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pubmed-article:1984944pubmed:abstractTextTwo cases of nonimmune hydrops fetalis and fetal death associated with cardiac rhabdomyoma are reported. Case 1 presented with fetal supraventricular tachycardia, and cardiac rhabdomyoma was accurately diagnosed by fetal echocardiography. Autopsy revealed multiple rhabdomyomata involving the right atrial free wall, the sinoatrial node, and the left ventricle. The left circumflex coronary artery was extrinsically compressed by adjacent tumor tissue, causing left ventricular myocardial infarction. Case 2 had a unique, pedunculated, ball-like rhabdomyoma that almost totally occluded the mitral orifice. The causes of fetal death in patients with cardiac rhabdomyoma are analyzed and the possibility of fetal surgical management is proposed.lld:pubmed
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pubmed-article:1984944pubmed:authorpubmed-author:Van PraaghRRlld:pubmed
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pubmed-article:1984944pubmed:pagination139-42lld:pubmed
pubmed-article:1984944pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:1984944pubmed:year1991lld:pubmed
pubmed-article:1984944pubmed:articleTitleCardiac rhabdomyoma. Rare cause of fetal death.lld:pubmed
pubmed-article:1984944pubmed:affiliationDepartment of Pathology, Children's Hospital, Boston.lld:pubmed
pubmed-article:1984944pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1984944pubmed:publicationTypeCase Reportslld:pubmed
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