Key result
Surgical resection successfully treats left atrial myxoma presenting as ischemic stroke.
Why the study?
Cardiac myxoma is a rare source of cerebral stroke in young subjects.
Case Report (n=1)
No
Left atrial myxoma is a rare but important cause of ischemic stroke in young patients, highlighting the critical role of transthoracic echocardiography in the etiological work-up.
Supports echocardiography in young stroke work-up; leaves open prospective validation of screening protocols.
Introduction: Cardiac myxoma is a primary benign tumor most often located in the left atrium and it is a rare source of cerebral stroke of young subjects. Case Presentation: We report the case of a young women with cardiac myxoma revelated by hemiplegia. The patient suddenly presented vertigo followed by a fall, a heaviness of her left body, and dysarthria. The brain CT scan and magnetic resonance imaging have revealed cerebral ischemia located in the right Sylvian territory. Transthoracic echocardiography highlighted a round cardiac mass, mobile, heterogeneous, multilobed, appended to the interatrial septum and the atrial side of the large mitral valve by wide implantation and measuring 38x25mm in the parasternal short axis (PSAX) and apical 4 chamber views evocative of left atrium myxoma. After the surgical resection, which was postponed for a month, the removed tumor was sent for histopathological examination. The morphological examination revealed a myxoid tumor proliferation compatible with cardiac myxoma expressing calretinin by these tumor cells in the immunohistochemical study. Conclusions: Left atrium myxoma is a benign cardiac tumor and a rare cause of ischemic stroke. Transthoracic echocardiography facilitates the diagnosis of this tumor which will then be confirmed by histological analysis.
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Charfo et al. (2022) conducted a case report in Left atrial myxoma and ischemic stroke (n=1). Surgical resection was evaluated. A 46-year-old woman presenting with an ischemic stroke was diagnosed with a left atrial myxoma, which was successfully treated with surgical resection.
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