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Perinatal intracardiac teratoma: unusual presentation and review of the literature

Published online by Cambridge University Press:  08 February 2019

Anne Moreau de Bellaing
Affiliation:
M3C-Necker, Hôpital Necker-Enfants malades, AP-HP, Paris, France Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Lucile Houyel
Affiliation:
Hôpital Marie-Lannelongue, Le Plessis-Robinson, France
Damien Bonnet
Affiliation:
M3C-Necker, Hôpital Necker-Enfants malades, AP-HP, Paris, France Université Paris Descartes, Sorbonne Paris Cité, Paris, France

Abstract

Intracardiac teratomas are rare primary tumours. We report the case of an infant prenatally diagnosed with an isolated multi-cystic mass developed in the right ventricle causing neonatal refractory ventricular arrhythmia. Despite rescue extracorporeal support and partial surgical resection, he died as almost all the previous reported perinatal intracardiac teratomas whatever the prenatal tolerance and the size of the tumour. The common poor outcome of fetal intracardiac teratomas should be known when counselling parents during pregnancy.

Type
Brief Report
Copyright
© Cambridge University Press 2019 

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Footnotes

Cite this article: Moreau de Bellaing A, Houyel L, Bonnet D (2019). Perinatal intracardiac teratoma: unusual presentation and review of the literature. Cardiology in the Young29: 439–441. doi: 10.1017/S1047951118002354

References

1. Uzun, O, Wilson, DG, Vujanic, GM, Parsons, JM, De Giovanni, JV. Cardiac tumours in children. Orphanet J Rare Dis 2007 Mar 1; 2: 11.Google Scholar
2. Campagne, G, Quereda, F, Merino, G, et al. Benign intracardiac teratoma detected prenatally. Case report and review of the literature. Eur J Obstet Gynecol Reprod Biol 1998; 80: 105108.Google Scholar
3. Gembicki, M, Hartge, DR, Hoffmann, U, Krapp, M, Vokuhl, C, Weichert, J. Severe obstruction of the fetal right ventricular outflow tract due to a primary teratoma originating from the interventricular septum and resulting in neonatal death. J Ultrasound Med 2016; 35: 663667.Google Scholar
4. Ou, P, Dorrière, V, Sidi, D, Bonnet, D, Vouhé, P. Images in cardiovascular medicine. Cardiac teratoma in a newborn with right ventricular outflow tract obstruction. Circulation 2006; 113: e17e18.Google Scholar
5. Stiller, B, Hetzer, R, Meyer, R, et al. Primary cardiac tumours: when is surgery necessary? Eur J Cardiothorac Surg 2001; 20: 10021006.Google Scholar
6. Williams, GE. Teratoma of the heart. J Pathol Bacteriol 1961; 82: 281285.Google Scholar
7. Van der Hauwaert, LG. Cardiac tumours in infancy and childhood. Br Heart J 1971; 33: 125132.Google Scholar
8. Costas, C, Williams, RL, Fortune, RL. Intracardiac teratoma in an infant. Pediatr Cardiol 1986; 7: 179181.Google Scholar
9. Farooki, ZQ, Chang, CH, Jackson, WL, et al. Intracardiac teratoma in a newborn. Clin Cardiol 1988; 11: 642644.Google Scholar
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