Cardiac lymphangioma: case report and review of the literature |
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Authors: | Kaji Tatsuru Takamatsu Hideo Noguchi Hiroyuki Tahara Hiroyuki Matsuda Hiromitsu Nomura Yuichi Machigashira Shouko Watanabe Shunichi Yoshioka Takako |
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Affiliation: | From the Department of Pediatric Surgery, Pediatrics, the Second Surgery, the first Pathology, Faculty of Medicine, Kagoshima University, Kagoshima City, Japan. |
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Abstract: | Cardiac lymphangioma is uncommon and constitutes one of the rare forms of cardiac diseases. A 6-year-old girl had an abnormal electrocardiogram in a screening test on admission to an elementary school. Echocardiogram, computed tomogram, and magnetic resonance imaging showed a mediastinal multicystic mass that was adjacent to the left ventricle of the heart. The tumor was found to be originated in myocardium by left thoracotomy and pericadiotomy. A partial resection of tumor and a pericardial window were done. This case, to the authors' knowledge, represents the sixth reported case of cardiac lymphangioma. J Pediatr Surg 37:E32. |
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