Institutional members access full text with Ovid®

Share this article on:

Large Multifocal Cardiac Myxoma Causing the Sudden Unexpected Death of a 2-Month-Old Infant-A Rapidly Growing, Acquired Lesion Versus a Congenital Process?: A Case Report

Kure, Kiyoe MD, PhD*; Lingamfelter, Daniel DO*; Taboada, Eugenio MD

The American Journal of Forensic Medicine and Pathology: June 2011 - Volume 32 - Issue 2 - p 166-168
doi: 10.1097/PAF.0b013e318219c84c
Case Reports

We report the occurrence of a clinically undiagnosed biatrial myxoma with left ventricular involvement in a 2-month-old male infant, resulting in sudden death. During a routine well-baby examination, a grade (34) holosystolic murmur was detected at the left sternal border with radiation to the axilla and back. On the following day, the patient collapsed and died suddenly. An autopsy revealed a large multifocal neoplasm diffusely involving the aortic valve while displaying mitral, tricuspid, and left ventricular extensions. The ensuing histopathologic and immunohistochemical studies were diagnostic for myxoma. We discuss the occurrence of cardiac myxoma within the pediatric population and review the literature as to theorize whether this lesion was a congenital process versus a rapidly growing tumor that developed after the child was born. Lastly, we address the potential for sudden death in patients with such tumors.

From the *University of Missouri-Kansas City and Truman Medical Centers; and †Children's Mercy Hospital, Kansas City, MO.

Manuscript received April 29, 2008; accepted August 14, 2008.

Reprints: Daniel Lingamfelter, DO, Truman Medical Center, Pathology Department, 2301 Holmes St, Kansas City, MO 64108. E-mail:

© 2011 Lippincott Williams & Wilkins, Inc.