Zulfiqar Abrar-Ahmad
Department of Internal Medicine, University Hospital of Strasbourg, 1 porte de l'hôpital, 67000 Strasbourg, France.
Caspian J Intern Med. 2022 Summer;13(3):642-645. doi: 10.22088/cjim.13.3.642.
Giant cell arteritis (GCA) is a vasculitis of the large and medium-sized arteries in the elderly whose ischemic complications adversely affect the eye. The irreversible loss of visual acuity is most often related to acute anterior ischemic optic neuropathy. Very few cases of scleritis have been described in the literature.
The patient presented an obvious case of giant cell arteritis, initially revealed by an ophthalmologic involvement in the form of posterior scleritis, an ear, nose, and throat (ENT) involvement with vestibular and neurological involvement with a type of peripheral neuropathy, all evolving in the context of a weight loss of 8 kg and a marked biological inflammatory syndrome. The patient presented several relapses of giant cell arteritis in the form of several episodes of anterior and posterior, right and left, and even bilateral, isolated scleritis without any other clinical or biological abnormalities, always in conjunction with a decrease in corticosteroid therapy. In the presence of corticosteroid dependence and resistance to methotrexate, tocilizumab was initiated.
The therapeutic management of scleritis associated with giant cell arteritis is difficult. In the absence of a codified scheme, the treatment remains empirical, based on the experience of the various teams. In this context, biotherapies (anti-IL6 type, such as tocilizumab) are increasingly used.
巨细胞动脉炎(GCA)是一种发生于老年人的大中动脉血管炎,其缺血性并发症会对眼睛产生不利影响。视力不可逆丧失最常与急性前部缺血性视神经病变有关。文献中描述的巩膜炎病例极少。
该患者表现为典型的巨细胞动脉炎,最初表现为眼科方面的后部巩膜炎,耳鼻喉科方面的前庭受累以及伴有某种周围神经病变类型的神经受累,所有这些情况都在体重减轻8千克和明显的生物炎症综合征背景下发生。患者出现了几次巨细胞动脉炎复发,表现为多次前部和后部、右侧和左侧甚至双侧的孤立性巩膜炎发作,且无任何其他临床或生物学异常,每次发作均与皮质类固醇治疗减量有关。在存在皮质类固醇依赖且对甲氨蝶呤耐药的情况下,开始使用托珠单抗治疗。
巨细胞动脉炎相关巩膜炎的治疗管理具有挑战性。由于缺乏规范方案,治疗仍基于各团队的经验,具有一定的经验性。在此背景下,生物疗法(如抗IL-6类,如托珠单抗)的使用越来越多。