Publication:
Management of vascular Behcet's disease

dc.contributor.authorsAlibaz-Oner, Fatma; Direskeneli, Haner
dc.date.accessioned2022-03-10T15:25:32Z
dc.date.accessioned2026-01-11T18:03:43Z
dc.date.available2022-03-10T15:25:32Z
dc.date.issued2019
dc.description.abstracty Behcet's disease (BD) is a chronic, multisystemic, inflammatory disease characterized by recurrent attacks of mucocutaneous, ocular, musculoskeletal, vascular, central nervous system and gastrointestinal manifestations. Treatment of BD changes according to organ involvement, gender and age of the patient with no golden standard therapeutic regimen. Vascular involvement is observed in up to 40% of the patients with BD, especially in young males and is one of the major causes of mortality and morbidity. Glucocorticoids, azathioprine and cyclophosphamide are still recommended as the first-line treatments in vascular BD. However, increasing data with the tumor necrosis factor inhibitors suggest that these agents may also be acceptable options for the management of refractory vascular BD in daily practice. Anticoagulant usage for vascular BD is also still controversial with limited data coming from retrospective studies. There is a clear need for randomized, controlled studies for the management of VBD.
dc.identifier.doi10.1111/1756-185X.13298
dc.identifier.eissn1756-185X
dc.identifier.issn1756-1841
dc.identifier.pubmed29665281
dc.identifier.urihttps://hdl.handle.net/11424/220280
dc.identifier.wosWOS:000618346300017
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofINTERNATIONAL JOURNAL OF RHEUMATIC DISEASES
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBehcet's disease
dc.subjectTNF inhibitors
dc.subjectvascular involvement
dc.titleManagement of vascular Behcet's disease
dc.typereview
dspace.entity.typePublication
oaire.citation.endPage108
oaire.citation.startPage105
oaire.citation.titleINTERNATIONAL JOURNAL OF RHEUMATIC DISEASES
oaire.citation.volume22

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