2015, Number 1
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Rev Cubana Pediatr 2015; 87 (1)
Cardiac rhabdomyoma
Céspedes AM, Suzarte PJ, Mansito GN
Language: Spanish
References: 12
Page: 102-108
PDF size: 181.19 Kb.
ABSTRACT
Rhabdomyoma is a primary cardiac benign tumor. This report described a 4 days-old
newborn born to eutocic delivery at 40 weeks of gestational age and good
birthweight. He was born through transpelvic route with no perinatal morbidity, Apgar
test of 9/9, but few hours after birth, he was detected an intensity II/IV cardiac
murmur with no other clinical signs. The echocardiographic results showed pedicled
tumor mass with obstructive characteristics of the outlet tract of the left ventricle, thus generating around 80 mmHg gradient at that level. This wide-base, pearly and
flat surface tumor was excised by means of oblique aortotomy using extracorporeal
circulation. The postoperative phase was uncomplicated. The patient recovers with
neither residues nor sequelae after 12 months of follow/up.
REFERENCES
Moran A, Gerald M. Cardiactumors. In: Allen HD, Driscoll DJ, Shaddy RE, Feltes TF, editors. Moss And Adams Heart Disease in Infants, children and adolescents: Including the Fetus and Young Adults. Philadelphia: Lippincott Williams & Wilkins; 2008. p. 1479-95.
Uzun O, Wilson D, Vujanic G, Parson J. Cardiac tumours in children. Orphanet Journal of Rare Diseases. 2007;2(11):44-56.
Kohut J, Krzystolik-ładzińska J, Szydłowski L, Smoleńska-petelenz J, Giec-fuglewicz G, Pająk J. The diagnosis, clinical course and follow-up of children with cardiac tumours -a single-centre experience. Kardiologia Polska. 2010;68:304-9.
Chávez IM, Castellanos LM, Hernández AB, Faustro AA, Orellana JE, Marroquín SR. Rabdomioma gigante intracardíaco en la etapa neonatal. Reporte de un caso. Arch Cardiol Méx. 2004;74(1):49-52.
Pruksanusak N, Suntharasaj T, Suwanrath C, Phukaoloum M. Fetal Cardiac Rhabdomyoma with Hydrops Fetalis. JUM. 2012;31(11):1821-4.
López JÁC, Jiménez YG, Gutiérrez LY, Arteaga SJ, Sánchez AM, Cardeña JO, et al. Rabdomioma cardiaco tratado quirúrgicamente con éxito y revisión de la literatura. Arch Cardiol Méx. 2005;75(3):22-4.
Chao AS, Chao A, Wang HT, Chang CY, Hsieh CC, Lien R, et al. Outcome of antenatally diagnosed cardiac rhabdomyoma case series and a meta-analysis. Ultrasound in Obstetrics & Gynecology. 2008;31(3):289-95.
De Rosa G, Carolis M, Pardeo M, Bersani I. Neonatal emergencies associated with cardiac rhabdomyomas: an 8-year experience. Fetal Diagn. 2011;29(2):169-77.
Khatare P, Muthuswamy K, Sadasivan J, Calumbar N. Incessant ventricular tachycardia due to multiple cardiac rhabdomyomas in an infant with Tuberous Sclerosis. Indian Heart J. Jan 2013;65(1):111-3.
Yadava OP. Cardiac tumours in infancy. Indian Heart J. 2012;64(5):492-6.
Neri M, Di Donato S, Maglietta R, Pomara C. Sudden death as presenting symptom caused by cardiac primary multicentric left ventricle rhabdomyoma, in an 11-month-old baby. An immunohistochemical study. Diagn Pathol. 2012;7:169.
Bédard E, Becker AE, AGatzoulis M. Cardiac Tumours. In: Kennedy JF, Suite B, Cardiology P, Livingstone C, editors. Paediatric Cardiology. Philadelphia: Elsevier; 2010. p. 1055-65.