一名患有慢性后葡萄膜炎的年轻人因霉酚酸酯诱发淋巴组织增生性疾病。

IF 0.5 Q4 OPHTHALMOLOGY Journal of VitreoRetinal Diseases Pub Date : 2024-10-30 DOI:10.1177/24741264241294165
Nabiha B Habib, Joseph Boss
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引用次数: 0

摘要

目的:介绍一例因 Vogt-Koyanagi-Harada(VKH)病引起的双侧慢性后葡萄膜炎患者,患者曾接受霉酚酸酯治疗,但随后右眼发生玻璃体视网膜淋巴瘤。方法:对一个病例及其结果进行分析。结果:一名 34 岁的西班牙裔女性因继发于 VKH 病,双眼慢性复发性后葡萄膜炎病史长达 8 年。右眼出现玻璃体浸润,且对治疗耐药。随后,医生对其进行了诊断性玻璃体切除术,确定患者患上了单侧玻璃体视网膜淋巴瘤。结论:对于接受免疫调节治疗的已确诊葡萄膜炎患者,假性综合征仍应在鉴别诊断之列。当治疗反应不典型时,应考虑进行诊断性玻璃体切除术。此外,目前还缺乏针对青壮年孤立性单侧眼内淋巴瘤的中枢神经系统预防指南。
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Mycophenolate Mofetil-Induced Lymphoproliferative Disorder in a Young Adult With Chronic Posterior Uveitis.

Purpose: To present a case of a young adult with bilateral chronic posterior uveitis resulting from Vogt-Koyanagi-Harada (VKH) disease treated with mycophenolate mofetil who subsequently developed vitreoretinal lymphoma in the right eye. Methods: A case and its findings were analyzed. Results: A 34-year-old Hispanic woman presented with an 8-year history of chronic recurrent posterior uveitis in both eyes secondary to VKH disease. A vitreous infiltrate that was treatment resistant occurred in the right eye. Subsequently, a diagnostic vitrectomy was performed, and it was determined that the patient had developed unilateral vitreoretinal lymphoma. Conclusions: Masquerade syndromes should remain in the differential in patients with well-established uveitis who are on immunomodulatory treatment. A diagnostic vitrectomy should be considered when the treatment response is uncharacteristic. Furthermore, guidelines are lacking for central nervous system prophylaxis for isolated unilateral ocular intraocular lymphoma in young adults.

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