Department of Ophthalmology and Neuroscience, University of Bari "Aldo Moro", Medical School, Bari, Italy.
Department of Uveitis and Ocular Pathology, Sankara Nethralaya, Chennai, India.
Int Ophthalmol. 2020 Dec;40(12):3453-3467. doi: 10.1007/s10792-020-01531-0. Epub 2020 Aug 1.
To describe the ocular manifestations in a cohort of patients with systemic sarcoidosis (SS). Recent advances in the pathophysiology, diagnosis, and therapy of SS are also discussed.
Data from 115 Italian patients diagnosed between 2005 and 2016 were retrospectively reviewed. All but the first 17 patients underwent a comprehensive ophthalmologic examination. The diagnosis was based on clinical features, the demonstration of non-caseating granulomas in biopsies from involved organs, and multiple imaging techniques. Data on broncho-alveolar lavage fluid analysis, calcemia, calciuria, serum angiotensin-converting enzyme levels and soluble interleukin-2 receptor levels were retrieved when available.
Ocular involvement, detected in 33 patients (28.7%), was bilateral in 29 (87.9%) and the presenting feature in 13 (39.4%). Anterior uveitis was diagnosed in 12 patients (36.4%), Löfgren syndrome and uveoparotid fever in one patient each (3%), intermediate uveitis in 3 patients (9.1%), posterior uveitis in 7 (21.2%), and panuveitis in 9 (27.3%). First-line therapy consisted of corticosteroids, administered as eyedrops (10 patients), sub-Tenon's injections (1 patient), intravitreal implants (9 patients), or systemically (23 patients). Second-line therapy consisted of steroid-sparing immunosuppressants, including methotrexate (10 patients) and azathioprine (10 patients). Based on pathogenetic indications that tumor necrosis factor (TNF)-α is a central mediator of granuloma formation, adalimumab, targeting TNF-α, was employed in 6 patients as a third-line agent for severe/refractory chronic sarcoidosis.
Uveitis of protean type, onset, duration, and course remains the most frequent ocular manifestation of SS. Diagnostic and therapeutic advancements have remarkably improved the overall visual prognosis. An ophthalmologist should be a constant component in the multidisciplinary approach to the treatment of this often challenging but intriguing disease.
描述一组系统性结节病(SS)患者的眼部表现。还讨论了 SS 的发病机制、诊断和治疗的最新进展。
回顾性分析了 2005 年至 2016 年间诊断的 115 名意大利患者的数据。除前 17 名患者外,所有患者均接受了全面的眼科检查。诊断基于临床特征、受累器官活检中无干酪样肉芽肿的证明以及多种影像学技术。如果有数据,则检索支气管肺泡灌洗液分析、血钙、钙尿、血清血管紧张素转换酶水平和可溶性白细胞介素-2 受体水平的数据。
33 名(28.7%)患者存在眼部受累,29 名(87.9%)为双侧,13 名(39.4%)为首发症状。12 名(36.4%)患者诊断为前葡萄膜炎,1 名(3%)患者分别诊断为 Löfgren 综合征和葡萄膜唾液腺热,3 名(9.1%)患者诊断为中间葡萄膜炎,7 名(21.2%)患者诊断为后葡萄膜炎,9 名(27.3%)患者诊断为全葡萄膜炎。一线治疗包括皮质类固醇,包括滴眼剂(10 例)、Tenon 下注射(1 例)、玻璃体内植入物(9 例)或全身(23 例)。二线治疗包括皮质类固醇保留免疫抑制剂,包括甲氨蝶呤(10 例)和硫唑嘌呤(10 例)。根据肿瘤坏死因子(TNF)-α是肉芽肿形成的中心介质的发病机制,针对 TNF-α 的阿达木单抗被用作 6 例严重/难治性慢性结节病的三线药物。
多形性、发病、持续时间和病程的葡萄膜炎仍然是 SS 最常见的眼部表现。诊断和治疗的进步极大地改善了整体视觉预后。眼科医生应该成为治疗这种经常具有挑战性但又引人入胜的疾病的多学科方法的固定组成部分。