Abstract
A case of cardiac fibroma in a neonate with a fatal outcome due to consumptive coagulopathy is described. Fetal monitoring suggested a cardiac anomaly during labour, and the tumor was clinically manifest from birth with exceptionally wide anatomic spread.
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Edwards JE (1968) Heart disease in infants, children and adolescents. Moss AJ, Adams FH (eds) Williams and Wilkins, Baltimore, pp 1072–1073
Freeman JA, Geer JC, Randall WS, Palfrey WG (1963) Intramural fibroma of the heart. Am J Clin Pathol 39:374–381
Geha AS, Weidman WH, Soule EH, McGoon DC (1967) Intramural ventricular cardiac fibroma: Successful removal in two cases and review of the literature. Circulation 36:427–440
Griffiths GC (1965) A review of primary tumors of the heart. Progr Cardiovasc Dis 7:465–479
Nadas AS, Ellison RC (1968) Cardiac tumors in infancy. Am J Cardiol 21: 363–366
Simcha A, Wells BG, Tynan MJ, Waterston SJ (1971) Primary cardiac tumors in children. Arch Dis Child 46:508–514
Sugarman RG, Rawlinson KF, Schifrin BS (1978) Fetal arrhythmia. Obstet Gynecol 52:301–307
Turi GK, Albala A, Fengolio JJ (1980) Cardia Fibromatosis: An ultrastructural study. Hum Pathol 11:577–580
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Abend, M., Tirosh, E., Grishkan, A. et al. Congenital cardiac fibroma: An unusual presentation. Eur J Pediatr 139, 207–209 (1982). https://doi.org/10.1007/BF01377361
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DOI: https://doi.org/10.1007/BF01377361