Pentalogy of Cantrell

Autor: Luis Alexis Arévalo-Salas, Norma Balderrabano-Saucedo, Erika Sandoval-Serrano, Begoña Segura-Stanford, Gonzalo Espinosa-Islas, Francisco Javier Puga-Muñuzuri, Lorenzo Reyes de la Cruz, Alfredo Vizcaíno-Alarcón
Rok vydání: 2011
Předmět:
Zdroj: World Journal for Pediatric and Congenital Heart Surgery. 2:211-218
ISSN: 2150-136X
2150-1351
DOI: 10.1177/2150135110390528
Popis: Pentalogy of Cantrell is a rare disease. Approximately 185 cases have been reported around the world. The authors performed a retrospective study that reviewed the clinical files and pathological samples of 22 cases of pentalogy of Cantrell treated at the Hospital Infantil de México Federico Gómez. Thirteen patients had ectopia cordis associated with pentalogy of Cantrell (group I), and there were 9 cases without ectopia cordis (group II). In group I, the following types of congenital heart disease were found: single ventricle (4), double-outlet right ventricle (4), ventricular septal defect (3), aortic coarctation (1), and atrial septal defect (1). In group II, the following types of congenital heart disease were found: double-outlet right ventricle (3), double-inlet left ventricle (2), ventricular septal defect (2), tetralogy of Fallot (1), and hypoplastic right ventricle syndrome (1). Nine cases had a ventricular diverticulum (40%). Ten patients (45%) had some other congenital anomaly associated with pentalogy of Cantrell. Thirteen patients underwent surgery (59%), which included cardiac surgery in 10 cases (45%). Sixteen patients died (73%): 11 from group I and 5 from group II ( P < .05). Little more than 50 years since it was first described, pentalogy of Cantrell remains a disease with high mortality, especially in patients with associated ectopia cordis.
Databáze: OpenAIRE
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