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强直性瞳孔:慢性炎症性脱髓鞘性多发性神经病(CIDP)中的一种不常见自主神经受累。

Tonic pupils: an unusual autonomic involvement in chronic inflammatory demyelinating polyneuropathy (CIDP).

机构信息

Department of Neurology, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Pedro de Toledo, 650, São Paulo, SP, 04039-002, Brazil.

出版信息

Neurol Sci. 2019 Aug;40(8):1725-1727. doi: 10.1007/s10072-019-03890-8. Epub 2019 Apr 17.

Abstract

BACKGROUND

Chronic inflammatory demyelinating polyneuropathy (CIDP) is a neuropathy which affects mainly large myelinated axons and has a typically mild autonomic dysfunction mainly from postganglionic nerve fiber involvement.

CASE REPORT

We report here an acute onset CIDP initially diagnosed as Guillain-Barré syndrome (GBS), unresponsive to treatment with intravenous immunoglobulin (IVIg), which later responded to plasmapheresis and corticoids. The patient had a markedly distal demyelination, prominent cranial nerve involvement and, interestingly, bilateral fixed dilated pupils. Despite complete clinical recovery, this neurological sign remained.

CONCLUSIONS

Tonic pupils have previously been described in different neurologic conditions, including GBS, but not yet in acute onset CIDP or in variants with predominantly distal demyelination. It differs from the classical Adie's pupil because it lacks the light-near dissociation. This case report expands the range of possible autonomic signs in acute onset CIDP, which could help physicians establish optimal treatment strategies earlier on.

摘要

背景

慢性炎症性脱髓鞘性多发性神经病(CIDP)是一种主要影响大髓鞘轴突的神经病,通常伴有轻度自主神经功能障碍,主要是节后神经纤维受累。

病例报告

我们在此报告一例最初诊断为吉兰-巴雷综合征(GBS)的急性 CIDP 病例,对静脉注射免疫球蛋白(IVIg)治疗无反应,后对血浆置换和皮质类固醇治疗有反应。该患者有明显的远端脱髓鞘、明显的颅神经受累,有趣的是,双侧固定性扩大瞳孔。尽管临床完全恢复,但该神经体征仍然存在。

结论

以往曾在包括 GBS 在内的不同神经疾病中描述过强直性瞳孔,但尚未在急性发作 CIDP 或主要表现为远端脱髓鞘的变异型中描述过。它与经典的阿狄森瞳孔不同,因为它缺乏光近分离。本病例报告扩展了急性发作 CIDP 中可能出现的自主神经体征范围,这可能有助于医生更早地制定最佳治疗策略。

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