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Primary cardiac tumors associated with genetic syndromes: a comprehensive review |
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| Authors: | Elizabeth?Lee mailto:echaripa@med.umich.edu" title=" echaripa@med.umich.edu" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author http://orcid.org/---" itemprop=" url" title=" View OrcID profile" target=" _blank" rel=" noopener" data-track=" click" data-track-action=" OrcID" data-track-label=" " >View author&# s OrcID profile,Maryam?Ghadimi?Mahani,Jimmy?C.?Lu,Adam?L.?Dorfman,Ashok?Srinivasan,Prachi?P.?Agarwal |
| Affiliation: | 1.Division of Cardiothoracic Radiology, Department of Radiology,University of Michigan Health System, University Hospital Floor B1 Reception C,Ann Arbor,USA;2.Section of Pediatric Radiology, C. S. Mott Children’s Hospital, Department of Radiology,University of Michigan Health System,Ann Arbor,USA;3.Section of Pediatric Cardiology, Department of Pediatrics,C. S. Mott Children’s Hospital, University of Michigan Health System,Ann Arbor,USA;4.Division of Neuroradiology, Department of Radiology,University of Michigan Health System,Ann Arbor,USA |
| Abstract: | Various cardiac tumors occur in the setting of a genetic syndrome such as myxomas in Carney complex and rhabdomyomas in tuberous sclerosis. Tumor biology can be different in syndromic forms, and on imaging children sometimes demonstrate additional manifestations of the underlying syndrome. We discuss the imaging appearance of cardiac tumors occurring in the framework of a genetic syndrome, the findings that suggest an underlying syndrome, and the impact on management. |
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