Results 41 to 50 of about 2,246 (155)
Siriraj Medical Journal, 2020 Objective: To evaluate the clinical, histopathological, and immunopathological findings of the pathergy test in Thai patients with Behcet's disease. Methods: A pathergy test using the needle prick method with a 20G disposable needle after cleaning with ...
Nittaya Phanuphak +3 more
doaj
The Role of Viral and Bacterial Infections in the Etiology of Behçet's Disease
Journal 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
Anti-p200 pemphigoid (anti-laminin-γ1 pemphigoid) demonstrating pathergy
International Journal of Women's Dermatology, 2015 Anti-p200 pemphigoid, also called anti-laminin-γ1 pemphigoid, is a recently defined entity. First reported in 1996, the incidence is relatively rare, with approximately 70 reports in the literature. Clinical presentation is heterogeneous, but the disease
Morgan McCarty, DO +2 more
doaj +1 more source
Medical Mycology Case Reports, 2020 Purpureocillium lilacinum is a rare but emerging pathogen in immunocompromised patients that primarily infects the skin and subcutaneous tissue. We present a novel case of Purpureocillium lilacinum infection in a patient with pyoderma gangrenosum who was
Julia Accetta +5 more
doaj +1 more source
Giant cellulitis‐like Sweet's syndrome induced by gilteritinib
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Juan de Luque‐Fernández +5 more
wiley +1 more source
Vascular Behçet’s Disease: A Case of Arterial Occlusion and Successful Medical Management
Case Reports in Medicine, Volume 2026, Issue 1, 2026.Behçet’s disease is a rare, chronic, multisystem vasculitis that can involve arteries and veins of all sizes, with vascular manifestations representing some of its most severe and potentially life‐threatening complications. Arterial involvement is uncommon but clinically significant, particularly in young patients.
Alhareth M. Amro +5 more
wiley +1 more source
Undermined and Overlooked: A Diagnostic Challenge in the Gluteal Cleft
JEADV Clinical Practice, Volume 5, Issue 1, Page 330-332, March 2026.
G. E. Beraja, Y. Dalia, J. A. Jaller
wiley +1 more source
Case Reports in Gastrointestinal Medicine, Volume 2026, Issue 1, 2026.Background Myelodysplastic syndromes (MDSs) are clonal hematopoietic disorders often associated with cytogenetic abnormalities, among which trisomy 8 is one of the most common abnormalities. Trisomy 8 is linked to autoimmune manifestations, including Behçet‐like disease, especially with gastrointestinal involvement.
Zhan-Yue Niu +6 more
wiley +1 more source
International Journal of Dermatology, Volume 65, Issue 3, Page 600-602, March 2026.
Nana A. Fosu +7 more
wiley +1 more source
Kikuchi–Fujimoto Disease Presenting With Complex Neurological Manifestations: A Case Report
Case 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