Risk factors, clinical features and treatment of Behçet's disease uveitis

Z Zhong, G Su, P Yang - Progress in Retinal and Eye Research, 2023 - Elsevier
Behçet's disease is a systemic vasculitis frequently associated with intraocular inflammation.
Recent findings identified independent clinical clusters in Behçet's disease, each involving …

Behcet's disease: A comprehensive review with a focus on epidemiology, etiology and clinical features, and management of mucocutaneous lesions

E Alpsoy - The Journal of dermatology, 2016 - Wiley Online Library
Behçet's disease (BD) is a chronic, relapsing, inflammatory multisystem disease of unknown
etiology. Oral ulcers, genital ulcers, cutaneous lesions, and ocular and articular involvement …

Behçet's disease: an overview of etiopathogenesis

P Leccese, E Alpsoy - Frontiers in immunology, 2019 - frontiersin.org
Behçet's disease (BD) is a systemic inflammatory disease with a chronic, relapsing-remitting
course of unknown etiology hallmarked predominantly by mucocutaneous lesions and …

Erythema nodosum: a practical approach and diagnostic algorithm

DM Pérez-Garza, S Chavez-Alvarez… - American journal of …, 2021 - Springer
Erythema nodosum is the most common form of panniculitis and is characterized by tender
erythematous nodules mainly in the lower limbs on the pretibial area. The exact cause of …

Consensus classification criteria for paediatric Behçet's disease from a prospective observational cohort: PEDBD

I Koné-Paut, F Shahram, M Darce-Bello… - Annals of the …, 2016 - ard.bmj.com
Background We aimed to describe the main features of Behçet's disease (BD) in children in
the largest prospective cohort to date and to propose a classification. Methods An …

Behçet disease: new aspects

I Bulur, M Onder - Clinics in dermatology, 2017 - Elsevier
Behçet disease is currently considered an “autoinflammatory disease” triggered by infection
and environmental factors in genetically predisposed individuals. Although the disease is …

Behçet's disease in children, an overview

I Koné-Paut - Pediatric Rheumatology, 2016 - Springer
BD is a systemic inflammatory disease with a variable vasculitis. Paediatric onset is very rare
and carries a strong genetic component. Oral ulcers and fever of unknown origin are …

Demographic and clinical properties of juvenile-onset Behçet's disease: A controlled multicenter study

Y Karincaoglu, M Borlu, SC Toker, A Akman… - Journal of the American …, 2008 - Elsevier
BACKGROUND: Behçet's disease (BD) is a multisystemic inflammatory disorder of unknown
origin. The disease usually occurs between the second and the fourth decades, whereas it is …

Behçet disease: evolution of clinical manifestations

H Ideguchi, A Suda, M Takeno, A Ueda, S Ohno… - Medicine, 2011 - journals.lww.com
Clinical phenotypes of Behçet disease (BD) vary among ethnic groups. We chronologically
analyzed the clinical manifestations of BD in 412 patients meeting the Japanese criteria for …

Treatment of Behçet's disease: an algorithmic multidisciplinary approach

E Alpsoy, P Leccese, G Emmi, S Ohno - Frontiers in medicine, 2021 - frontiersin.org
Behçet's disease (BD) is a chronic, relapsing inflammatory, multisystem disease of unknown
etiology. The disease has a wide clinical spectrum of mucocutaneous lesions and ocular …