Wang Aihua, Wang Zhaoxia, Hu Ke, Liu Jinzhi, Cao Qiwei, Zhang Zixian, Si Zhihua
Department of Neurology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Neuroimmunology, Shandong Key Laboratory of Rheumatic Disease and Translational Medicine, Jinan, China.
Department of Neurology, Juxian People's Hospital, Rizhao, China.
Transl Pediatr. 2022 Jan;11(1):149-156. doi: 10.21037/tp-21-11.
Intracranial aneurysm may appear even after the removal of the cardiac myxoma. However, the pathogenesis and treatment of such aneurysm lesions are not clear. The study aimed to explore the clinical and imaging manifestation, hypothetical pathogenesis, and therapy in one case of left atrial myxoma causing multiple intracranial aneurysms. A 14-year-old male displayed a 3-hour history of episodic loss of consciousness and right hemiplegia after a leapfrog-like movement. The myxoma was diagnosed by a combination of clinical examination, leading to the diagnosis of mitral dynamic obstruction with a Grade III mitral diastolic murmur and tumor plop; magnetic resonance imaging, revealing multiple ischemic sites in both semi-oval centers; and transthoracic echocardiography, demonstrating a mitral valve obstruction. The myxoma was removed surgically; however, computed tomography angiography showed multiple intracranial aneurysms in both middle cerebral arteries 18 months after resection of the atrial myxoma. After conservative treatment, the patient had no neurological dysfunction symptoms for 5 years after myxoma resection. His condition is relatively stable. In conclusion, resection of the atrial myxoma may eliminate the early neurological symptoms, but it cannot ensure the nonoccurrence of delayed intracranial aneurysms. The neoplastic process theory was favored for explaining the aneurysm development in this case. According to the specific conditions of the patient, a combination of open surgery, chemotherapy, radiotherapy, and coil embolization is recommended.
即使切除心脏黏液瘤后仍可能出现颅内动脉瘤。然而,此类动脉瘤病变的发病机制和治疗方法尚不清楚。本研究旨在探讨1例左心房黏液瘤导致多发颅内动脉瘤患者的临床及影像学表现、可能的发病机制和治疗方法。一名14岁男性在进行蛙跳样运动后出现3小时的发作性意识丧失和右侧偏瘫病史。通过临床检查、伴有III级二尖瓣舒张期杂音和肿瘤扑落音的二尖瓣动态梗阻诊断、磁共振成像显示双侧半卵圆中心多个缺血部位以及经胸超声心动图显示二尖瓣梗阻等综合手段确诊为黏液瘤。手术切除了黏液瘤;然而,心脏黏液瘤切除术后18个月的计算机断层扫描血管造影显示双侧大脑中动脉多发颅内动脉瘤。保守治疗后,患者在黏液瘤切除术后5年无神经功能障碍症状。其病情相对稳定。总之,切除心房黏液瘤可能消除早期神经症状,但不能确保不发生延迟性颅内动脉瘤。肿瘤形成过程理论更有利于解释该病例中动脉瘤的发生发展。根据患者的具体情况,建议采用开放手术、化疗、放疗和弹簧圈栓塞相结合的治疗方法。