Ocular features of Behcet's disease: An international collaborative study

被引:140
作者
Kitaichi, Nobuyoshi [1 ]
Miyazaki, Akiko
Stanford, Miles R.
Chams, Hormoz
Iwata, Daiju
Ohno, Shigeaki
机构
[1] Hokkaido Univ, Grad Sch Med, Dept Ophthalmol & Visual Sci, Sapporo, Hokkaido 0608638, Japan
[2] St Thomas Hosp, Med Eye Unit, London, England
[3] Univ Tehran, Shariati Hosp, Behcets Res Ctr, Tehran 14174, Iran
关键词
D O I
10.1136/bjo.2007.123554
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objective: To investigate the clinical features of ocular lesions in Behcet's disease in different countries. Methods: A descriptive questionnaire survey was performed. Results: 25 eye centres in 14 countries returned questionnaires on prevalent cases in 2006. Clinical data were analysed on 1,465 patients with ocular lesions. Recurrent oral aphthous ulcers were reported in 94.5%, skin lesions in 69.5% and genital ulcers in 61.4%. Most of the patients had bilateral and recurrent intraocular inflammation. Poor visual acuity was seen in 18.9% in women, but 24.8% in men (p<0.01). Panuveitis was seen more in men than in women (p<0.01). 23% of the patients had visual acuity equal to or worse than 20/200 at the final visit. The patients with poor vision were more frequently in India, Iran and Japan than in other countries (p<0.01). Conclusions: We report the largest contemporary international case series of patients with ocular involvement in Behcet's disease. Panuveitis was significantly more frequent in men than women, and men tended to have a worse visual prognosis. There were some differences in the clinical pattern of Behcet's disease in different countries. Despite modern treatment, the disease still carries a poor visual prognosis with one-quarter of the patients blind.
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收藏
页码:1579 / 1582
页数:4
相关论文
共 22 条
[1]   Statistical analysis of endogenous uveitis at Tokyo University Hospital (1998-2000) [J].
Akiyama, K ;
Numaga, J ;
Yoshida, A ;
Kawashima, H ;
Kaburaki, T ;
Fujino, Y .
JAPANESE JOURNAL OF OPHTHALMOLOGY, 2006, 50 (01) :69-71
[2]   Behcet's disease: Clinical study of Jordanian patients [J].
AlAboosi, MA ;
Salem, MA ;
Saadeh, A ;
AlJamal, M ;
Hijawi, M ;
Khammash, M ;
Sharma, RV .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1996, 35 (09) :623-625
[3]   FUNDUS CHANGES ASSOCIATED WITH BEHCETS-DISEASE [J].
ATMACA, LS .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 1989, 227 (04) :340-344
[4]   Prevalence of Behcet's disease in Istanbul, Turkey [J].
Azizlerli, G ;
Köse, AA ;
Sarica, R ;
Gül, A ;
Tutkun, IT ;
Kulaç, M ;
Tunç, R ;
Urgancioglu, M ;
Disçi, R .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 2003, 42 (10) :803-806
[5]   Efficacy of interferon alpha in the treatment of refractory and sight threatening uveitis: a retrospective monocentric study of 45 patients [J].
Bodaghi, Bahram ;
Gendron, Gael ;
Wechsler, Bertrand ;
Terrada, Celine ;
Cassoux, Nathalie ;
Huong, Du Le Thi ;
Lemaitre, Claire ;
Fradeau, Christine ;
LeHoang, Phuc ;
Piette, Jean-Charles .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2007, 91 (03) :335-339
[6]   Behcet's disease in Lebanon: clinical profile, severity and two-decade comparison [J].
Hamdan, A ;
Mansour, W ;
Uthman, I ;
Masri, AF ;
Nasr, F ;
Arayssi, T .
CLINICAL RHEUMATOLOGY, 2006, 25 (03) :364-367
[7]  
Krause I, 2001, J RHEUMATOL, V28, P1033
[8]   The long-term mortality and morbidity of Behcet syndrome - A 2-decade outcome survey of 387 patients followed at a dedicated center [J].
Kural-Seyahi, E ;
Fresko, I ;
Seyahi, N ;
Ozyazgan, Y ;
Mat, C ;
Hamuryudan, V ;
Yurdakul, S ;
Yazici, H .
MEDICINE, 2003, 82 (01) :60-76
[9]  
MIZUSHIMA Y, 1988, INT J TISSUE REACT, V10, P59
[10]  
MOUSA ARA, 1986, SCAND J RHEUMATOL, V15, P310