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眼眶挛缩:韦格纳肉芽肿病患者炎症性眼眶疾病的一种并发症。

Orbital socket contracture: a complication of inflammatory orbital disease in patients with Wegener's granulomatosis.

作者信息

Talar-Williams C, Sneller M C, Langford C A, Smith J A, Cox T A, Robinson M R

机构信息

National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892, USA.

出版信息

Br J Ophthalmol. 2005 Apr;89(4):493-7. doi: 10.1136/bjo.2004.050039.

Abstract

AIM

To describe the clinical characteristics of orbital socket contracture in patients with Wegener's granulomatosis (WG).

METHODS

A retrospective cohort study The medical records of 256 patients with WG examined at the National Institutes of Health from 1967 to 2004 were reviewed to identify patients with orbital socket contracture. Details of the orbital disease including Hertel exophthalmometry readings, radiological findings, and results of eye examinations were recorded. Orbital socket contracture was defined as orbital inflammation with proptosis followed by the development of enophthalmos and radiographic evidence of residual fibrotic changes in the orbit. To examine for risk factors in the development of a contracted orbit, patients with orbital socket contracture were compared to patients without contracture with respect to multiple variables including history of orbital surgery, orbital disease severity, and major organ system involvement. The main outcome measures were the clinical characteristics of orbital socket contracture associated with inflammatory orbital disease in patients with WG.

RESULTS

Inflammatory orbital disease occurred in 34 of 256 (13%) patients and detailed clinical data on 18 patients were available and examined. Orbital socket contracture occurred during the clinical course in six patients; the features included restrictive ophthalmopathy (five), chronic orbital pain (three), and ischaemic optic nerve disease (two) resulting in blindness (no light perception) in one patient. The orbital socket contracture occurred within 3 months of treatment with immunosuppressive medications for inflammatory orbital disease in five patients and was not responsive to immunosuppressive medications. The median degree of enophthalmos in the contracted orbit compared with the fellow eye was 2.8 mm (range 1.5-3.5 mm) by Hertel exophthalmometry. There were no risk factors that predicted development of orbital socket contracture.

CONCLUSIONS

In six patients with WG and active inflammatory orbital disease, orbital socket contracture occurred during the treatment course with systemic immunosuppressive medications. The orbital socket contracture, presumably caused by orbital fibrosis, led to enophthalmos, restrictive ophthalmopathy, chronic orbital pain, and optic nerve disease and was not responsive to immunosuppressive therapy. Orbital socket contracture has not been previously reported as a complication of inflammatory orbital disease associated with WG and was an important cause of visual morbidity in our cohort of patients.

摘要

目的

描述韦格纳肉芽肿(WG)患者眼眶挛缩的临床特征。

方法

一项回顾性队列研究。对1967年至2004年在美国国立卫生研究院接受检查的256例WG患者的病历进行回顾,以确定眼眶挛缩患者。记录眼眶疾病的详细信息,包括赫特尔突眼计测量值、放射学检查结果和眼部检查结果。眼眶挛缩定义为伴有眼球突出的眼眶炎症,随后出现眼球内陷以及眼眶残留纤维化改变的影像学证据。为了研究眼眶挛缩发生的危险因素,将眼眶挛缩患者与无挛缩患者在多个变量方面进行比较,包括眼眶手术史、眼眶疾病严重程度和主要器官系统受累情况。主要观察指标为与WG患者炎症性眼眶疾病相关的眼眶挛缩的临床特征。

结果

256例患者中有34例(13%)发生炎症性眼眶疾病,18例患者有详细的临床资料并接受检查。6例患者在临床病程中出现眼眶挛缩;其特征包括限制性眼病(5例)、慢性眼眶疼痛(3例)和缺血性视神经疾病(2例),其中1例患者导致失明(无光感)。5例患者在使用免疫抑制药物治疗炎症性眼眶疾病后3个月内出现眼眶挛缩,且对免疫抑制药物无反应。通过赫特尔突眼计测量,挛缩眼眶与对侧眼相比,眼球内陷的中位程度为2.8 mm(范围1.5 - 3.5 mm)。没有预测眼眶挛缩发生的危险因素。

结论

在6例患有WG和活动性炎症性眼眶疾病的患者中,眼眶挛缩发生在全身免疫抑制药物治疗过程中。眼眶挛缩可能由眼眶纤维化引起,导致眼球内陷、限制性眼病、慢性眼眶疼痛和视神经疾病,且对免疫抑制治疗无反应。眼眶挛缩此前未被报道为与WG相关的炎症性眼眶疾病的并发症,是我们研究队列中导致视力损害的重要原因。

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