Casey Eye Institute, Oregon Health & Science University, Portland.
Department of Ophthalmology, Institute of Health Sciences, College of Medicine, Gyeongsang National University, Jinju, Gyeongnam 52727, South Korea.
JAMA Ophthalmol. 2018 Feb 1;136(2):109-115. doi: 10.1001/jamaophthalmol.2017.5466.
Idiopathic disease is the most frequent diagnosis in a uveitis clinic. The need to distinguish sarcoidosis from idiopathic uveitis is controversial. However, cardiac involvement in sarcoidosis can be life-threatening.
To report a series of patients with uveitis and cardiac sarcoidosis to illustrate the importance of categorizing the causes of uveitis.
DESIGN, SETTING, AND PARTICIPANTS: This retrospective observational case series reviewed the medical records of 249 patients with uveitis who were referred to the Casey Eye Institute between July 1, 2008, and February 28, 2017.
We describe patients who initially received a diagnosis of idiopathic uveitis but subsequently received a diagnosis of sarcoidosis. Clinical data, including ophthalmologic findings, were collected. We summarized the number of patients who initially presented with idiopathic uveitis, the number of patients who recived a classification of idiopathic uveitis after evaluation, the number of patients who underwent chest computed tomography or an electrocardiogram, and the number of patients with ocular sarcoidosis.
Of 33 patients with sarcoidosis, 21 (63.6%) were women and the mean (SD) age was 53.5 (13.8) years. Of 249 patients, the referring diagnosis was idiopathic uveitis for 179 (72%). After history, examination, and laboratory testing, 127 (51%) were still considered to have idiopathic disease. Fifty-three of the 179 patients (30%) with idiopathic disease underwent chest computed tomography scanning. A diagnosis of presumed sarcoidosis, usually on the basis of a chest computed tomography scan, was made in 19 patients (36.2%). As 14 patients (5.6%) were previously known to have sarcoidosis, 33 patients (13.3%) were evaluated with definite or presumed ocular sarcoidosis. We obtained electrocardiograms as a screen for cardiac sarcoidosis on 14 (42.4%) of these patients. Nine patients with abnormal electrocardiogram results were referred to cardiologists. Four of the 19 patients (21.1%) who were referred for idiopathic uveitis but subsequently received a diagnosis of presumed sarcoidosis were found to have episodes of ventricular tachycardia that required implantable cardiac defibrillators. Distinguishing ocular sarcoidosis from idiopathic uveitis had potentially life-saving implications for these patients.
The present case series shows the potential utility of distinguishing sarcoidosis-associated uveitis from idiopathic uveitis. We suggest that patients older than 40 years with a history of idiopathic uveitis be evaluated with chest computed tomography and an electrocardiogram if sarcoidosis is suggested on ophthalmic examination.
特发性疾病是葡萄膜炎门诊最常见的诊断。区分结节病和特发性葡萄膜炎的必要性存在争议。然而,结节病的心脏受累可能危及生命。
报告一系列患有葡萄膜炎和心脏结节病的患者,以阐明对葡萄膜炎病因进行分类的重要性。
设计、设置和参与者:这项回顾性观察性病例系列研究回顾了 2008 年 7 月 1 日至 2017 年 2 月 28 日期间向凯西眼科研究所转诊的 249 名葡萄膜炎患者的病历。
我们描述了最初被诊断为特发性葡萄膜炎但随后被诊断为结节病的患者。收集了包括眼科检查结果在内的临床数据。我们总结了最初表现为特发性葡萄膜炎的患者数量、经评估后被诊断为特发性葡萄膜炎的患者数量、接受胸部计算机断层扫描或心电图检查的患者数量以及患有眼部结节病的患者数量。
33 例结节病患者中,21 例(63.6%)为女性,平均(SD)年龄为 53.5(13.8)岁。在 249 名患者中,179 名(72%)的转诊诊断为特发性葡萄膜炎。经过病史、检查和实验室检查,仍有 127 名(51%)被认为患有特发性疾病。在 179 名患有特发性疾病的患者中,53 名(30%)接受了胸部计算机断层扫描。19 名患者(36.2%)根据胸部计算机断层扫描诊断为疑似结节病。作为 14 名(5.6%)先前已知患有结节病的患者,33 名(13.3%)接受了明确或疑似眼部结节病的评估。我们对其中 14 名(42.4%)患者进行了心电图检查,作为心脏结节病的筛查。9 名心电图异常结果的患者被转介给心脏病专家。在因特发性葡萄膜炎而被转介但随后被诊断为疑似结节病的 19 名患者中,有 4 名患者出现需要植入式心脏除颤器的室性心动过速发作。对这些患者来说,区分眼部结节病和特发性葡萄膜炎具有潜在的救生意义。
本病例系列表明,区分结节病相关葡萄膜炎与特发性葡萄膜炎具有潜在的实用性。我们建议,如果眼科检查提示结节病,年龄大于 40 岁且有特发性葡萄膜炎病史的患者应接受胸部计算机断层扫描和心电图检查。