, is a recognised complication of CLL, and the high reticulocyte count, spherocytes and positive Coombs test establish it. Treatment is with corticosteroids, and treatment of the underlying CLL if needed. Pure red cell aplasia also occurs in CLL, but reticulocytes are very low.
Option by option
A. Marrow replacement by leukaemic cells
Marrow infiltration gives a low reticulocyte count with a leukoerythroblastic or cytopenic picture.
B. Richter transformation to diffuse large B-cell lymphoma
Richter transformation presents with rapid node growth, fever and raised LDH, not primarily with Coombs-positive haemolysis.
C. Pure red cell aplasia
Pure red cell aplasia gives a very low reticulocyte count and a negative Coombs test.
D. Warm autoimmune haemolytic anaemia complicating CLL (correct)
Correct. Reticulocytosis, spherocytes and IgG on red cells establish immune haemolysis.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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