Transverse myelitis in a patient with Behcet’s disease: favorable outcome with a combination of interferon-α

2004 ◽  
Vol 24 (1) ◽  
pp. 64-66 ◽  
Author(s):  
Meral Çalgüneri ◽  
Ahmet Mesut Onat ◽  
M. Akif Öztürk ◽  
Levent Özçakar ◽  
Kemal Ureten ◽  
...  
2012 ◽  
Vol 19 (1) ◽  
pp. 39
Author(s):  
Han-Jun Bae ◽  
Chang Gyu Jung ◽  
Ju Hyung Lee ◽  
Tae Yul Kim ◽  
Sunyoung Lee ◽  
...  

2010 ◽  
Vol 62 (9) ◽  
pp. 2796-2805 ◽  
Author(s):  
Christoph M. E. Deuter ◽  
Manfred Zierhut ◽  
Antje Möhle ◽  
Reinhard Vonthein ◽  
Nicole Stöbiger ◽  
...  

2007 ◽  
Vol 30 (3) ◽  
pp. 294-296 ◽  
Author(s):  
Levent Sinan Bir ◽  
Fatma Özdemir Eşmeli ◽  
Utku Cenikli ◽  
×ağdaş Erdoğan ◽  
Eylem Değirmenci

2009 ◽  
Vol 75 (6) ◽  
pp. 720-722 ◽  
Author(s):  
Paola Pivetti-Pezzi ◽  
Massimo Accorinti ◽  
Maria Pia Pirraglia ◽  
Roberta Priori ◽  
Guido Valesini

2015 ◽  
Vol 22 (7) ◽  
pp. 960-963 ◽  
Author(s):  
Hyung Seok Lee ◽  
Do Young Kim ◽  
Ha Young Shin ◽  
Young-Chul Choi ◽  
Seung Min Kim

Background: Spinal cord involvement in Behçet’s disease is not well studied. Objective: To evaluate the clinical, laboratory and magnetic resonance imaging characteristics of spinal cord involvement in Behçet’s disease. Methods: We retrospectively reviewed 10 spinal cord involvements in seven patients with Behçet’s disease. Results: The median age of onset for spinal cord involvement was 32 (23–45 years). Two patients showed a secondary progressive course. Cerebrospinal fluid findings revealed mild to moderate pleocytosis and/or elevated protein levels. In eight spinal cord involvements, the lesion was longer than three vertebrae. Serum anti-aquaporin-4 antibody was negative in all four patients tested. Conclusions: Longitudinally extensive transverse myelitis is a characteristic manifestation of spinal cord involvement in Behçet’s disease.


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