Results 61 to 70 of about 1,422 (110)

Exploring the Vasculitis‐Tumors Link: Epidemiological Patterns, Mechanistic Insights, and Clinical Implications

Advanced Science, Volume 13, Issue 14, 9 March 2026.
This review outlines association between vasculitis and malignancies and provides practical value for clinicians in distinguishing primary vasculitis from malignancy‐associated forms and optimizing patient surveillance, improving recognition of tumor‐associated vasculitis to reduce the risk of misdiagnosis, supporting more accurate clinical decision ...
Xiaofei Shi, Zhijiao Li, Xin Ma, Bei Zhang, Xinfeng Wu, Hua Fan, Rongzeng Liu, Hongwei Jiang, Cong‐Qiu Chu   +8 more
wiley   +1 more source

MEFV Gene Mutations in Behçet’s Disease

Eurasian Journal of Medicine, 2019
Behçet's disease is a chronic inflammatory multisystemic disorder of unknown cause, characterized by orogenital ulcers, uveitis, skin lesions, vascular, locomotor, pulmoner, gastrointestinal, and central nervous system manifestations.
Fazile Hatipoğlu Erdem
doaj  

Persistent fever, neck swelling, and small vessel vasculitis following tonsillectomy in a patient with Behçet’s disease: a case report

Journal of Medical Case Reports, 2012
Introduction Behçet’s disease commonly presents with recurrent oral and genital mucocutaneous ulcerations, uveitis and various skin manifestations. Other clinical symptoms include gastrointestinal ulcerations, arthritis, venous thrombosis, arterial ...
Wagner Claudia, Schär Dominik, Tinguely Marianne, Kunz Isabelle   +3 more
doaj   +1 more source

Decreasing Serum Adropin Levels in Patients With Systemic Lupus Erythematosus: A Case‐Control Study

Health Science Reports, Volume 9, Issue 3, March 2026.
ABSTRACT Introduction Systematic lupus erythematosus is a complex fundamental autoimmune disease with relapsing‐remitting course and spectrum of disease ranging from mild to life‐threatening illness. Approximately half of women diagnosed with systemic lupus erythematosus (SLE) are affected by obesity, with rates reaching up to 50%.
Mehrzad Hajialilo, Amir Ghorbanihaghjo, Kamran Javidi‐Aghdam, Seyed Amir Hossein Seyeddorraji, Alireza Khabbazi, Mehdi Jafarpour   +5 more
wiley   +1 more source

Vision-Threatening Behcet’s Disease: Severity of Ocular Involvement Predictors

Journal of Ophthalmology, 2018
Purpose. To examine and spot systemic findings commonly associated with a serious form of ocular Behcet’s disease. This could potentially help ophthalmologists categorize their patients based on future risk and plan treatment accordingly.
Mohammed A. Hussein, Iman M. Eissa, Ahmed A. Dahab   +2 more
doaj   +1 more source

Dupilumab Treatment in Pemphigus: A Report of Three Cases and Literature Review

JEADV Clinical Practice, Volume 5, Issue 1, Page 254-257, March 2026.
Capsule summary Pemphigus vulgaris and foliaceus are rare autoimmune blistering diseases traditionally treated with corticosteroids, immunosuppressants, intravenous immunoglobulins, and rituximab. A subset of patients remains refractory or has contraindications to these conventional therapies. We present three cases of pemphigus treated with dupilumab.
José Javier Mateos Rico, Marta Gutiérrez Pascual, María Dolores Caro Gutiérrez, Cristina Marcos Rodríguez, Javier de Quadros Malagón, Francisco Javier Vicente Martín   +5 more
wiley   +1 more source

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

Respirology Case Reports
Behcet'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, Naveen Polavarapu, Jithin Mathew, Virender Pratibh Prasad, Venkata Nagarjuna Maturu   +4 more
doaj   +1 more source

Behcet's disease and associations with HLA-B5 antigen (a review of literature and the authors' findings)

Терапевтический архив, 2010
Aim. To estimate the distribution of HLA Class I (A, B) antigens in patients with Behcet's disease (BD) and the association of HLA-B5 antigen with the clinical manifestations of the disease in different ethnic and population groups in relation to gender.
Regina Georgievna Goloeva, Zemfira Sadullaevna Alekberova, Irina Anatol'evna Guseva, Mikhail Yur'evich Krylov, R G Goloyeva, Z S Alekberova, I A Guseva, M Yu Krylov   +7 more
doaj  

Neurological Behcet’s disease with transverse myelitis in an adolescent: A case report

SAGE Open Medical Case Reports
Neurological Behcet’s disease is a rare systemic vasculitis marked by recurrent oral or genital ulcers, eye manifestations of uveitis or retinal vasculitis, and skin lesions.
Jeanine McColl, Teresa Liang, Dax G. Rumsey   +2 more
doaj   +1 more source

Antistreptolysin O Levels in Patients with Behcet’s Disease

Eurasian Journal of Medicine, 2011
Objective: Behcet’s disease is a multisystem inflammatory disorder, and its etiology has not been defined clearly yet. In this study, we aimed to investigate the antistreptolysin O (ASO) levels of patients with Behcet’s disease.
Hulya Uzkeser, Saliha Karatay, Kadir Yildirim, Ali Karakuzu, Muhammed Hamidullah Uyanik   +4 more
doaj