肌瘤导致多发性颅内动脉瘤和认知能力下降:病例报告

Sudipta Mondal, Prabhu Selvaraj, Asish Vijayaraghavan, Viswanadh S. V. G. Kalaparti, Deepti Narasimhaiah
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摘要

在心脏肌瘤病例中出现脑动脉瘤的情况非常罕见,全世界报告的病例不到 60 例。鉴于其罕见性,治疗方案仍有待商榷。我们介绍了一例年轻女性继发于心房肌瘤的多发性颅内动脉瘤病例,并简要回顾了相关文献。病例介绍 一位 30 多岁的年轻女性,8 年前曾有右侧大脑中动脉境界部中风的病史,在过去几年中逐渐出现全颅性头痛、注意力不集中和健忘等症状。在神经影像学检查中,她被发现患有多区域腔隙性脑梗塞和多发性颅内动脉瘤,数字减影血管造影证实了这一点。心脏检查发现了左心房肌瘤。皮层下认知功能衰退和颅内动脉瘤的病因是肌瘤和继发性肌瘤栓塞。其他继发性病因已被排除。肌瘤切除后,她一直接受药物随访。颅内动脉瘤是心脏肌瘤的罕见并发症,可能在肌瘤确诊前、同时或多年后出现。非特异性神经系统症状偶尔是颅内动脉瘤的不祥征兆,这就要求对心脏肌瘤病例进行神经影像学检查的门槛较低。由于缺乏明确的风险因素和不清楚的自然史,临床和放射学随访至关重要。学习要点
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myxomatous cause of multiple intracranial aneurysms and cognitive decline: a case report
The occurrence of cerebral aneurysm in a case of cardiac myxoma is rare with less than 60 cases reported worldwide. The course of management is still debatable given its rarity. We present a case of multiple intracranial aneurysms secondary to atrial myxoma in a young lady with a brief review of the literature. Case presentation A young lady in her late 30s with a history of right middle cerebral artery territory stroke eight years ago presented with gradually progressive symptoms in the form of holocranial headache, inattention and forgetfulness for the last few years. On neuroimaging, she was found to have multi-territorial lacunar infarcts and multiple intracranial artery aneurysms which was confirmed with a digital subtraction angiogram. A cardiac evaluation revealed a left atrial myxoma. The aetiology of subcortical cognitive decline and intracranial aneurysms was attributed to the myxoma with secondary myxomatous embolism. Other secondary causes were ruled out. She is being followed up medically after resection of the myxoma. Intracranial aneurysms are rare complications of cardiac myxoma which may present before, concurrent or many years after diagnosis of the myxoma. Nonspecific neurological complaints occasionally are the ominous signs of intracranial aneurysms which mandate a low threshold for neuroimaging in a case of cardiac myxoma. Given the absence of definitive risk factors and unclear natural history, clinical and radiological follow-ups are critical. Learning Points
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