ArticleBMJ case reports2016
A rare case of Behçet disease with generalised myositis, cardiomyositis and necrotising fasciitis.
Article in BMJ case reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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Who cites it
4 citing papers in PubMed, 11 citations in OpenAlex.
- Gastrocnemius Myositis Associated with Behçet's Syndrome.European journal of case reports in internal medicine · 2023Article
- Muscular atrophy and weakness in the lower extremities in Behçet's disease: A case report and review of literature.World journal of clinical cases · 2021Article
- Recurrent myocarditis in the context of Behçet's disease: a case report.European heart journal. Case reports · 2021Article
- Atypical Behçet disease with endocarditis, pyoderma gangrenosum-like ulcers and methicillin-resistantJAAD case reports · 2018Article
Corrections and comments
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Authors and funding
4 authors at 4 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Behçet disease (BD) is a rare relapsing, multisystem vasculitis characterised by recurrent oral and genital ulcers, and uveitis. As an autoimmune small vessel vasculitis, BD can involve other organs including the skin, joints, nervous system, kidney and the gastrointestinal tract. This report describes a 40-year-old woman who presented with an uncommon feature of BD, namely myositis, and who went on to develop myocarditis and polymicrobial necrotising fasciitis. To the best of our knowledge, this is the first reported case of an immunocompromised-associated infection occurring in BD without concurrent immunosuppressive therapy.
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Registered trials
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