Try it
Pathology · Haematology: antithrombin deficiency
Sample itemA 28-year-old man has had two episodes of deep vein thrombosis, one in an unusual mesenteric vein. During treatment with intravenous unfractionated heparin, the aPTT stays near baseline even at high doses. Which inherited defect is most likely?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Antithrombin deficiency
Heparin acts by enhancing the activity of antithrombin, so patients with antithrombin deficiency show heparin resistance. It is autosomal dominant and carries a high risk of venous thrombosis.
Option by option
A. Antithrombin deficiency (correct)
Correct. Without adequate antithrombin, heparin cannot prolong the aPTT, giving heparin resistance.
B. Protein S deficiency
Protein S deficiency raises thrombosis risk through the protein C pathway without heparin resistance.
C. Factor V Leiden
Factor V Leiden causes activated protein C resistance but does not impair the heparin response.
D. Prothrombin G20210A variant
The prothrombin G20210A variant raises prothrombin level and thrombosis risk but not heparin resistance.
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.
More Pathology questions
- HaematopathologyBinucleate 'owl-eye' cells that stain for CD15 and CD30 are characteristic of which cond…
- NeuropathologyEosinophilic intracytoplasmic inclusions in the pigmented neurons of the substantia nigr…
- HaemodynamicsWhich of the following is NOT a component of Virchow's triad for thrombosis?
- Granulomatous diseaseNon-caseating granulomas with Schaumann bodies and asteroid bodies are typical of: