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伴有双侧中心静脉闭塞的短暂性偏侧神经痛性麻木发作

HaNDL with bilateral central venous occlusions.

作者信息

Wang Wendy, Mack Heather G, Stawell Richard, White Owen, Waterston John

机构信息

Neurology, Alfred Hospital, Melbourne, Victoria, Australia.

Department of Surgery (Ophthalmology), The University of Melbourne, Melbourne, Victoria, Australia.

出版信息

BMJ Neurol Open. 2020 Jun 2;2(1):e000043. doi: 10.1136/bmjno-2020-000043. eCollection 2020.

Abstract

BACKGROUND

The syndrome of Headache and focal Neurological Deficits with cerebrospinal fluid Lymphocytosis (HaNDL) is considered a rare, idiopathic and self-limited condition.

METHODS

We present a patient with HaNDL who had unique findings of florid optic disc haemorrhages from bilateral central retinal vein occlusions.

RESULTS

Our patient made a full recovery with conservative management.

CONCLUSION

It is important for medical attendants to recognise that HaNDL syndrome can be associated with neuro-ophthalmic complications.

摘要

背景

伴有脑脊液淋巴细胞增多的头痛和局灶性神经功能缺损综合征(HaNDL)被认为是一种罕见的、特发性的自限性疾病。

方法

我们报告了一名患有HaNDL的患者,其具有双侧视网膜中央静脉阻塞导致的明显视盘出血这一独特表现。

结果

我们的患者通过保守治疗完全康复。

结论

医护人员认识到HaNDL综合征可能与神经眼科并发症相关很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6414/7871729/c93dd425d71c/bmjno-2020-000043f01.jpg

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