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Allergic medication reaction
1%
1/70
Hereditary disorder
11%
8/70
Neisseria meningitidis
6%
4/70
Septic emboli
64%
45/70
Superficial vein thrombosis
16%
11/70
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This patient is presenting with leg pain and a necrotic patch on their leg after starting warfarin (without heparin being given) and is most likely experiencing warfarin-induced skin necrosis. This condition often occurs in patients who have protein C deficiency (a hereditary disorder). Warfarin-induced skin necrosis presents with pain, bulla formation, and skin necrosis following initiation of warfarin. The major risk factor is protein C deficiency. Warfarin inhibits the production of proteins C/S (anticoagulants) as well as clotting factors IX, X, VII, and II. It depletes proteins C and S first, thus patients may experience a transient hypercoagulable state when starting warfarin (which is why heparin is given until the patient has a therapeutic INR). Patients with protein C/S deficiency are even at greater risk for warfarin skin necrosis given they already have low protein C/S levels. Heparin is used for anticoagulation in these patients. Figure A displays an example of warfarin-induced skin necrosis of the lower limb with the classic necrotic skin lesion. Incorrect Answers: Answer 1: Allergic medication reaction may present with urticaria or edema of the upper airway. Warfarin skin necrosis is not an allergic reaction. Answer 3: Neisseria meningitidis may cause a purpuric rash when disseminated as well as would present with a fever, hypotension, tachycardia, and adrenal failure. Answer 4: Septic emboli may be seen in bacterial endocarditis and could present with septic pulmonary emboli in the lungs (cough and fever) or the lower extremities (severe pain). Answer 5: Superficial vein thrombosis may present with a tender and palpable vein over the lower extremity. This pathology could possibly cause a pulmonary embolism (though it is less likely when compared to a DVT). Bullet Summary: Protein C/S deficiency can predispose patients to warfarin skin necrosis.
4.2
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