Drixie D Vargas, Jenny M Garzón, María Cristina Martínez-Ávila, Juan D H Zuluaga, Carolina Sotelo
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Transthoracic echocardiography showed normal left ventricular function and a hypermobile interatrial septum. Transesophageal echocardiography confirmed the presence of a tunnel-shaped patent foramen ovale (PFO; 0.4 mm × 0.3 mm) without thrombus. No deep vein thrombosis or other embolic sources were found. A diagnosis of cardioembolic stroke due to paradoxical embolism through a PFO was established. The patient underwent successful percutaneous closure and started dual antiplatelet therapy. At follow-up, AHS symptoms improved significantly. This case highlights an atypical initial presentation of ischemic stroke in a young adult and emphasizes the need for early neuroimaging and comprehensive cardiac evaluation in cryptogenic strokes.</p>","PeriodicalId":10357,"journal":{"name":"Clinical Medicine Insights. 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We report the case of a 33-year-old male with no previous medical history who presented with involuntary movements of the left upper limb, describing it as \\\"moving on its own.\\\" Neurological examination was unremarkable, but MRI revealed multiple cortical infarcts in the right frontal and parietal lobes, with both acute and subacute features. Extensive workup ruled out vascular stenosis, dissection, and hypercoagulable states. Transthoracic echocardiography showed normal left ventricular function and a hypermobile interatrial septum. Transesophageal echocardiography confirmed the presence of a tunnel-shaped patent foramen ovale (PFO; 0.4 mm × 0.3 mm) without thrombus. No deep vein thrombosis or other embolic sources were found. A diagnosis of cardioembolic stroke due to paradoxical embolism through a PFO was established. The patient underwent successful percutaneous closure and started dual antiplatelet therapy. At follow-up, AHS symptoms improved significantly. 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引用次数: 0
摘要
异手综合征(AHS)是一种罕见的神经系统疾病,其特征是肢体在没有意识控制的情况下不自主地、有目标地运动。它通常与特定大脑区域的中风有关,包括内侧额叶和顶叶皮质。我们报告一例33岁男性,既往无病史,表现为左上肢不自主运动,描述为“自行移动”。神经学检查无明显异常,但MRI显示右侧额叶和顶叶多发皮质梗死,具有急性和亚急性特征。广泛的检查排除了血管狭窄、夹层和高凝状态。经胸超声心动图显示左心室功能正常,心房间隔过度活动。经食管超声心动图证实存在一隧道状卵圆孔未闭(PFO; 0.4 mm × 0.3 mm),无血栓。未发现深静脉血栓或其他栓塞源。诊断心脏栓塞性中风由于矛盾栓塞通过PFO被建立。患者成功经皮闭合并开始双重抗血小板治疗。随访时,AHS症状明显改善。本病例强调了年轻成人缺血性卒中的非典型初始表现,并强调了隐源性卒中早期神经影像学和全面心脏评估的必要性。
Alien Hand Syndrome as the Initial Presentation of Patent Foramen Ovale-Associated Stroke.
Alien Hand Syndrome (AHS) is a rare neurological condition characterized by involuntary, goal-directed movements of a limb without conscious control. It is most often associated with stroke in specific brain regions, including the medial frontal and parietal cortices. We report the case of a 33-year-old male with no previous medical history who presented with involuntary movements of the left upper limb, describing it as "moving on its own." Neurological examination was unremarkable, but MRI revealed multiple cortical infarcts in the right frontal and parietal lobes, with both acute and subacute features. Extensive workup ruled out vascular stenosis, dissection, and hypercoagulable states. Transthoracic echocardiography showed normal left ventricular function and a hypermobile interatrial septum. Transesophageal echocardiography confirmed the presence of a tunnel-shaped patent foramen ovale (PFO; 0.4 mm × 0.3 mm) without thrombus. No deep vein thrombosis or other embolic sources were found. A diagnosis of cardioembolic stroke due to paradoxical embolism through a PFO was established. The patient underwent successful percutaneous closure and started dual antiplatelet therapy. At follow-up, AHS symptoms improved significantly. This case highlights an atypical initial presentation of ischemic stroke in a young adult and emphasizes the need for early neuroimaging and comprehensive cardiac evaluation in cryptogenic strokes.