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1.
Article in English | IMSEAR | ID: sea-43018

ABSTRACT

BACKGROUND: Atresia of the jejunum and ileum is one of the major causes of neonatal intestinal obstruction. Most affected newborn infants present with bilious emesis and abdominal distention. Traditionally, jejunal and ileal atresia have been grouped together as jejunoileal atresia. OBJECTIVE: To elucidate the difference between jejunal and ileal atresia. MATERIAL AND METHOD: A retrospective analysis of patients diagnosed with jejunal or ileal atresia, who were treated at the Department of Surgery, Queen Sirikit National Institute of Child Health during January 1988 to December 2007, was carried out. RESULTS: There were 74 patients with jejunal atresia and 68 patients with ileal atresia. The mean birth weight and gestational age of patients with jejunal atresia were significantly lower than those with ileal atresia. Antenatal perforation occurred more frequently in ileal atresia. Postoperative course was more prolonged and mortality was higher injejunal atresia. Prolonged ileus and anastomotic dysfunction requiring long-term parenteral nutrition were the major causes of complications leading to death. CONCLUSION: There were many differences between patients with jejunal atresia and those with ileal atresia. The more compliant jejunal wall allows massive dilatation upon obstruction with subsequent loss of peristaltic activity, thus poorer outcome in comparison with ileal obstruction. We suggest that atresia of the jejunum and ileum be considered differently.


Subject(s)
Female , Humans , Ileum/abnormalities , Infant , Infant, Newborn , Intestinal Atresia/diagnosis , Jejunum/abnormalities , Male , Retrospective Studies
2.
Article in English | IMSEAR | ID: sea-42675

ABSTRACT

Epigastric heteropagus twins (EHT) is a rare form of conjoined twins. It refers to unequal and asymmetric conjoined twins in which the dependent part (parasite) is attached to the epigastrium of the dominant part (autosite). The authors herein report four cases of EHT. Omphalocele was present in 3 patients. Surgical excision of the parasite and repair of the abdominal wall defect were successful in three cases. Three infants had associated cardiac anomalies and one of them died during surgery from cardiopulmonary failure.


Subject(s)
Abnormalities, Multiple , Fatal Outcome , Female , Humans , Infant, Newborn , Male
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