Case Report
Cardiac Papillary Fibroelastoma: Source of Cerebral Embolism Treated With Intravenous Thrombolysis

https://doi.org/10.1016/j.jstrokecerebrovasdis.2010.02.013Get rights and content

We present the case of a 41-year-old man with sudden development of left hemiparesis due to infarction of the right middle cerebral artery that was successfully treated with intravenous (IV) thrombolysis with alteplase. Transthoracic echocardiography showed a small mass in the left ventricle. The patient underwent surgical resection, and histological examination of the mass confirmed the diagnosis of papillary fibroelastoma. It remains to be investigated whether heart ultrasound evaluation should be performed before IV thrombolysis in selected patients with stroke, given the apparently increased risk of bleeding. However, IV thrombolysis should not be postponed due to a lengthy investigation, because of its potential for reducing morbidity in patients with stroke.

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Case Report

A 41-year-old man with no history of serious illness and no known cerebrovascular risk factors was admitted after sudden development of left hemiparesis. Brain multislice computed tomography (MSCT) showed no early signs of stroke (Fig 1, A). On evaluation, the patient was assigned a National Institutes of Health Stroke Scale (NIHSS) score of 13. According to our institution's protocol, we started thrombolysis with IV tissue plasminogen activator (tPA) at 105 minutes after symptom onset.

Discussion

Cardiac PFE is a rare primary cardiac tumor. Unlike in myxoma, embolization is uncommon.2 It occurs mainly in persons over age 50 years, with no sex preference, and typically is asymptomatic or becomes evident during investigation after stroke.2, 3 Although rare, stroke is possible sequela of cardiac PFE. A fibrin thrombus attached to the edge of the PFE, as well as the PFE itself, can be sources of embolic material.2 Similarily, emboli from atrial myxomas may be composed of thrombus, tumor

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Cited by (8)

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    2016, Journal of Stroke and Cerebrovascular Diseases
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    Histologically confirmed tumor fragments have been isolated from the embolic material from coronary, pulmonary, and peripheral arteries, but not from cerebral embolism.2 Five cases are reported in literature in which PEF is supposed to be the stroke etiology treated with both IV3,4 and intra-arterial recombinant tissue plasminogen activator,5,6 and 2 of these cases are associated with mechanical disruption,6,7 but none of the 5 cases has the histological confirmation of the embolic material. In these cases, an indirect diagnosis of the embolic nature of the thombus was made by histological analysis after cardiac PEF removal.

  • Stroke and cardiac papillary fibroelastoma: Mechanical thrombectomy after thrombolytic therapy

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    Because of its rarity, there are few data regarding safety and efficacy of thrombolytic therapy in acute ischemic strokes caused by CPF. Only 3 previous reports presented patients with acute ischemic stroke and associated CPF treated with thrombolytic therapy—1 received alteplase intravenously3 and 2 intra-arterially4,5—in one of them intra-arterially thrombolysis was combined with mechanical clot disruption.5 When embolization is from the thrombotic material surrounding the neoplasm, it could be successfully treated with alteplase; if the embolizing material is a fragment from the tumor, fibrinolytic therapy is probably futile.

  • Neurologic complications of cardiac tumors

    2014, Handbook of Clinical Neurology
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    Results of thrombolytic therapy in embolic stroke from atrial myxoma have been mixed. A few case reports have described successful treatment of stroke from probable embolic disease using intravenous thrombolysis (Nagy et al., 2009; Abe et al., 2011; Malijevic et al., 2011; Ong and Chang, 2011) and intra-arterial thrombolysis (Gassanov et al., 2011). Other authors have described lack of success or intracranial hemorrhage from both intravenous and interarterial thrombolysis in similar patients (Bekavac et al., 1997; Chong et al., 2005; Acampa et al., 2011; Kohno et al., 2012).

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The authors have no conflicts of interest to disclose.

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