Mucocutaneous manifestations of Behçet's disease.
Behçet's disease is a relapsing multisystem polysymptomatic disease with exacerbations and remissions defined by the presence of the major symptom, recurrent oral aphthous ulcers, plus two of the following: recurrent genital ulceration, eye lesions, skin lesions or a positive pathergy test. Mucocuta...
| Publicado en: | Acta Reumatológica Portuguesa Vol. 38; no. 2; pp. 77 - 91 |
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| Autores principales: | , , , , |
| Formato: | Artículo |
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Sociedade Portuguesa de Reumatologia
abr-jun2013
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| Acceso en línea: | Ver este registro en EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=lth&AN=89335998&site=ehost-live header: @attributes: shortDbName: lth uiTerm: 89335998 longDbName: MedicLatina uiTag: AN controlInfo: bkinfo: jinfo: jid: 0303464X 4Z1D jtl: Acta Reumatológica Portuguesa issn: 0303464X maglogo: N pubinfo: dt: abr-jun2013 vid: 38 iid: 2 pid: 38819 pub: Sociedade Portuguesa de Reumatologia artinfo: ui: 89335998 ppf: 77 ppct: 14 formats: fmt: @attributes: type: P size: 11.7MB tig: atl: Mucocutaneous manifestations of Behçet's disease. aug: au: Uva, Luís Miguel, Diana Pinheiro, Catarina Filipe, Paulo Pedro Freitas, João affil: Clínica Universitária de Dermatologia, Faculdade de Medicina de Lisboa, Portugal su: Behçet's disease Disease exacerbation Disease relapse Canker sores Mouth ulcers Tissue wounds Precancerous conditions sug: subj: Behçet's disease Disease exacerbation Disease relapse Canker sores Mouth ulcers Tissue wounds Precancerous conditions keyword: Behçet's disease Cutaneous manifestations Diagnostic criteria Epidemiology Etiopathogenesis Treatment ab: Behçet's disease is a relapsing multisystem polysymptomatic disease with exacerbations and remissions defined by the presence of the major symptom, recurrent oral aphthous ulcers, plus two of the following: recurrent genital ulceration, eye lesions, skin lesions or a positive pathergy test. Mucocutaneous manifestations like oral and genital ulcers, and cutaneous lesions (papulopustular lesions, erythema nodosum-like lesions, cutaneous ulcers, superficial thrombophlebitis) are considered the "fingerprint" of the disease, being the most common and often the first signs to appear. Although the exact etiopathogenesis is still not known, genetic predisposition and environmental factors may influence and contribute to the development of this disease. Diagnosis is based on the International Study Group criteria. During the last years, this disease has been largely studied and new immunological data and treatment strategies have been postulated. Despite that, further studies and attention to new data are needed. pubtype: Academic Journal doctype: Article src: R language: English refInfo: copyright: @attributes: flag: Y custom: Copyright of Acta Reumatológica Portuguesa is the property of Sociedade Portuguesa de Reumatologia and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. item: Acta Reumatológica Portuguesa holder: Sociedade Portuguesa de Reumatologia dt: @attributes: year: 2013 holdings: @attributes: islocal: N |
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