Case report: Deep vein thrombosis as the sole clinical feature of Behcet’s syndrome
IntroductionBehcet’s syndrome is a rare, chronic, systemic condition often categorized within the group of vasculitides. It presents a diagnostic challenge due to its varied clinical manifestations and the absence of a definitive laboratory test.
Abdelrahman Omara +7 more
doaj +1 more source
The seroprevalence and salivary shedding of herpesviruses in Behcet's syndrome and recurrent aphthous stomatitis [PDF]
This journal is published under the terms of the Creative Commons Attribution-NonCommercial 4.0 Unported ...
Bergmeier, LA +9 more
core +1 more source
The acquisition of trisomy 8 associated with Behçet's-like disease in myelodysplastic syndrome
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
Budd-chiari syndrome and renal arterial neurysms due to behcet disease: a rare association [PDF]
Behcet’s disease is a multisystemic vasculitis of unknown etiology with a chronic relapsing course. Vasculitis in Behcet’s disease with predominant vascular involvement is the only vasculitis that affects both arteries and veins of any size.
Dorum, M +3 more
core +1 more source
Immunosuppressants in Behcet’s disease: a boon or a bane? [PDF]
Adalimumab is a disease-modifying antirheumatic drug and monoclonal antibody that works by antagonising tumour necrosis factor-alpha prescribed in many rheumatological conditions like Rheumatic arthritis, Ankylosing spondylitis and Behcet’s disease ...
Shukla, Dhaiwat +3 more
core +1 more source
Budd-Chiari syndrome in association with Behçet's disease: review of the literature
The risk that patients with Behçet's disease may develop various thrombotic complications has been previously described. Although vascular complications from Budd-Chiari syndrome associated with Behçet's disease have been described, the pathogenic ...
Daniela Carvalho +3 more
doaj +1 more source
The authors present a male 40-year-old patient with established diagnosis of Behçet's disease which had evolved to recurrent bilateral auricular polychondritis crises.
Ana Claudia Mendes do Nascimento +3 more
doaj +1 more source
An Audit of Behcet’s Syndrome Research: A 10-year Survey
Objective.Data suggest that the use of disease control groups and proper use of power calculations were neglected in published reports. We surveyed these and other methodological shortcomings in reports published within the last decade about one specific
FEHIM ESEN +3 more
core +1 more source
Acute Eosinophilic Pneumonia in a Patient with Long Standing Behcet’s Syndrome [PDF]
Background: Behcet’s syndrome (BS) is a multisystemic disease that frequently manifests as oral and genital ulcers. Pulmonary involvement occurs in approximately 18% of patients and can have complex clinical manifestations, including vascular disease ...
Estefahani, Shadi J +3 more
core
Evaluation of the Thyroid Gland in Patients with Behcet’s Syndrome
Behcet’s Syndrome is a chronic, progressive, recurrent syndrome that can affect all organs and that histopathologically proceeds with vasculitis. Its etiology and pathogenesis is still unknown.
Yusuf Özkan +4 more
doaj +2 more sources

