Results 31 to 40 of about 2,477 (110)

Primary Immunodeficiency Disease Mimicking Pediatric Bechet’s Disease

open access: yesChildren, 2021
Behcet’s disease (BD) is a chronic inflammatory disease with multisystemic involvement. Its etiology is considered to involve complex environmental and genetic factors. Several susceptibility genes for BD, such as human leukocyte antigen (HLA)-A26, IL23R-
Mayuka Shiraki   +4 more
doaj   +1 more source

The Role of Viral and Bacterial Infections in the Etiology of Behçet's Disease

open access: yesJournal of Clinical Laboratory Analysis, Volume 40, Issue 1, January 2026.
Bacterial and viral pathogens may play a key role in Behçet's disease (BD) pathogenesis by triggering autoimmunity, molecular mimicry, or microbiome disruption. These infectious agents could initiate inflammatory pathways, contributing to BD's diverse clinical manifestations.
Mohsen Moghoofei   +4 more
wiley   +1 more source

Tuberculosis Masquerading as Behcet's Disease‐Pseudo Bechet's Syndrome: A Case‐Based Review of Literature

open access: yesRespirology Case Reports, Volume 14, Issue 1, January 2026.
We report a case of recurrent oral/scrotal ulcers with systemic symptoms in a 33‐year‐old man masked pulmonary tuberculosis: imaging showed cavitary consolidations with effusion, and thoracoscopic pleural biopsy demonstrated acid‐fast bacilli. Anti‐tubercular therapy led to complete resolution, underscoring TB as a key Behçet's mimic to exclude before ...
Rinoosha Rachel   +4 more
wiley   +1 more source

Dactilitis and oligoarthritis after BCG immunotherapy in a patient affected by bladder cancer

open access: yesReumatismo, 2011
The treatment of bladder cancer with Bacillus of Calmette-Guerin (BCG) immunotherapy can induce the appearance of a reactive disorder. The Authors describe a 55-year-old male patient with bladder cancer treated with endovesical instillation of BCG ...
N. Elkhaldi   +4 more
doaj   +1 more source

Kikuchi–Fujimoto Disease Presenting With Complex Neurological Manifestations: A Case Report

open access: yesCase Reports in Neurological Medicine, Volume 2026, Issue 1, 2026.
Kikuchi–Fujimoto Disease (KFD) is a rare, typically self‐limiting inflammatory condition primarily associated with fever, cervical lymphadenopathy, and occasionally small‐vessel vasculitis. Central nervous system (CNS) involvement in KFD is exceedingly rare and has been described in isolated cases, including encephalitis, aseptic meningitis, and ...
Yusuf Kagzi   +5 more
wiley   +1 more source

Epidemiology of human leukocyte antigens among omani population

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2017
Oman is located on the Southeastern coast of the Arabian Peninsula, and its population has high levels of consanguinity. Human leukocytic antigen (HLA) typing analysis in human population holds unexploited potential for elucidating the genetic causes of ...
Issa Al Salmi   +6 more
doaj   +1 more source

Behçet‘s Syndrome Apart From the Triple Symptom Complex: Vascular, Neurologic, Gastrointestinal, and Musculoskeletal Manifestations. A Mini Review

open access: yesFrontiers in Medicine, 2021
Behçet‘s Syndrome (BS) is a variable vessel vasculitis according to the Chapel Hill Consensus Nomenclature (1) and may thus affect any organ, including major and minor arterial and venous vessels to a varying degree and with varying frequency.
Ina Kötter, Fabian Lötscher
doaj   +1 more source

Bilateral Neuroretinitis and a Unilateral Superior Hemivein Occlusion with Frosted Branch Angiitis Pattern Presenting Simultaneously in Behçet's Disease

open access: yesCase Reports in Ophthalmology, 2016
Purpose: To report a unique case of Behçet's disease that presented with atypical ocular manifestations. Methods: Case report. Results: A 23-year-old homosexual male presented with bilateral anterior uveitis, vitritis, neuroretinitis and a unilateral ...
Roy Schwartz   +6 more
doaj   +1 more source

Behçet’s Disease and Tuberculosis: A Complex Relationship

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2020
Behçet’s disease (BD) is a systemic vasculitis characterized by recurrent orogenital ulceration and several systemic manifestations (such as gastrointestinal involvement, vascular disease or arthritis).
Sara Mendonça Freitas   +4 more
doaj   +1 more source

Atypical Pediatric‐Onset Behçet's Disease Presenting With Superior Vena Cava Thrombosis in an Adolescent Male: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Behçet'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. Imaging revealed extensive thrombosis involving the dural venous sinuses, superior vena cava, and left brachiocephalic vein ...
Ubaid Ullah   +8 more
wiley   +1 more source

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