2021
DOI: 10.1097/bor.0000000000000847
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Updates in cutaneous manifestations of systemic vasculitis

Abstract: Purpose of reviewThe main purpose of this review is to present newly reported cutaneous manifestations of systemic vasculitis, updates in investigations to verify systemic involvement in cases with cutaneous vasculitis and new therapeutic guidelines. The spectrum of COVID-19-related vasculitis is also covered. Recent findingsOnly a few reports highlighted new cutaneous presentations or associations with some systemic vasculitic entities. For example, the association of inflammatory disorders with Takayasu arte… Show more

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Cited by 8 publications
(6 citation statements)
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“…TAK causes mainly LVV and MVV of the larger medium-sized arteries, including the CNS [ 19 , 21 , 22 ]. Because retinal and skin vasculitis can occur, rare SVV manifestations should be considered [ 11 , 118 ].…”
Section: The Primary Vasculitidesmentioning
confidence: 99%
“…TAK causes mainly LVV and MVV of the larger medium-sized arteries, including the CNS [ 19 , 21 , 22 ]. Because retinal and skin vasculitis can occur, rare SVV manifestations should be considered [ 11 , 118 ].…”
Section: The Primary Vasculitidesmentioning
confidence: 99%
“…Behcet’s Disease (BD) is a systemic vasculitis of unknown etiology involving different-sized vessels presenting between the second and fourth decades of life with a higher prevalence around the historical Silk Road. Since various organs may be involved, use of appropriate imaging modalities is mandatory for the assessment of disease extent [ 40 , 41 ]. BD is marked by recurring oropharyngeal ulcers, genital ulcers, and ocular involvement.…”
Section: Autoimmune/inflammatory Disorders and Vasculitidesmentioning
confidence: 99%
“…Genital ulcers are smaller and occur less frequently. Other common cutaneous lesions include erythema-nodosum-like nodules, pseudofolliculitis, papulopustular lesions, acneiform nodules, and superficial thrombophlebitis ( Figure 7 C,D) [ 41 , 42 ].…”
Section: Autoimmune/inflammatory Disorders and Vasculitidesmentioning
confidence: 99%
“…In patients with CV, radiological and laboratory evaluations should be performed to investigate systemic involvement [ 4 ]. Since histopathological diagnosis takes time, many patients with clinical suspicion of CV are exposed to unnecessary laboratory examinations or immunosuppressive therapies.…”
Section: Introductionmentioning
confidence: 99%