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帕克斯·韦伯综合征:足下垂的罕见病因。

Parkes Weber syndrome: a rare cause of foot drop.

作者信息

Kyriakides Demetra Elena, Michaelides Demos, Lambrianides Sakis

机构信息

Department of Medicine, James Cook University Hospital, Middlesbrough, UK

Radiology, Evresis Diagnostic Center, Nicosia, Cyprus.

出版信息

BMJ Case Rep. 2023 Oct 4;16(10):e254455. doi: 10.1136/bcr-2022-254455.

Abstract

This case report describes a patient in her late 60s, previously diagnosed with Klippel-Trenaunay syndrome who presented with difficulty walking. A year prior to her presentation she had a fall which made her notice a painless foot drop on the right. Her right leg was profoundly hypertrophied compared with the left, and a port-wine stain was present on the lateral side, extending from the hip to the mid-shin. The patient's differential diagnosis based on clinical examination and investigations is discussed leading to a final diagnosis of sciatic neuropathy secondary to an arteriovenous malformation due to Parkes Weber syndrome.

摘要

本病例报告描述了一位60多岁的女性患者,此前被诊断为克-特综合征,现出现行走困难。在就诊前一年,她发生了一次跌倒,之后注意到右侧出现无痛性足下垂。与左侧相比,她的右腿明显肥大,外侧有葡萄酒色斑,从臀部延伸至小腿中部。本文讨论了基于临床检查和检查结果对该患者的鉴别诊断,最终诊断为帕克斯·韦伯综合征所致动静脉畸形继发坐骨神经病变。

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Parkes Weber syndrome: a rare cause of foot drop.帕克斯·韦伯综合征:足下垂的罕见病因。
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