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西罗莫司诱发的中毒性视神经病变。

Sirolimus Induced Toxic Optic Neuropathy.

作者信息

Pakravan Parastou, Miri Shahnaz, Lam Byron L

机构信息

Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, USA.

出版信息

Int Med Case Rep J. 2023 May 31;16:329-332. doi: 10.2147/IMCRJ.S388481. eCollection 2023.

Abstract

OBJECTIVE

To describe a case of optic neuropathy after prolonged sirolimus therapy in the setting of cardiac transplant.

BACKGROUND

Sirolimus is an immunosuppressant that inhibits Mechanistic Target of Rapamycin (mTOR) and blocks T-cell activation and B-cell differentiation by preventing response to Interleukin-2 (IL-2). Tacrolimus is another immunosuppressive agent, one of the known but uncommon side effects of which is bilateral optic neuropathy years after taking the medication. To the best of our knowledge, this is the first report of sequential optic neuropathy after years of treatment with sirolimus.

CASE PRESENTATION

A 69-year-old male with a history of cardiac transplantation presented with progressive, sequential, and painless vision loss. Visual acuity was 20/150 OD and 20/80 OS, with impaired color vision in both eyes (Ishihara 0/10) and bilateral disc pallor and mild optic disc edema in the left eye. Visual field was constricted in both eyes. The patient was on prolonged sirolimus therapy for over 7 years. Orbital MRI revealed bilateral chiasmatic thickness and FLAIR hyperintensity, without optic nerve enhancement post gadolinium. After extensive work up, other etiologies such as infectious, inflammatory, and neoplastic lesions were ruled out. Subsequently, sirolimus was substituted with cyclosporin that led to gradual improvement of vision and visual fields bilaterally.

CONCLUSION

Optic neuropathy is a rare side effect of tacrolimus, which has been seen as sudden, painless, and bilateral vision loss in post-transplant patients. Other concurrent medications influencing the cytochrome P4503A enzyme complexes may alter the pharmacokinetics of tacrolimus and increase the likelihood of toxicity. Discontinuation of offending agent has been shown to improve visual defects. We presented a rare case of optic neuropathy in a patient on sirolimus, whose visual defects improved upon discontinuation of sirolimus and switching to cyclosporin.

摘要

目的

描述一例心脏移植患者长期使用西罗莫司治疗后出现视神经病变的病例。

背景

西罗莫司是一种免疫抑制剂,可抑制雷帕霉素作用靶点(mTOR),并通过阻止对白细胞介素-2(IL-2)的反应来阻断T细胞活化和B细胞分化。他克莫司是另一种免疫抑制剂,其已知但不常见的副作用之一是用药数年之后出现双侧视神经病变。据我们所知,这是首例关于长期使用西罗莫司治疗后出现相继性视神经病变的报告。

病例介绍

一名有心脏移植病史的69岁男性患者,出现进行性、相继性且无痛性视力丧失。右眼视力为20/150,左眼视力为20/80,双眼色觉受损(石原氏色盲测试0/10)以及双侧视盘苍白,左眼有轻度视盘水肿。双眼视野均变窄。该患者长期使用西罗莫司治疗超过7年。眼眶磁共振成像显示双侧视交叉增厚以及液体衰减反转恢复序列(FLAIR)高信号,钆增强后视神经无强化。经过全面检查,排除了感染、炎症和肿瘤性病变等其他病因。随后,将西罗莫司换成环孢素,这使得双眼视力和视野逐渐改善。

结论

视神经病变是他克莫司的一种罕见副作用,在移植后患者中表现为突发、无痛性双侧视力丧失。其他影响细胞色素P4503A酶复合物的同时服用药物可能会改变他克莫司的药代动力学并增加毒性发生的可能性。停用致病药物已被证明可改善视觉缺陷。我们报告了一例使用西罗莫司的患者发生视神经病变的罕见病例,该患者停用西罗莫司并换用环孢素后视觉缺陷得到改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22e9/10239645/d5abc64823ea/IMCRJ-16-329-g0001.jpg

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