When a Hypersomnolent Hemodialyzed Patient Actually Has a Rare Stroke: A Case of Artery of Percheron Infarction With Paradoxical Embolism.

IF 1.1 4区 医学 Q4 CLINICAL NEUROLOGY
Filipe Oliveira Pinheiro, Ruben Reis Maia, Delfim Duarte, Ana Monteiro, Jorge Almeida
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引用次数: 0

Abstract

Introduction: Artery of Percheron (AOP) is an uncommon anatomic variant of the arterial supply of the medial thalami. Owing to variable clinical presentation, challenging imaging diagnosis, and its rarity, it is difficult to diagnose AOP infarctions. We present a clinical case of a unique presentation of AOP infarction associated with paradoxical embolism and highlight the atypical clinical manifestations and challenging diagnosis of this stroke syndrome.

Case report: A 58-year-old White female with chronic renal insufficiency on hemodialysis was admitted to our center with a 10-hour course of hypersomnolence and right-sided ataxia. She had normal body temperature, blood pressure, peripheral oxygen saturation, and heart rate and scored 11 points in the Glasgow Coma Scale and 12 points in National Institutes of Health Stroke Scale. Initial brain computerized tomography scan, electrocardiogram, and thoracic radiography were normal; transcranial Doppler ultrasound showed >50% stenosis at the P2 segment of the right posterior cerebral artery, and transthoracic echocardiogram, a patent foramen ovale and thrombus adherent to the hemodialysis catheter. On day 3, she underwent brain magnetic resonance that showed acute ischemic lesions at the paramedian thalami and the superior cerebral peduncles. AOP infarction due to a paradoxical embolism from a patent foramen ovale with a right atrial thrombus was the final diagnosis.

Conclusions: AOP infarctions are a rare type of stroke with elusive clinical presentations and frequently, initial imaging assessment is normal. Early recognition is crucial, and a high index of suspicion is needed to suspect this diagnosis.

当一名高嗜睡血液透析患者实际上患有罕见的中风时:一例并发悖论性栓塞的Percheron梗死动脉。
引言:Percheron动脉(AOP)是丘脑内侧动脉供应的一种不常见的解剖学变体。由于临床表现多变,影像学诊断具有挑战性,且其罕见性,诊断AOP梗死很困难。我们提出了一个临床病例,其独特的AOP梗死表现与反常栓塞相关,并强调了这种中风综合征的非典型临床表现和具有挑战性的诊断。病例报告:一名58岁的白人女性,患有血液透析中的慢性肾功能不全,因嗜睡和右侧共济失调入院10小时。她的体温、血压、外周血氧饱和度和心率正常,在格拉斯哥昏迷量表中得了11分,在美国国立卫生研究院中风量表中得12分。最初的脑部计算机断层扫描、心电图和胸部放射线检查均正常;经颅多普勒超声显示右侧大脑后动脉P2段狭窄>50%,经胸超声心动图显示卵圆孔未闭,血栓粘附在血液透析导管上。第3天,她接受了脑部磁共振检查,结果显示丘脑旁正中和大脑上脚有急性缺血性病变。由卵圆孔未闭伴右心房血栓的反常栓塞引起的AOP梗死是最终诊断。结论:AOP梗死是一种罕见的中风类型,其临床表现难以捉摸,通常情况下,初步影像学评估正常。早期识别至关重要,需要高怀疑指数来怀疑这种诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurologist
Neurologist 医学-临床神经学
CiteScore
1.90
自引率
0.00%
发文量
151
审稿时长
2 months
期刊介绍: The Neurologist publishes articles on topics of current interest to physicians treating patients with neurological diseases. The core of the journal is review articles focusing on clinically relevant issues. The journal also publishes case reports or case series which review the literature and put observations in perspective, as well as letters to the editor. Special features include the popular "10 Most Commonly Asked Questions" and the "Patient and Family Fact Sheet," a handy tear-out page that can be copied to hand out to patients and their caregivers.
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