Results 21 to 30 of about 2,441 (231)

Comparison of histopathologic and clinical evaluations of pathergy test in Behçet’s disease

open access: closedInternational Journal of Dermatology, 2000
Abstract Background The pathergy test, an important test in the diagnosis of Behçet’s disease, is currently applied with disposable/sharp needles and evaluated only clinically (no histopathologic evaluation). In this study, the usefulness of the pathergy test conducted intradermally and intravenously with disposable/sharp needles in the diagnosis and ...
Özlem Akmaz   +2 more
openalex   +6 more sources

Induction of a Pathergy-Like Reaction Following Prick Skin Testing [PDF]

open access: bronzeJournal of Allergy and Clinical Immunology, 2006
Thomas L. Johnson   +4 more
openalex   +2 more sources

Usefulness of HLA determination and pathergy test in the diagnosis of uveitis in Turkey. [PDF]

open access: bronzeBritish Journal of Ophthalmology, 1981
Yılmaz Özyazgan   +7 more
openalex   +4 more sources

Uveitis and Retinal Vasculitis—Harbingers of Neuro-Behcet’s Disease: A Case Report [PDF]

open access: yesBengal 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
doaj   +1 more source

Diagnosing neuro-Behçet’s disease [PDF]

open access: yesRomanian 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
doaj   +1 more source

Pathergy-like reaction induced by laser hair removal in a patient with Behçet disease

open access: yesReumatismo, 2023
Behçet disease (BD) is a rare systemic vasculitis of unknown etiology, primarily characterized by recurrent oral aphthous ulcers, genital ulcers, uveitis, and skin lesions.
R. Nicolau, T. Martins Rocha, L. Costa
doaj   +1 more source

Case report: Deep vein thrombosis as the sole clinical feature of Behcet’s syndrome

open access: yesFrontiers in Medicine, 2023
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

Enhancing the Diagnosis of Behçet's Disease Using Machine Learning: A Comparative Study on Clinical Data From Saudi Arabia. [PDF]

open access: yesInt J Telemed Appl
Behçet’s disease (BD) is one of the most difficult diseases to diagnose in the field of rheumatic immune diseases because it is rare, has many different symptoms, and we do not know much about how it works. Instead of trying to make a direct clinical diagnosis, this study was set up as an exploratory investigation to find out more about BD and figure ...
Alalwany H   +7 more
europepmc   +2 more sources

Tuberculosis Masquerading as Behcet's Disease-Pseudo Bechet's Syndrome: A Case-Based Review of Literature. [PDF]

open access: yesRespirol Case Rep
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 ...
Rachel R   +4 more
europepmc   +2 more sources

Neuro-Bechet’s disease: a case series from India

open access: yesThe Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2022
Background There are several studies which have studied large cohort of Neuro-Bechet’s disease (NBD) patients worldwide However, there is sparse literature about NBD from India.
Rohan R. Mahale   +5 more
doaj   +1 more source

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