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印度人群中的白塞病谱系

Spectrum of Behçet's disease in the Indian population.

作者信息

Sachdev Nishant, Kapali Nandhini, Singh Ramandeep, Gupta Vishali, Gupta Amod

机构信息

Department of Ophthalmology, Post Graduate Institute of Medical Education and Research, Sector 12, Chandigarh, 160012, India.

出版信息

Int Ophthalmol. 2009 Dec;29(6):495-501. doi: 10.1007/s10792-008-9273-8. Epub 2008 Oct 21.

Abstract

The purpose of this investigation is to study the clinical profile of Behçet's disease in the Indian population as seen in a tertiary referral uveitis clinic. A retrospective non-comparative case series was used. The records of all of the patients seen in our uveitis clinic between January 1990 and December 2006 were screened and patients with a diagnosis of Behçet's disease were enrolled. The diagnosis was based on the Japanese diagnostic criteria and patients were classified into complete, incomplete, suspected, and possible Behçet's disease. Information on the patient's demographic characteristics, ocular and systemic clinical features, complications, investigation results, management protocols, and visual outcome was collected. The records of 4,214 uveitis clinic patients were screened and 53 patients (1.25%) of Behçet's disease were identified. These included 39 males and 14 females (2.8:1), with a mean age of 27.6 years (range 10-51 years). Fifty (94.3%) of these patients were of either complete or incomplete Behçet's disease. Ocular involvement was the most common manifestation (49 patients, 92.4%), followed by oral ulcers (88.7%), genital ulcers (61.2%), and skin involvement (28.3%). Panuveitis (57.1%) was the most common ocular presentation, followed by posterior (26.5%) and anterior uveitis (16.3%). More than 95% of the patients required oral steroids, while additional immunosuppressants were used in nearly 53% of the patients. The common complications observed included complicated cataract (57% of eyes), followed by cystoid macular edema (55.1%), occlusive vasculitis (44.8%), and optic atrophy (26.5%). Nearly 36% of the eyes maintained 6/12 or better vision, while 38% of the eyes were less than 6/60 after a mean follow-up period of 4.9 years (range 2-16 years). Behçet's disease, although rare among Indians, commonly manifests with ocular involvement as non-granulomatous panuveitis with a high incidence of complications and unfavorable visual outcome in nearly one-third of the cases.

摘要

本研究的目的是在一家三级转诊葡萄膜炎诊所中,研究印度人群中白塞病的临床特征。采用回顾性非对照病例系列研究。筛查了1990年1月至2006年12月期间在我们葡萄膜炎诊所就诊的所有患者的记录,并纳入了诊断为白塞病的患者。诊断基于日本诊断标准,患者被分为完全型、不完全型、疑似和可能的白塞病。收集了患者的人口统计学特征、眼部和全身临床特征、并发症、检查结果、治疗方案及视力预后等信息。筛查了4214例葡萄膜炎诊所患者的记录,确诊53例(1.25%)白塞病患者。其中男性39例,女性14例(2.8:1),平均年龄27.6岁(范围10 - 51岁)。这些患者中有50例(94.3%)为完全型或不完全型白塞病。眼部受累是最常见的表现(49例,92.4%),其次是口腔溃疡(88.7%)、生殖器溃疡(61.2%)和皮肤受累(28.3%)。全葡萄膜炎(57.1%)是最常见的眼部表现,其次是后葡萄膜炎(26.5%)和前葡萄膜炎(16.3%)。超过95%的患者需要口服类固醇,近53%的患者使用了其他免疫抑制剂。观察到的常见并发症包括复杂性白内障(57%的眼),其次是黄斑囊样水肿(55.1%)、闭塞性血管炎(44.8%)和视神经萎缩(26.5%)。平均随访4.9年(范围2 - 16年)后,近36%的眼视力维持在6/12或更好,而38%的眼视力低于6/60。白塞病在印度人中虽然罕见,但通常表现为眼部受累,以非肉芽肿性全葡萄膜炎为主,并发症发生率高,近三分之一的病例视力预后不佳。

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