1999
DOI: 10.1111/j.1600-0714.1999.tb02023.x
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Recurrent aphthous stomatitis in Behçet's disease: clinical featueres and correlation with systemic disease expression and severity

Abstract: A: Recurrent aphthous stomatitis in Behçet's disease: clinical features and correlation with systemic disease expression and severity. J Oral Pathol Med 1999; 28: 193-6. C Munksgaard, 1999. Behçet's disease (BD) is a multisystem disease, in which recurrent aphthous stomatitis (RAS) is a universal finding. We studied the expression of RAS in patients with BD, and the correlation between major or minor RAS and systemic expression and severity of the disease. Thirty-five patients with BD were studied, of whom… Show more

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Cited by 81 publications
(39 citation statements)
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“…This was used in 15/248 (6.0%) of published studies 38,46,51,57,104-114 . Several researchers used their own definition of disease severity 12,32,60,65,82,115,116,117 .…”
Section: Resultsmentioning
confidence: 99%
“…This was used in 15/248 (6.0%) of published studies 38,46,51,57,104-114 . Several researchers used their own definition of disease severity 12,32,60,65,82,115,116,117 .…”
Section: Resultsmentioning
confidence: 99%
“…For recurrent aphthous stomatitis, there was no relation between gender and types of aphthae. [13][14][15] According to the International Study Group (ISG) for Behçet's Syndrome diagnostic criteria, aphthae must recur more than three times a year for diagnosis of Behçet's syndrome. 16 Recurrent aphthous stomatitis also is seen in association with other conditions such as inflammatory bowel disease (IBD), celiac disease, hematinic deficiencies, systemic lupus erythematosus, reactive arthritis, formerly called Reiter's syndrome, mouth and genital ulcers with inflamed cartilage syndrome, cyclic neutropenia, and autoinflammatory diseases (familial Mediterranean fever, periodic fever, aphthous ulcers, pharyngitis, adenopathy, hyperimmunoglobulinemia D).…”
Section: Recurrent Aphthous Stomatitismentioning
confidence: 99%
“…All selected patients had aphthous lesions with at least two other clinical manifestations, such as genital ulcer, skin lesion (erythema nodosum, papulopustular lesion, folliculitis), positive pathergy reaction or ocular diseases (anterior or posterior uveitis). Disease activity was determined according to clinical signs and ranged from 1 to 3 (mild), 4 to 6 (moderate), and 7 to 9 (severe) according to Kruse et al [16,17]. The control group consisted of 44 healthy age-and sex-matched volunteers with no history of autoimmunity or significant severe infection at the time of sampling.…”
Section: Patient and Control Groupsmentioning
confidence: 99%