Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/13719
Title: A rare case of Behçet disease with generalised myositis, cardiomyositis and necrotising fasciitis
Authors: Ng, Felix;Chiong, Fabian Joon Kiong;Buchanan, Russell R;Burrell, Louise M
Issue Date: 2016
Citation: BMJ Case Reports 2016; online first: 6 January
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.
URI: http://ahro.austin.org.au/austinjspui/handle/1/13719
DOI: 10.1136/bcr-2015-211983
PubMed URL: http://www.ncbi.nlm.nih.gov/pubmed/26740268
Type: Journal Article
Subjects: Behcet Syndrome
Myositis
Type of Clinical Study or Trial: Case Series and Case Reports
Appears in Collections:Journal articles

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