(Circulation. 2000;101:e168.)
© 2000 American Heart Association, Inc.
Images in Cardiovascular Medicine |
From the Division of Pediatric Cardiology, Cedars-Sinai Medical Center and Department of Pediatrics, University of California (J.A.W.), and the Department of Pathology and Laboratory Medicine, University of California (M.C.F.), Los Angeles.
Correspondence to Jeffrey A. Wong, MD, Division of Pediatric Cardiology, 5400 Balboa Blvd, Suite 202, Encino, CA 91316. E-mail jwong{at}mailgate.csmc.edu
A previously well
and asymptomatic 6-year-old boy collapsed at school. He was
initially asystolic but was resuscitated to sinus rhythm. Then,
during transport to the hospital, he developed monomorphic
ventricular tachycardia (Figure 1
). Transthoracic
echocardiography demonstrated a huge,
homogeneous intramural mass in the left
ventricular free wall, possibly also involving the left
atrial wall, remarkably without evidence of ventricular
systolic dysfunction or left ventricular outflow
tract obstruction (Figure 2
). Despite
aggressive antiarrhythmic therapy, the patients cardiac rhythm
deteriorated further, and support was withdrawn after signs of
irreversible multisystem organ failure developed.
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Postmortem examination revealed a 7x4x4-cm, firm, well-demarcated
intramural mass in the posterior free wall of the left ventricle
(Figure 3
). Microscopic examination
revealed that the mass consisted primarily of fibrous tissue with focal
calcifications (not shown) infiltrating the adjacent
myocardium, consistent with a fibroma (Figure 4
).
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Footnotes
The editor of Images in Cardiovascular Medicine is Hugh A. McAllister, Jr, MD, Chief, Department of Pathology, St Lukes Episcopal Hospital and Texas Heart Institute, and Clinical Professor of Pathology, University of Texas Medical School and Baylor College of Medicine.
Circulation encourages readers to submit cardiovascular images to the Circulation Editorial Office, St Lukes Episcopal Hospital and Texas Heart Institute, 6720 Bertner Ave, MC1-267, Houston, TX 77030.
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