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巨细胞动脉炎患者双眼复视的特征和预后。

Characteristics and Prognosis of Binocular Diplopia in Patients With Giant Cell Arteritis.

机构信息

Internal Medicine Department (TC, GC, TL), Neuro-Ophtalmology Department (MP, CV-C), and Neuroradiology Department (AL), Hopital Fondation Adolphe de Rothschild, Paris, France.

出版信息

J Neuroophthalmol. 2024 Mar 1;44(1):87-91. doi: 10.1097/WNO.0000000000001912. Epub 2023 Jun 21.

Abstract

BACKGROUND

Giant cell arteritis (GCA) is a large vessel vasculitis associated with a risk of permanent ophthalmologic complications. Data about diplopia prognosis in GCA are scarce. This study was designed to better characterize diplopia in newly diagnosed GCA patients.

METHODS

All consecutive patients diagnosed with GCA from January 2015 to April 2021 in a French tertiary ophthalmologic center were retrospectively reviewed. GCA diagnosis relied on a positive temporal artery biopsy or high-definition MRI.

RESULTS

Among 111 patients diagnosed with GCA, 30 patients (27%) had diplopia. Characteristics of patients with diplopia were similar to other GCA patients. Diplopia resolved spontaneously in 6 patients (20%). Diplopia was attributed to cranial nerve palsy in 21/24 patients (88%), especially third (46%) and sixth cranial nerve (42%). Ocular ischemic lesions occurred in 11 of the 30 patients with diplopia (37%); 2 patients developed vision loss after initiation of corticosteroids. In the remaining 13 patients, diplopia resolved after treatment onset in 12 patients (92%) with a median delay of 10 days. Patients treated intravenously tended to have a quicker improvement than those treated orally, but with a similar resolution rate of diplopia at 1 month. Two patients had relapse of diplopia at 4 and 6 weeks after an initial treatment course of 24 and 18 months, respectively.

CONCLUSIONS

Diplopia is a rare feature at GCA diagnosis, but should raise clinician suspicion for GCA when associated with cephalic symptoms and prompt the initiation of corticosteroids to prevent ocular ischemic complications.

摘要

背景

巨细胞动脉炎(GCA)是一种大血管血管炎,伴有永久性眼科并发症的风险。关于 GCA 复视预后的数据很少。本研究旨在更好地描述新诊断的 GCA 患者的复视情况。

方法

回顾性分析 2015 年 1 月至 2021 年 4 月在法国一家三级眼科中心诊断为 GCA 的所有连续患者。GCA 的诊断依赖于阳性颞动脉活检或高分辨率 MRI。

结果

在 111 例诊断为 GCA 的患者中,有 30 例(27%)有复视。有复视的患者特征与其他 GCA 患者相似。6 例(20%)患者的复视自发缓解。24 例复视患者中有 21 例(88%)归因于颅神经麻痹,特别是第三(46%)和第六颅神经(42%)。30 例有复视的患者中有 11 例(37%)发生眼缺血性病变;2 例患者在开始皮质类固醇治疗后出现视力丧失。在其余 13 例患者中,12 例(92%)患者在治疗开始后复视得到缓解,中位数延迟 10 天。静脉治疗的患者比口服治疗的患者改善更快,但在 1 个月时复视的缓解率相似。2 例患者在初始治疗 24 个月和 18 个月后分别出现 4 周和 6 周复视复发。

结论

复视是 GCA 诊断时罕见的特征,但当与头部症状相关时,应引起临床医生对 GCA 的怀疑,并促使开始皮质类固醇治疗,以预防眼缺血性并发症。

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