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Benign congenital cardiac tumor associated with a ‘malignant’ cardiac malformation

Published online by Cambridge University Press:  19 August 2008

Andrew M. Davis ,
Meredith M. Silver  and
Robert M. Freedom
Andrew M. Davis
Affiliation:
From the Division of Cardiology, Department of PaediatricsThe Hospital for Sick Children and University of Toronto, Toronto
Meredith M. Silver
Affiliation:
Department of Pathology, The Hospital for Sick Children and University of Toronto, Toronto
Robert M. Freedom*
Affiliation:
From the Division of Cardiology, Department of PaediatricsThe Hospital for Sick Children and University of Toronto, Toronto Department of Pathology, The Hospital for Sick Children and University of Toronto, Toronto
*
Dr. Robert M. Freedom, Director, Division of Cardiology, Department of Paediatrics, The Hospital for Sick Children, 555 University Avenue, Toronto, M5G 1X8, Ontario, Canada. Tel. 416-813-6132; Fax. 416-813-7547.
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Summary

We describe a multicystic tumor of the atrial septum associated with a fatal cardiac malformation. The tumor contained bronchogenic cysts and two types of vascular hamartomas. A complex form of double outlet right ventricle was present. We speculate that this tumor formed at a critical time in cardiac embryogenesis and contributed to the abnormal formation of the heart.

Keywords

Cardiac tumorbronchogenic cysthamartoma
Type
Brief Reports
Information
Cardiology in the Young , Volume 6 , Issue 1 , January 1996 , pp. 84 - 87
Copyright
Copyright © Cambridge University Press 1996

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References

1. Van dei Hauwaert, LG. Cardiac tumors in infancy and child hood. Br Heart J 1971; 33: 125–132.CrossRefGoogle Scholar
2. McAllister, HA, Fenoglio, JJ. Tumors of the cardiovascular system. In: Hartmann, WH (ed). Atlas of Tumor Pathology; vol Fascicle 15. Armed Forces Institute of Pathology, Washington, 1978.Google Scholar
3. Weinberg, PM. Fetal hydrops in a newborn with hypoplastic left heart syndrome: Tricuspid valve “stopper”. J Am Coll Cardiol 1985; 6: 1365–1369.Google Scholar
4. Kuijer, P, Dion, R, Van Merrienboer, F. Right atrial spleen. Br Heart J 1985: 54: 337–339.CrossRefGoogle ScholarPubMed
5. Meligrana, F, Sugar, L, Casella, L, Birnbaum, PL, Salerno, T. Succesful removal of an unusual cystic mass of the heart. Can J Cardiol 1994; 10: 555–558.Google Scholar
6. Thomas, R, Van Wesep, R. Intracardiac epithelial cyst in association with an atrioventricular canal defect. Am J Cardiovasc Path 1990; 3: 325–327.Google ScholarPubMed
7. Dabbs, CH, Berg, R, Peirce, EC. Intrapericardial bronchogenic cysts. J Thoracic Surg 1957; 34: 723–733.CrossRefGoogle ScholarPubMed
8. Swalwell, CI. Benign intracardiac teratoma: a case of sudden death. Arch Pathol Lab Med 1993; 117: 739–742.Google ScholarPubMed
9. Rose, AC. Venous malformations of the heart. Arch Pathol Lab Med 1979; 103: 18–20.Google ScholarPubMed
10. Russell, GA. Coexistant cardiac tumors and malformations of the heart. Int J of Cardiol 1989; 22: 89–98.CrossRefGoogle ScholarPubMed