ABSTRACT
Se presenta un caso de atresia de esófago en el que se practicó anastomosis primaria, cierre de fístula y gastrotomía sobreviviendo hasta la fecha, atribuyéndose el éxito a los cuidados pre y postoperatorios. Se hacen consideraciones acerca de esta malformación haciendo hincapié en los datos que se deben tener en cuenta para fundar el diagnóstico
Subject(s)
Humans , Male , Infant, Newborn , Anastomosis, Surgical , Esophageal Atresia/surgery , Esophageal Atresia/diagnosis , Esophageal Atresia/physiopathology , Esophagus/surgery , Esophagus/physiopathology , Tracheoesophageal Fistula/surgery , Pediatrics , MexicoABSTRACT
Se informa acerca de un caso de síndrome poliploide en un recién nacido con cariotipo 46 XY, el cual presentaba diversas malformaciones señaladas en los pocos casos que han aparecido en la literatura, presentando, además, atresia de esófago con fístula gastrobronquial
Subject(s)
Humans , Male , Infant, Newborn , Polyploidy , Sex Chromosome Aberrations/physiopathology , Sex Chromosome Aberrations/genetics , Abortion, Spontaneous , Esophageal Atresia/surgery , Esophageal Atresia/physiopathology , SyndromeABSTRACT
Retrospective study of 15 histories patient with esofagical atresia at Hospital Central of San Cristobal and Hospital Dr. Patrocinio Peñuela Ruíz from San Cristobal from 1983-1992. The mortality rate was 71 per cent to HCSC vs. 25 per cent HPPR. The incidence of EA was 1:2000 HCSC and 1:4000 HPPR. The diagnosis was be in all child by maneuver of passing a catheter down the esophagus, but very last 66 per cent after the first 12 hours. The 86 per cent of the infant are of the Type III variety. Haight anasthomosis was be in 14 cases win 100 per cent effectiveness. Emergency gastrotomy was in four cases. The definitive oration was delayed in one case., Esophagical anomalies present a chalenge to the pediatric surgeon and demmand close attention and care fron the nursins staff as well the surgical staff