Behcet's disease. An update based on the 1985 International Conference in London

Jorizzo, Joseph L.

doi:10.1001/archderm.122.5.556

Cited by 37 publications

(7 citation statements)

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“…A single lesion of the brain stem confined to the periaqueductal grey matter between the levels of the superior and inferior colliculi results in ipsilateral oculomotor nerve palsy (7). The majority of isolated oculomotor nerve involvement has been reported as extraaxial lesions (4, 8).…”

Section: Discussionmentioning

confidence: 99%

A neuro-Behcet's lesion in oculomotor nerve nucleus

Aydın¹

2003

Acta Neurologica Scandinavica

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Section: Discussionmentioning

confidence: 99%

A neuro-Behcet's lesion in oculomotor nerve nucleus

Aydın¹

2003

Acta Neurologica Scandinavica

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“…Behcet disease should only be diagnosed in the absence of inflammatory bowel disease or autoimmune disease, the presence of ora! ulceratioE, and two or more of the following: genital ulceration, synovitis (migratory oonerosive oligoarthropathy), posterior uveitis, cutaneous pustular vasculitis, and meningoencephalitis (3)(4)(5). Unfortunately, none of the papulopustular lesions was biopsied, so pustular vasculitis cannot be excluded, but even so this girl did not satisfy these criteria.…”

Section: Discussionmentioning

confidence: 99%

Chronic Bullous Disease of Childhood and Ulcerative Colitis

Handley¹,

Shields²,

Dodge³

et al. 1993

Pediatric Dermatology

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A 12-year-old girl with ulcerative colitis (UC) treated by colectomy with rectal stump preservation, salazopyrin, and systemic steroids developed persistent mouth ulcers, cutaneous targetlike lesions, papulopustules, and bullae. The clinical, histologic, and immunopathologic features were typical of chronic bullous disease of childhood (CBDC). Although resistant to combined immunosuppressive therapy with low-dose prednisolone, cyclosporin, and thalidomide, striking remission of the mucocutaneous symptoms resulted with surgical resection of the diseased rectal stump. An etiologic association between CBDC and UC is postulated.

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“…There are three main sets of criteria for the diagnosis of Behcet's syndrome: the Barnes criteria, the Shimizu criteria adopted by the Behcet's Syndrome Research Committee of Japan, and the O'Duffy criteria. 16 The O'Duffy criteria are based on the six most common clinical manifestations. 2 It requires that three of the following six criteria be present: (1) recurrent aphthous stomatitis, (2) genital aphthous ulcers, (3) uveitis, (4) synovitis, (5) cutaneous vasculitis, and (6) meningoencephalitis.…”

Section: Discussionmentioning

confidence: 99%