Behçet disease in Latin American countries: A systematic literature review of demographic and clinical features, and HLA-B*51 allele frequency

Muñoz, Sebastián A.; Kostianovsky, Alex; Allievi, Alberto; Orden, Alberto O.

doi:10.1016/j.reumae.2022.12.005

Reumatología Clínica (English Edition)

2023

DOI: 10.1016/j.reumae.2022.12.005

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Behçet disease in Latin American countries: A systematic literature review of demographic and clinical features, and HLA-B*51 allele frequency

Sebastián A. Muñoz,

Alex Kostianovsky,

Alberto Allievi

et al.

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2024

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Fever, Leukocytosis, and Ulcerated Vulvar Lesions: An Atypical Presentation Concerning Behcet’s Disease

Patrick Eisenberg,

Pearce,

Anders

et al. 2024

Cureus

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Behcet’s disease (BD) is a variable-vessel vasculitis commonly presenting in early adulthood with painful oral aphthous ulcers, genital ulcers, uveitis, pathergy, and skin lesions. The diagnosis of BD is made clinically based on criteria from the International Study Group (ISG) and the International Criteria for Behcet’s Disease (ICBD). Due to the wide constellation of symptoms BD can cause, it can be challenging to diagnose in an acute setting. Here, we discuss a patient who presented with a clinical picture of sepsis, with profound ulcerated vulvar and herpetiform oral mucosal lesions, that led us to a presumptive diagnosis of Behcet’s disease.

show abstract

Fever, Leukocytosis, and Ulcerated Vulvar Lesions: An Atypical Presentation Concerning Behcet’s Disease

Patrick Eisenberg,

Pearce,

Anders

et al. 2024

Cureus

View full text Add to dashboard Cite

show abstract

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Behçet disease in Latin American countries: A systematic literature review of demographic and clinical features, and HLA-B*51 allele frequency

Cited by 1 publication

References 14 publications

Fever, Leukocytosis, and Ulcerated Vulvar Lesions: An Atypical Presentation Concerning Behcet’s Disease

Fever, Leukocytosis, and Ulcerated Vulvar Lesions: An Atypical Presentation Concerning Behcet’s Disease

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