Congenital Ileal Atresia in Newborn.
10.12701/yujm.1994.11.1.35
- Author:
Young Soo HEO
;
Chang Sig KIM
;
Son Moon SHIN
- Publication Type:Original Article
- MeSH:
Abdomen;
Diagnosis;
Female;
Gestational Age;
Humans;
Infant, Newborn*;
Male;
Meconium;
Postoperative Complications;
Vomiting
- From:Yeungnam University Journal of Medicine
1994;11(1):35-41
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Newborns with ileal atresia frequently present with abdominal distension, bilious vomiting, and failure to pass meconium. Diagnosis is usually established on plain x-ray of the abdomen by the findings of distended small bowel loops and air-fluid levels. In the period of October 1988 to February 1994, 8 patients with congenital ileal atresia were operated and the following results were obtained. 1. Eight patients were comprise of 4 males and 4 females, the ratio of male and female was 1 : 1. 2. Six patients(75%) had been admitted to our hospital during three days of life. 3. Congenital ileal atresia was in 8 cases : Type I in two(25%), Type II in two(25%), Type III a in three(37.5%), Type III b in one(12.5%). 4. There was one premature patient who was small for gestational age. 5. Overall, abdominal distension and bilious vomiting occurring in seven patients, were frequent presenting complaints. 6. Diagnosis was possible with clinical symptom and simple abdomen. 7. Operative treatment was undertaken as soon as the diagnosis was made. In seven cases a primary end-to-end anastomosis was performed after resection of dilated proximal loop. 8. A total of four associated congenital anomalies were found in one patient. 9. Postoperative complications occurred in three cases(37.5%).
