Results 11 to 20 of about 1,239,123 (172)

Low Level Laser Therapy to Reduce Recurrent Oral Ulcers in Behçet’s Disease

Case Reports in Dentistry, 2016
Behçet’s disease (BD) is a chronic, relapsing multisystemic vascular condition. Behçet’s disease was described by Hulusi Behçet in 1937. This rare multisystem relapsing-remitting inflammatory disease is poorly understood but is thought to be an ...
D. B. Gandhi Babu, Sunanda Chavva, Shefali Waghray, Neeharika Satya Jyothi Allam, Marella Kondaiah   +4 more
doaj   +2 more sources

Behçet’s Syndrome and Peri-emergence Trismus: A Case of Inflammatory Airway Compromise

Journal of Onco-Anaesthesiology and Perioperative Medicine
Behçet’s syndrome (BS) is a multisystemic autoimmune disorder characterised by recurrent oral and genital ulcers, uveitis and vasculitis. While its anaesthetic implications are well-documented, a rare and critical perioperative complication is acute ...
J. Rajitha, Suparna Mitra Barman, Jyotsna Goswami   +2 more
doaj   +2 more sources

Behçet’s Disease and Intracardiac Thrombosis: A Report of Three Cases [PDF]

Case Reports in Rheumatology, 2013
We present three patients with Behçet’s disease associated with intracardiac thrombus and pulmonary vascular involvement. One of these patients had also Budd-Chiari syndrome.
Nurşen Düzgün, Orhan Küçükşahin, Kayhan Çetin Atasoy, Canan Togay Işıkay, Demet Menekşe Gerede, Ayşe Erden, Seda Kaynak Şahap, Muhammed Arif İbiş, Aşkın Ateş   +8 more
doaj   +2 more sources

Behçet’s Disease and Neuro-Behçet’s Syndrome [PDF]

European Medical Journal Neurology, 2018
Behçet’s disease is an idiopathic chronic relapsing multisystem vascular-inflammatory disease of unknown origin, which usually presents with orogenital ulceration and uveitis and is identified as the triple-symptom complex.
Ugur Uygunoglu, Sabahattin Saip, Aksel Siva   +2 more
doaj   +1 more source

Millard–Gubler Syndrome due to Parenchymal Neuro-Behcet’s Syndrome Lesion: A Rare Case Report

Acta Neurologica Taiwanica
Behcet's disease; it is a vascular-inflammatory chronic recurrent disease that can affect many systems in the body. Millard–Gubler syndrome is one of the brainstem syndromes that occur due to lesions involving the ventral part of the caudal pons.
Bünyamin Tosunoğlu, Burcu Gökçe Çokal, Hafize Nalan Güneş, Tahir Kurtuluş Yoldaş   +3 more
doaj   +2 more sources

Nasal and Sinonasal Findings in Behçet's Syndrome: A Scoping Review. [PDF]

J Clin Med
Background: Nasal and sinonasal findings have been reported in patients with Behçet’s syndrome, but their frequency, clinical significance, and relationship to underlying disease remain unclear.
Otsuka Y, Masuda Y, Nishimura Y, Katayama Y, Otsuka F.   +4 more
europepmc   +2 more sources

Medication adherence in Behçet's syndrome: real-world data from a tertiary referral cohort. [PDF]

RMD Open
Objectives Medication adherence is a key determinant of treatment effectiveness in chronic inflammatory diseases but data in Behçet’s syndrome (BS) remain limited.
Talarico R, Di Cianni F, Sulis A, Lubrano Lavadera G, Marinello D, Mosca M.   +5 more
europepmc   +2 more sources

Behçet’s syndrome: recent advances to aid diagnosis

, 2023
Behçet’s syndrome is a recurring inflammatory multiorgan disorder affecting the skin, mucosa, eyes, joints, stomach, and central nervous system. Behçet’s syndrome epidemiology varies greatly among populations (0.64–420/100,000), and Behçet’s syndrome has
Brown, Kelly L., Balci-Peynircioglu, Banu, EKİCİ, MUSTAFA, AKBABA, TAYFUN HİLMİ, Çolpak, Ayşe İlksen, KARADAĞ, ÖMER   +5 more
core   +1 more source

Neutrophil and lymphocyte responses to oral Streptococcus in Adamantiades-Behcet's disease [PDF]

, 2005
Immune reactions against microorganisms play an important pathogenic role in Adamantiades-Behçet’s disease (ABD). We had previously obtained Streptococcus sanguinis (strain BD113-20) isolated from the oral cavity of patients with ABD.
Oguma, Keiji, Isogai, Emiko, Kurauchi, Tomomi, Fujinami, Yoshihito, Matsuo, Toshihiko, Yokota, Kenji, Isogai, Hiroshi, Ohtsuki, Hiroshi   +7 more
core   +1 more source

Budd-Chiari syndrome in a 25-year-old woman with Behçet's disease: a case report and review of the literature

Journal of Medical Case Reports, 2011
Introduction The risk that patients with Behçet's disease will develop thrombotic complications has been previously described. Although it is distributed worldwide, Behçet's disease is rare in the Americas and Europe.
Évora Paulo RB, Matsuda Nilce M, Oikawa Fernando T, Carvalho Daniela T, Yamada Alice T   +4 more
doaj   +1 more source