PRIMARY RIGHT ATRIAL CARDIAC ANGIOSARCOMA INITIALLY PRESENTING AS SYNCOPE
نویسندگان
چکیده
منابع مشابه
Primary Cardiac Angiosarcoma Presenting With Cardiac Tamponade
Primary cardiac angiosarcoma is a very rare disease with a poor prognosis. We report a case of a patient with a primary cardiac angiosarcoma who presented with cardiac tamponade; the angiosarcoma was successfully resected surgically.
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Primary cardiac angiosarcoma is a rare tumor associated with a poor prognosis. We report a case of a 59-year-old woman with right atrial angiosarcoma presenting with cardiac tamponade due to right atrial perforation. She underwent urgent surgical resection of the tumor. However, the patient died 68 days after surgery due to local recurrence. An effective treatment for cardiac angiosarcoma has n...
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Angiosarcoma of the heart is a rare malignancy that can present in many ways. It is an important diagnosis to consider in patients presenting with otherwise unexplained tamponade-type symptoms. Here we present a case of a young male who presented with hemorrhagic tamponade and underwent resection of a large angiosarcoma of the right atrium. In this case, we describe the rare presentation of ang...
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We describe a case of right atrial myxoma in a 62-year-old woman presenting with syncope. The patient had a 4-month history of syncope and felt faint on lying flat in bed before the admission. Transthoracic and transesophageal echocardiography showed a large right atrial mass that was prolapsing through the tricuspid valve into the right ventricle during diastole. Coronary angiography revealed ...
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primary cardiac sarcomas are very rare and there is no consensus on management. clinical presentation is usually late. despite newer diagnostic technology, prognosis remains dismal. we report a case of right atrial sarcoma in a 28-year-old man who presented with acute cardiac tamponade. emergency subxiphoid pericardial drainage stabilized the patient's critical condition. the lesion was advance...
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ژورنال
عنوان ژورنال: Chest
سال: 2019
ISSN: 0012-3692
DOI: 10.1016/j.chest.2019.08.1086