| Literature DB >> 12378478 |
Tatsuru Kaji1, Hideo Takamatsu, Hiroyuki Noguchi, Hiroyuki Tahara, Hiromitsu Matsuda, Yuichi Nomura, Shouko Machigashira, Shunichi Watanabe, Takako Yoshioka.
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. Copyright 2002, Elsevier Science (USA). All rights reserved.Entities:
Mesh:
Year: 2002 PMID: 12378478 DOI: 10.1053/jpsu.2002.35445
Source DB: PubMed Journal: J Pediatr Surg ISSN: 0022-3468 Impact factor: 2.545