1. Double whammy: anticoagulant-related nephropathy with leukocytoclastic vasculitis due to warfarin
- Author
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Vinant Bhargava, DS Rana, Vaibhav Tiwari, Anil Kumar Bhalla, Ashwani Gupta, Anurag Gupta, Pallav Gupta, Gaurav Bhandari, and Manish Malik
- Subjects
Male ,Vasculitis ,Nephrology ,medicine.medical_specialty ,Pathology ,medicine.medical_treatment ,Case Report ,Nephropathy ,Renal Dialysis ,Internal medicine ,Biopsy ,medicine ,Humans ,Dialysis ,medicine.diagnostic_test ,business.industry ,Acute kidney injury ,Warfarin ,Anticoagulants ,General Medicine ,Middle Aged ,medicine.disease ,Skin biopsy ,Vasculitis, Leukocytoclastic, Cutaneous ,Female ,business ,medicine.drug - Abstract
Anticoagulation-related nephropathy (ARN) is a rare form of acute kidney injury where the use of anticoagulation causes hemorrhage in various compartments of nephron including glomerulus, renal tubules, and interstitial compartment. Also, warfarin-induced vasculitis is an extremely rare condition characterized by the appearance of purpuric lesions on the skin which on biopsy are suggestive of leukocytoclastic vasculitis (LV). We hereby report a case presenting with coexistent warfarin-induced nephropathy and cutaneous vasculitis. A 64-year-old male, on warfarin for 10 years, presented with complaints of palpable purpuric rashes over lower limbs, hematuria, and decrease urine output. INR was in the supratherapeutic range (INR-6.3). Skin biopsy of the lesion was suggestive of LV and kidney biopsy showed RBCs in Bowman’s capsule, RBCs and RBC casts in tubules suggestive of ARN. All vasculitic markers were negative. Thus, a diagnosis of warfarin-induced nephropathy and cutaneous vasculitis was made. Warfarin was discontinued and oral steroids were started. Gradually, his skin lesions improved, and he became dialysis independent. He was then discharged on apixaban. On follow-up after 3 months, his skin lesions had disappeared with partial recovery of kidney function (cr-5.49).
- Published
- 2021
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