ArticleCureus2026
Bilateral Renal Artery Thrombosis in a Patient With Behçet's Disease Managed With Infliximab Infusions.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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2 authors.
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Abstract
We present this rare case of bilateral renal artery involvement due to Behçet's disease (BD) vasculitis to attract the attention of clinicians. BD is a chronic autoimmune vasculitis affecting multiple organ systems. BD causes recurrent oral and genital aphthous ulcers, uveitis, papulopustular lesions, gastrointestinal ulcers, neurologic disease, vasculitis, and arthritis. We report the case of a 56-year-old male patient with 20 years of BD who developed renal artery thrombosis, diagnosed with acute renal failure, hypertension, abdominal bruit, and thoracoabdominal computed tomography angiography images showing bilateral renal artery thrombosis. Our patient was treated with steroids, colchicine, clopidogrel, antihypertensives, and infliximab infusions with clinical and laboratory improvement. Due to active inflammation, radiologic intervention was delayed until remission. We present this case of rare bilateral renal artery vasculitis to the attention of clinicians who take care of BD patients every day.
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