Results 41 to 50 of about 2,477 (110)

Delayed Massive Haemoptysis Following EBUS‐TBNA Revealing a Pseudoaneurysm of an Ectopic Bronchial Artery: A Rare Complication at the Crossroads of Interventional Pulmonology and Radiology

Respirology Case Reports, Volume 13, Issue 12, December 2025.
A 31‐year‐old woman with Budd–Chiari syndrome developed delayed massive haemoptysis 1 week after EBUS‐TBNA due to pseudoaneurysms arising from 4R lymph nodes. Diagnosis was confirmed by CT angiography and bronchoscopy, and successful microcoil embolisation achieved complete resolution.
Julien G. Cohen, Matthieu Papillard, Romain Messe   +2 more
wiley   +1 more source

Human leukocyte antigen-associated uveitis in Thai population: Brief review

Journal of Associated Medical Sciences, 2015
Human Leukocyte Antigen (HLA) has been associated with several immune-mediated diseases, malignancies and infectious diseases. Due to the HLA complexity and polymorphisms, several types of HLA have been used as the molecular markers in diagnosis.
Nampeung Anukul, Nipapan Leetrakool, Kessara Pathanapitoon   +2 more
doaj  

Bilateral Retrobulbar Optic Neuritis as the First Manifestation of Neuro-Behçet Disease

Case Reports in Rheumatology, 2020
Background. Behçet disease (BD) is a polygenic and chronic autoinflammatory multisystem vasculitis. Acute optic neuritis has been rarely reported in patients with BD, especially in children. Case Presentation. We reported an 8-year-old girl with a sudden
Mohsen Jari, Taiiebeh Mohammadi, Ensiyeh Taheri   +2 more
doaj   +1 more source

Associations between HLA Class I alleles and the prevalence of nasopharyngeal carcinoma (NPC) among Tunisians

Journal of Translational Medicine, 2007
The high prevalence of nasopharyngeal cancer (NPC) in Southern Asia and Mediterranean Northern Africa suggests genetic predisposition among other factors.
Stroncek David, Bouaouina Noureddine, Selleri Silvia, Monaco Alessandro, Wang Ena, Robbins Fu-Meei, Chen Deborah, Adams Sharon, Piancatelli Daniela, Ghandri Nahla, Li Xin, Adorno Domenico, Chouchane Lotfi, Marincola Francesco M   +13 more
doaj   +1 more source

Long-Term Outcomes of Behçet’s Syndrome-Related Uveitis: A Monocentric Italian Experience

Mediators of Inflammation, 2020
Objectives. To examine demographic and clinical characteristics and long-term visual outcome in a cohort of Italian patients affected by Behçet’s uveitis (BU). Materials and Methods.
Jurgen Sota, Luca Cantarini, Antonio Vitale, Arianna Sgheri, Stefano Gentileschi, Valeria Caggiano, Viviana Gelardi, Bruno Frediani, Gian Marco Tosi, Claudia Fabiani   +9 more
doaj   +1 more source

Unraveling the Clinical and Molecular Landscape of Myocardial Infarction in Behçet's Syndrome: A Comprehensive Analysis

Immunity, Inflammation and Disease, Volume 13, Issue 11, November 2025.
ABSTRACT Objectives Behçet's syndrome (BS) is a rare inflammatory disorder with life‐threatening complications like myocardial infarction (MI), driven by vasculitis and immune‐mediated thrombosis. This study unveils distinct clinical and molecular profiles in BS patients with MI, employing gene analysis and Weighted Gene Co‐expression Network Analysis (
Li‐Yang Zhang, Chun‐Hui She, Hu Dan, Jun Zou, Jian‐Long Guan   +4 more
wiley   +1 more source

Interdisciplinary Approaches to Diagnostic Analysis in Behcet’s Disease

Journal of Indian Academy of Oral Medicine and Radiology
The exploration of Behçet’s disease challenges the idea that “the oral cavity reflects systemic diseases.” This chronic systemic vasculitis, characterized by oral and genital ulcers, cutaneous lesions, and multi-organ involvement, poses diagnostic ...
Arun Dev Sharma, Ajay Parihar, Sujata Tosh, Nidhi Yadav   +3 more
doaj   +1 more source

Changes in the proportion of clinical clusters contribute to the phenotypic evolution of Behçet’s disease in Japan

Arthritis Research & Therapy, 2021
Background We hypothesized that Behçet’s disease (BD) consists of several clinical subtypes with different severity, resulting in heterogeneity of the disease. Here, we conducted a study to identify clinical clusters of BD.
Yutaro Soejima, Yohei Kirino, Mitsuhiro Takeno, Michiko Kurosawa, Masaki Takeuchi, Ryusuke Yoshimi, Yumiko Sugiyama, Shigeru Ohno, Yukiko Asami, Akiko Sekiguchi, Toshihisa Igarashi, Shohei Nagaoka, Yoshiaki Ishigatsubo, Hideaki Nakajima, Nobuhisa Mizuki   +14 more
doaj   +1 more source

Rare Wound: Extensive Skin Lesions and Poor Wound Healing of the Calf in a Patient With Behçet's Disease

International Wound Journal, Volume 23, Issue 2, February 2026.
Xian Sun, Yang Xia, Jia‐Jun Wu, Ke‐Jia Li   +3 more
wiley   +1 more source

Roflumilast for Oral Ulcers in Behçet's Disease and Recurrent Aphthous Stomatitis

The Journal of Dermatology, Volume 52, Issue 11, Page 1713-1717, November 2025.
ABSTRACT Oral aphthous ulcer in Behçet's disease (BD) and recurrent aphthous stomatitis (RAS) is a cause of discomfort for many patients, especially in cases refractory to colchicine or azathioprine. Roflumilast, a phosphodiesterase‐4 (PDE4) inhibitor, may be effective for treating refractory oral ulcers (OUs) in BD and RAS, especially in regions where
Kyung Bae Chung, Hae June Sung, Eun Hye Kim, Hyunwoo Jang, Do‐Young Kim   +4 more
wiley   +1 more source