نتایج جستجو برای: behcet syndrome

تعداد نتایج: 622147  

2015
Mithun Cherakara Mohan Jassim Mohhamed Koya Gopinath Vadakkupatty Palaniyandi Kandaswamy Venmadathayil Abdul Jaleel Parammal Ambadi Jimnaz Sreerag Manjuhasan Vinod Ravindran

Behcet's disease (BD) is characterized by recurrent oral and genital ulcers and uveitis. It is also known to affect various organs; however, central nervous system involvement is rare and may cause parenchymal or vascular lesions with distinct clinical syndromes. Various viral encephalitides are important differential diagnoses. MRI may aid the correct diagnosis. This case report describes a pa...

Journal: :Chest 2001
H Satoh H Ishikawa Y T Yamashita M Ohtsuka K Sekizawa

1 Mogulkoc N, Burgess MI, Bishop PW. Intracardiac thrombus in Behcet’s disease: a systematic review. Chest 2000; 118: 479–487 2 Ahn JM, Im JG, Ryoo JW, et al. Thoracic manifestations of Behcet syndrome: radiographic and CT findings in nine patients. Radiology 1995; 194:199–203 3 Imai H, Sakakibara M, Yoshida K, et al. Magnetic resonance imaging of cardiovascular thrombi [in Japanese]. J Cardiog...

2018
Ji Hwan Lee Christopher Seungkyu Lee Sung Chul Lee

BACKGROUND To evaluate therapeutic outcomes of interferon alpha-2a (IFNα2a) treatment in patients with Behcet's disease who were refractory to immunosuppressive agents. METHODS This retrospective case series reviewed the medical records of 5 patients with refractory Behcet uveitis from January 2011 to February 2017. IFNα2a was administered at a dose of 3 million IU 3 times per week. Clinical ...

2016
Ze-yang Ding Guan-nan Jin Xi Ai Li-yan Li Ping Zheng Yan Guan Qi Wang Zhi-wei Zhang Jun Yang

Aneurysm or pseudoaneurysm formation is one of the vascular complications of Behcet disease. At present, the optimal treatment for the disease has not been established.The authors report a case of vasculo-Behcet disease (v-BD) with recurrent pseudoaneurysms in the left infrainguinal arteries (common femoral artery, superficial femoral artery, and popliteal artery), as well as thrombosis in the ...

2013
Y Shinar G Breuer A Livneh P Hashkes

Case Report We confirmed the Muckle-Wells syndrome phenotype of CAPS by NLRP3 genetic testing in a three generation family of Turkish Jewish origin, previously diagnosed with familial Behcet disease due to the presence of mucosal ulcers in several family members with the finding of the HLA-B51 antigen in at least one family member. Eight family members including a deceased grandfather, 4 of his...

Journal: :European journal of medical and health sciences 2022

Purpose: To determine the rate of incidence and most common type macular complications in patients with Behcet disease. Methods: In this monocentric retrospective clinical study we examined all diagnosed disease between April 2018 2022 (150 patients). Each individual would undergo a complete ophthalmological examination, fundus retinography, OCT scan fluorescein angiography. Results: 54 150 pre...

Journal: :Korean Journal of Medicine 2013

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