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Low dose corticosteroid in association with methotrexate for therapy of ocular sarcoidosis: report of a case

机译:小剂量糖皮质激素联合甲氨蝶呤治疗眼结节病:一例报告

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摘要

Sarcoidosis is a multisystem granulomatous disease of unknown etiology. Ocular involvement can be the initial manifestation, occurring by itself, or it can be associated with other systemic signs of sarcoidosis. A 31 years-old caucasian female presented a 10-day history of decreased vision and pain in OS. Biomicroscopy revealed fine keratic precipitates, a mild reaction in the anterior chamber and in the vitreous cavity in both eyes and a small posterior synechiae in OS. Intraocular pressure was 12 mmHg in the OD and 9 mmHg in OS. Fundoscopy disclosed mild swollen and hyperemic optic discs and some subretinal yellowish nodules of 1/3 to 1 disc diameter, partially delimited, located in the posterior pole and midperiphery in both eyes. The Chest X-ray disclosed the suspicion of hilar lymphadenopathy, especially on the left-side. The positron emission tomography (PET-scan) showed increased 18 F-fluorodeoxyglucose uptake in the paratracheal and bilateral hilar lymph nodes, indicating high local cellular metabolism. A mediastinal lymph node biopsy was performed afterwards, which depicted non-caseating granulomas with multinucleated giant cells and absence of acid-alcohol resistant bacilli. The patient was initially treated with oral prednisone 60 mg/day with slow tapering over the next months. A decreased papillitis and an increased size of the choroidal granulomas was observed after a 6-month therapy (Figs. 1B and 2B). Then, a combination of methotrexate 20 mg/week and prednisone 10 mg/day was given over the following months, which led to a gradual reduction in size and thickness of the choroidal granulomas. A weak response to steroid monotherapy was initially observed in this patient. The introduction of a non-steroid immunosuppressant drug (methotrexate) was associated with significant anatomic improvement in the following months. This report raises the suggestion that an early introduction of a nonsteroidal immunosuppressive drug to systemic steroids may be beneficial for a rapid remission of the uveitis.
机译:结节病是一种病因不明的多系统肉芽肿性疾病。眼部受累可以是其自身发生的最初表现,也可以与结节病的其他全身症状相关。一名31岁的白种女性出现了10天视力下降和OS疼痛的病史。生物显微镜检查显示,角膜上有良好的沉淀物,两只眼睛的前房和玻璃体腔内有轻度反应,OS中有小的后粘连。眼内压在OD中为12 mmHg,在OS中为9 mmHg。眼底镜检查发现轻度肿胀和充血性视盘,以及部分界定的位于双眼后极和中周的一些视网膜下浅黄色结节,其直径为盘状部分的1/3至1。胸部X光片显示怀疑肺门淋巴结肿大,尤其是在左侧。正电子发射断层显像(PET扫描)显示气管旁和双侧肺门淋巴结中18 F-氟脱氧葡萄糖摄取增加,表明局部细胞代谢较高。此后进行了纵隔淋巴结活检,该活检描绘了非干酪性肉芽肿,多核巨细胞,无酸-酒精抗性杆菌。该患者最初接受口服泼尼松60 mg /天的治疗,随后几个月逐渐减量。经过6个月的治疗,观察到乳头炎减少,脉络膜肉芽肿增大(图1B和2B)。然后,在接下来的几个月中联合使用甲氨蝶呤20 mg /周和泼尼松10 mg / day,这导致脉络膜肉芽肿的大小和厚度逐渐减小。最初在该患者中观察到对类固醇单一疗法的反应较弱。在接下来的几个月中,非甾体类免疫抑制剂药物(甲氨蝶呤)的引入与明显的解剖学改善相关。该报告提出了这样的建议,即将非甾体类免疫抑制药物尽早引入全身性类固醇可能有益于葡萄膜炎的快速缓解。

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