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尿毒症性脑干脑炎样表现酷似眼肌型重症肌无力:病例报告。

Uraemic brainstem encephalopathy mimicking ocular myasthenia: a case report.

机构信息

Professorial Unit in Medicine, National Hospital of Sri Lanka, Colombo, 01000, Sri Lanka.

Department of Clinical Medicine, University of Colombo, 25, Kynsey Road, Colombo, 00800, Sri Lanka.

出版信息

BMC Neurol. 2024 Apr 12;24(1):121. doi: 10.1186/s12883-024-03626-y.

Abstract

BACKGROUND

Uraemia causes a generalised encephalopathy as its most common neurological complication. Isolated brainstem uraemic encephalopathy is rare. We report a case of fatigable ptosis and complex ophthalmoplegia in brainstem uraemic encephalopathy.

CASE PRESENTATION

A 22-year-old Sri Lankan man with end stage renal failure presented with acute onset diplopia and drooping of eyelids progressively worsening over one week. The patient had not complied with the prescribed renal replacement therapy which was planned to be initiated 5 months previously. On examination, his Glasgow coma scale score was 15/15, He had a fatigable asymmetrical bilateral ptosis. The ice-pack test was negative. There was a complex ophthalmoplegia with bilateral abduction failure and elevation failure of the right eye. The diplopia did not worsen with prolonged stare. The rest of the neurological examination was normal. Serum creatinine on admission was 21.81 mg/dl. The repetitive nerve stimulation did not show a decremental pattern. Magnetic resonance imaging (MRI) of the brain demonstrated diffuse midbrain and pontine oedema with T2 weighted/FLAIR hyperintensities. The patient was haemodialyzed on alternate days and his neurological deficits completely resolved by the end of the second week of dialysis. The follow up brain MRI done two weeks later demonstrated marked improvement of the brainstem oedema with residual T2 weighted/FLAIR hyperintensities in the midbrain.

CONCLUSIONS

Uraemia may rarely cause an isolated brainstem encephalopathy mimicking ocular myasthenia, which resolves with correction of the uraemia.

摘要

背景

尿毒症是最常见的神经系统并发症之一,可引起全身性脑病。孤立性脑干尿毒症脑病较为罕见。我们报告一例脑干尿毒症脑病导致的易疲劳性眼睑下垂和复杂眼球运动障碍。

病例介绍

一名 22 岁的斯里兰卡男性患有终末期肾衰竭,急性发作复视和眼睑下垂,症状逐渐加重,持续了一周。患者未遵守规定的肾脏替代治疗方案,该方案原计划在 5 个月前开始。检查时,格拉斯哥昏迷量表评分为 15/15,患者有易疲劳性双侧不对称性眼睑下垂。冰袋试验为阴性。存在复杂的眼球运动障碍,表现为双侧外展无力和右眼上抬无力。长时间凝视并不会使复视加重。其余神经系统检查正常。入院时血清肌酐为 21.81mg/dl。重复神经刺激未显示递减模式。脑部磁共振成像(MRI)显示弥漫性中脑和桥脑水肿,T2 加权/FLAIR 呈高信号。患者隔天接受血液透析,透析第二周结束时,其神经功能缺损完全缓解。两周后进行的随访脑部 MRI 显示脑干水肿明显改善,中脑仍残留 T2 加权/FLAIR 高信号。

结论

尿毒症罕见情况下可引起孤立性脑干脑病,表现类似于眼肌型重症肌无力,纠正尿毒症后可缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c243/11010437/94806b0f1031/12883_2024_3626_Fig1_HTML.jpg

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