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枕叶出血后偏盲及巴林特综合征的特征:发病数年之后的识别及患者理解有助于功能改善

Hemianopia and Features of Bálint Syndrome following Occipital Lobe Hemorrhage: Identification and Patient Understanding Have Aided Functional Improvement Years after Onset.

作者信息

McDowell Nicola, Dutton Gordon N

机构信息

Institute of Education, Massey University, Albany Drive, Palmerston North 4474, New Zealand.

Department of Vision Sciences, Glasgow Caledonian University, Cowcaddens Road, Glasgow G4 0BA, UK.

出版信息

Case Rep Ophthalmol Med. 2019 Mar 25;2019:3864572. doi: 10.1155/2019/3864572. eCollection 2019.

Abstract

Cerebral visual impairment (CVI) can present around birth or any time thereafter. Homonymous hemianopia is a common feature. The concept that functional improvement is unattainable augurs against active management. Dorsal stream dysfunction (or Bálint syndrome when severe) results from bilateral posterior parietal dysfunction but may go undetected, especially in children. At 16 the patient suffered spontaneous left occipital lobe brain hemorrhage from a ruptured arteriovenous malformation. This was surgically excised. Short lived right upper limb intermittent jerking, with additional left sided weakness, ensued. Anomalous EEG recordings, with right-sided bias, arose from the posterior temporoparietal area. A right homonymous hemianopia was evident. During the ensuing 17 years she experienced multiple complex difficulties, until, at a lecture describing how to identify and support children with CVI, she realized she herself had many of the difficulties described. Visual assessment identified hemianopia and dorsal stream dysfunction. Following identification, characterization, and explanation of the impact of her visual difficulties, she both gained greater awareness of her visual difficulties and their impact and developed a range of strategies leading to functional improvement of her visual field loss and amelioration of her dorsal stream dysfunction, with great improvement in quality of life.

摘要

脑性视觉障碍(CVI)可在出生时或之后的任何时间出现。同向性偏盲是其常见特征。认为功能无法改善的观念不利于积极治疗。背侧流功能障碍(严重时为巴林特综合征)由双侧顶叶后部功能障碍引起,但可能未被发现,尤其是在儿童中。患者16岁时因动静脉畸形破裂发生自发性左枕叶脑出血,接受了手术切除。随后出现短暂的右上肢间歇性抽搐,并伴有左侧肢体无力。颞顶叶后部区域出现异常脑电图记录,右侧偏向。明显存在右同向性偏盲。在随后的17年里,她经历了多重复杂困难,直到在一次关于如何识别和支持患有CVI的儿童的讲座上,她意识到自己也有许多讲座中描述的困难。视力评估发现了偏盲和背侧流功能障碍。在对她的视力困难的影响进行识别、描述和解释后,她不仅对自己的视力困难及其影响有了更深刻的认识,还制定了一系列策略,使她的视野缺损功能得到改善,背侧流功能障碍得到缓解,生活质量有了很大提高。

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