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General Medicine · Haematology: aplastic anaemia
Sample itemA 19-year-old man has three weeks of fever and bleeding gums. Haemoglobin is 6 g/dL, white cells 1,200 per microlitre with an absolute neutrophil count of 300, and platelets 12,000. There is no splenomegaly or lymphadenopathy, and the marrow is hypocellular with fat replacement and no abnormal cells. His HLA-matched sibling is willing to donate. What is the treatment of choice?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Allogeneic haematopoietic stem cell transplantation from the matched sibling
Pancytopenia with a hypocellular fatty marrow and no infiltration or organomegaly is aplastic anaemia, here severe. In young patients with an HLA-matched sibling donor, stem cell transplantation offers cure and is the treatment of choice. Immunosuppression with ATG and ciclosporin is used for older patients or those without a donor.
Option by option
A. Allogeneic haematopoietic stem cell transplantation from the matched sibling (correct)
Correct. Transplant replaces the failed marrow and offers long-term cure in a young patient.
B. Antithymocyte globulin with ciclosporin as first choice
ATG with ciclosporin is the alternative when no matched donor exists or in older patients.
C. Repeated platelet transfusions and observation
Supportive transfusion alone does not treat marrow failure and carries high mortality.
D. Long-term prednisolone alone
Steroids do not restore marrow function in aplastic anaemia.
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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