Tuberculosis Masquerading as Behcet's Disease‐Pseudo Bechet's Syndrome: A Case‐Based Review of Literature [PDF]
Respirology Case ReportsBehcet's disease is a chronic, multisystem variable vessel vasculitis characterised by recurrent oral and genital ulcers, ocular inflammation and a wide range of systemic manifestations.
Rinoosha Rachel +4 more
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Atypical Pediatric‐Onset Behçet's Disease Presenting With Superior Vena Cava Thrombosis in an Adolescent Male: A Case Report [PDF]
Clinical Case ReportsBehçet's disease is a chronic, relapsing multisystem vasculitis known for its highly variable clinical spectrum. We report the case of an 18‐year‐old male who presented with progressive headache and facial swelling.
Ubaid Ullah +8 more
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Diagnosing neuro-Behçet’s disease [PDF]
Romanian Journal of Neurology, 2021 Behçet’s disease is a rare systemic vasculitis characterized by uveitis, recurrent oral and genital ulcers, firstly described by the turkish dermatologist Hulusi Behçet. The etiology is unknown, although autoimmune mechanisms are described.
Catalina Elena Bistriceanu +2 more
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Uveitis and Retinal Vasculitis—Harbingers of Neuro-Behcet’s Disease: A Case Report [PDF]
Bengal Physician Journal, 2023 We report this case of Neuro-Behcet’s disease who initially had recurrent episodes of uveitis over a period of 14 years and was under ophthalmological follow-up. Recently, she developed retinal vasculitis and multiple stroke-like episodes.
Pramod Kumar Samala +6 more
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Genetics of Behçet's Disease: Functional Genetic Analysis and Estimating Disease Heritability
Frontiers in Medicine, 2021 Behçet's disease is a chronic multisystemic inflammatory disorder characterized by recurrent oral and genital ulcers. Although its etiology remains unclear, it is thought that both genetic and environmental factors contribute to the onset and progression
Lourdes Ortiz-Fernández +4 more
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Evaluation of disease activity in uveoretinitis associated with Behçet’s disease
Immunological Medicine, 2021 Behçet’s disease is a multi-organ inflammatory disorder with systemic vasculitis of unknown etiology. Ocular lesions occur in about 70% of patients with Behçet’s disease, and it is more frequent and severe in men.
Hiroshi Keino
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Neutrophil and lymphocyte responses to oralStreptococcusin Adamantiades-Behçet's disease [PDF]
FEMS Immunology & Medical Microbiology, 2005 Immune reactions against microorganisms play an important pathogenic role in Adamantiades-Behçet's disease. We had previously obtained Streptococcus sanguinis (strain BD113-20), isolated from the oral cavity of patients with Adamantiades-Behçet's syndrome.
Kurauchi, Tomomi +7 more
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Cerebral pseudotumoral form of Behçet’s disease: About 3 cases
Interdisciplinary Neurosurgery, 2020 Behçet’s disease is a multisystem vasculitis which can involve the nervous system known as Neuro-Behçet’s disease. Neurological involvement is uncommon in Behçet’s disease, and has a highly variable prevalence.
Malek Mansour +4 more
doaj +1 more source
Blepharoptosis in Behçet's Disease [PDF]
Archives of Aesthetic Plastic Surgery, 2016 Behçet's disease is a systemic chronic disease that occurs in tissues such as eyes, joints, organs and nerves, and it has been noted that symptoms may be observed in a variety of tissues.
So-Min Hwang +4 more
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The acquisition of trisomy 8 associated with Behçet's-like disease in myelodysplastic syndrome
Leukemia Research Reports, 2020 A relationship has been reported between myelodysplastic syndrome (MDS) and autoimmune disease. Behçet's disease is a multisystem inflammatory disorder with mucocutaneous, articular, gastrointestinal, neurological, and vascular manifestations.
Satoko Oka, Kazuo Ono, Masaharu Nohgawa
doaj +1 more source