Mondal Sudipta, Selvaraj Prabhu, Vijayaraghavan Asish, Kalaparti Viswanadh S V G, Narasimhaiah Deepti
Department of Cardiology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, India.
Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, India.
Egypt Heart J. 2024 Sep 16;76(1):130. doi: 10.1186/s43044-024-00559-2.
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 Intracranial aneurysms are rare complications of cardiac myxoma that may present before, concurrent or many years after diagnosis of the myxoma. Special attention must be given to nonspecific neurological complaints with a low threshold for neuroimaging in those with a prior history of cardiac myxoma. Given the absence of definitive risk factors and unclear natural history, clinical and radiological follow-up including conventional angiography and/or magnetic resonance imaging is critical.
心脏黏液瘤患者发生脑动脉瘤的情况罕见,全球报道不足60例。鉴于其罕见性,治疗方案仍存在争议。我们报告一例年轻女性因心房黏液瘤继发多发颅内动脉瘤的病例,并对相关文献进行简要回顾。病例介绍 一名30多岁的年轻女性,8年前有右侧大脑中动脉供血区卒中病史,在过去几年中出现逐渐加重的全颅头痛、注意力不集中和健忘等症状。神经影像学检查发现她有多区域腔隙性梗死和多发颅内动脉动脉瘤,数字减影血管造影证实了这一情况。心脏评估显示左心房黏液瘤。皮质下认知功能减退和颅内动脉瘤的病因归因于黏液瘤继发黏液瘤性栓塞。排除了其他继发原因。黏液瘤切除术后她正在接受医学随访。
颅内动脉瘤是心脏黏液瘤罕见的并发症,可在黏液瘤诊断之前、同时或多年后出现。非特异性神经症状偶尔是颅内动脉瘤的不祥征兆,对于心脏黏液瘤患者,应降低神经影像学检查的阈值。由于缺乏明确的危险因素且自然病史不明,临床和影像学随访至关重要。学习要点 颅内动脉瘤是心脏黏液瘤罕见的并发症,可在黏液瘤诊断之前、同时或多年后出现。对于有心脏黏液瘤病史的患者,必须特别关注非特异性神经症状,降低神经影像学检查的阈值。由于缺乏明确的危险因素且自然病史不明,包括传统血管造影和/或磁共振成像在内的临床和影像学随访至关重要。