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Open AccessJournal ArticleDOI

Central Nervous System Manifestations of Cardiac Myxoma

Vivien H. Lee, +2 more
- 01 Aug 2007 - 
- Vol. 64, Iss: 8, pp 1115-1120
TLDR
In this paper, the authors retrospectively reviewed the medical records of 74 consecutive patients with pathologically confirmed cardiac myxoma at the Mayo Clinic from January 1, 1993, through December 31, 2004.
Abstract
Background Neurologic complications can be the initial manifestation of atrial myxoma. Prompt diagnosis is of paramount significance to prevent recurrent complications. Objective To identify patients with neurologic complications attributed to atrial myxoma. Design, Setting, and Patients With institutional review board approval, we retrospectively reviewed the medical records of 74 consecutive patients with pathologically confirmed cardiac myxoma at the Mayo Clinic from January 1, 1993, through December 31, 2004. Main Outcome Measures Discharge and follow-up modified Rankin score. Results Nine of the 74 patients with cardiac myxoma (12%) presented with neurologic manifestations in the setting of atrial myxoma. Mean age was 48.5 years (range, 17-70 years). There were 6 females and 3 males. Among patients with myxoma and neurologic symptoms, ischemic cerebral infarct was the most common neurologic manifestation (8 patients [89%]). No patients had concomitant cardiac symptoms. The size of the atrial myxoma was variable, with a mean diameter of 2.7 (range, 0.4-6.5) cm. Most of the atrial myxomas causing neurologic symptoms demonstrated a mobile component on transesophageal echocardiography (8 patients [89%]). Two patients (22%) had pathologic evidence of systemic myxomatous emboli. One patient with intracerebral hemorrhage had pathologically confirmed intracranial metastatic myxoma and myxoma-induced aneurysmal dilatation. Conclusions Neurologic complications are associated with cardiac myxoma in some patients with myxoma and, when they occur, frequently present with cerebral infarction. The mobility, not the size, of the myxoma appears to be related to embolic potential. Potential delayed neurologic complications relevant to patients with tumor embolization include myxoma-induced cerebral aneurysm and myxomatous metastasis, which can mimic the clinical picture of central nervous system vasculitis or infective endocarditis.

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References
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Journal ArticleDOI

The complex of myxomas, spotty pigmentation, and endocrine overactivity.

TL;DR: The overlap, in this sizeable number of patients, of various combinations of the same rare or very rare conditions unlikely to occur together by chance with any degree of frequency is striking evidence for a unique syndrome.
Journal ArticleDOI

Clinical presentation of left atrial cardiac myxoma. A series of 112 consecutive cases.

TL;DR: Myxomas in patients presenting with embolism have a friable surface; those in patients with cardiac symptoms, pseudo-mitral auscultation signs, tumor plop, and electrocardiogram or radiologic signs of left atrium hypertrophy and dilatation are significantly the larger tumors.
Journal ArticleDOI

Dominant Inheritance of the Complex of Myxomas, Spotty Pigmentation, and Endocrine Overactivity

TL;DR: At least one manifestation of the complex of myxomas, spotty pigmentation, and endocrine overactivity has occurred in three successive generations of this family.

Atrial myxomas: a review of clinical experience in 40 patients.

TL;DR: Echocardiography should be performed on all young patients with embolic disease and on those in whom the diagnosis of myxoma needs to be ruled out before exploratory or definitive surgery is undertaken so that unnecessary and potentially serious complications can be avoided.
Journal ArticleDOI

Cardiac myxoma. A clinicopathologic study.

TL;DR: The histology of myxomas varied by site, clinical presentation, patient age, and immunohistochemical findings, however, they were not likely to be histologically atypical, cellular, or incompletely excised.
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