Because your childs intestine is blocked by the atresia, a thin flexible tube will be inserted into your baby. Presentation and outcome of treatment of jejunoileal atresia in. Intestinal atresia can be caused by a problem with the blood supply to the intestines, such as a blood clot, during development. Jejunal atresia genetic and rare diseases information center. The baby becomes cyanotic on breastfeeding, and pink when crying. Intestinal atresia american pediatric surgical association. Clinic of pediatric surgery, university clinical center sarajevo, sarajevo, bosnia and herzegovina. Both types of atresia were repaired with primary handsewn. After the baby is born, small bowel atresia is usually diagnosed when there are signs of an obstruction, such as vomiting, green bile and a swollen abdomen. Isolated ascites in a newborn with apple peel jejunal. It causes increased levels of amniotic fluid during pregnancy polyhydramnios and intestinal obstruction in newborn babies.
Bile ducts are pathways that carry a digestive fluid called bile from the liver to the small intestine. Type i a mucosal septal, type ii a fibrous cordband, type iii blind ends are entirely separated without a fibrous cord between them and a large mesenteric defect, and type iv combination of atresia type i to iii. Ileal atresia happens in the last portion of the small intestine, just before the large intestine. Intestine atresia an overview sciencedirect topics. One neonate with jejunal atresia died of complications of extreme.
The atresias typically involve the shortest, widest part of the small intestine that joins the stomach duodenumone of the three portions of the small intestine that connects with the duodenum jejunumor the portion of the small intestine that opens into the large intestine ileumand the rectum. Occasionally, doctors may suggest using a contrast scan andor enema instead or as well as an xray. Biliary atresia is a rare disease of the bile ducts that affects only infants. Type iiib atresia 19% apple peel consists of a proximal jejunal atresia, often with malrotation with absence of most of the mesentery and a varying length of ileum surviving on perfusion from retrograde flow along a single artery of supply. Intestinal obstruction in neonatalpediatric surgery. Also see overview of congenital gastrointestinal anomalies. In this condition, because of agenesis of the mesentery, the distal small bowel comes straight off the caecum and twists around the marginal artery, suggesting a maypole, a christmas tree, or an apple peel at operation. Jejunal atresia happens in the midsection of the small intestine.
Resection of the blind ends was done and endtoend anastomosis was performed. Newborns with anal atresia usually present with such signs of lower intestinal obstruction as failure to pass meconium and abdominal distention. A very rare case of intestinal atresia, the apple peel syndrome. On day two of life, the baby developed bilious aspirates and an abdominal radiograph suggested intestinal obstruction. The most prominent symptom of intestinal atresia is bilious vomiting soon after birth. The underlying cause of jejunal and ileal atresias is an intrauterine ischemic insult, which can be a primary vascular cause or secondary to a volvulus. Congenital duodenal atresia and stenosis is a frequent cause of intestinal obstruction and occurs in 1 per 5000 to 10,000 live births, affecting boys more commonly than girls. Intestinal atresia is a congenital obstruction of the intestine, sometimes associated with a loss of tissue, resulting in a disruption of intestinal continuity. Intestinal atresia and duodenal atresia intestinal atresia absence of a normal opening is the failure of a portion of the intestinal tract to completely form.
Case report the combination of gastroschisis, jejunal atresia, and colonic atresia in a newborn zacharybauman 1 andvictornanagasjr. Intrauterine, intusussceptum, jejunal atresia, newborn. Jejunal atresia is a birth defect in a newborn characterized by partial or complete absence of the membrane connecting the small intestines to the abdominal wall the mesentery. Most blockages occur in the small intestine known as jejunal atresia, or ileal atresia but may also occur in the large intestine colonic atresia. Described for the first time in 1683 1 jejunoileal atresia is among the most. As a result, a portion of the small intestine the jejunal twists about one of the arteries to the colon. Cases with duodenal atresia were excluded from the search and subsequent analysis. At laparotomy, an apple peel jejunal atresia, abnormal mesentery with precarious blood supply and a proximal perforation were identified and the perforation sewn over. Duodenal atresia results in a blockage atresia that stops food or fluid from leaving the baby s stomach. Fifty percent of intestinal atresias occur in the jejunum or ileum. Duodenal atresia is a congenital present at birth intestinal obstruction in the form of complete obliteration of the duodenal lumen that can cause bilious or nonbilious vomiting within the first 24 to 38 hours of neonatal life. Chapter 63 intestinal atresia and stenosis alastair j. Type iv atresia is a multiple atresia of types i, ii, and iii, like a string of.
In conclusion, jejunal atresia mostly occurs in the proximal. Duodenal and intestinal atresia and stenosis clinical gate. Accuracy of prenatal ultrasound in detecting jejunal and. Intestinal obstruction is the common surgical problem in neonates of which intestinal atresia and stenosis contributes one third of cases. Intestinal obstruction in neonatalpediatric surgery by c. Duodenal and jejunal atresia with agenesis of the dorsal mesentery. It causes a portion of the small intestines the jejunum to twist around an artery that supplies blood to the colon the marginal artery. Get my notes in pdf files that are downloadable at s. This information is neither intended nor implied to be a substitute for professional medical advice. Jejunal atresia nord national organization for rare.
We identified all neonates with surgically confirmed jejunal or ileal atresia that had. The distension is more generalised the further down the bowel the atresia is located and is thus most prominent with ileal atresia. Gosche kokila lakhoo introduction atresias of the jejunum and ileum are common causes of bowel obstruction in the neonate, with a third of infants born prematurely or small for their gestational age. Neonates with jejunoileal atresia usually present late during day 1 or on day 2 with increasing abdominal distention, failure to. Neonatal intramural calcification in jejunal atresia. Atresias of the jejunum and ileum are common causes of bowel obstruction in the neonate, with a third of infants born prematurely or small for their gestational age. Inability to pass stool is most common with duodenal. Small bowel atresia, also known as intestinal atresia, is a birth defect that affects a part of the small intestine, the tube that connects the stomach to the large intestine and helps digest food. Jejunal atresia is one of several types of intestinal atresia but it is very uncommon. Sg 10 day old baby girl, born at 30 weeks gestation. Jejunoileal atresia merck manuals professional edition. The combination of gastroschisis, jejunal atresia, and colonic atresia in a newborn. Associated extraintestinal anomalies, including gastroschisis, intrauterine volvulus, and meconium ileus, are infrequent occurring in 7% of cases dalla vecchia et al, 1998.
Get a printable copy pdf file of the complete article 2. Jejunoileal obstruction was found in 46% of the intestinal atresias. Radiography shows a distended stomach and distended duodenum, which are separated by the pyloric valve, a finding described as the doublebubble sign. Hajivassiliou glasgow, scotland, uk intestinal obstruction in the newborn infant and older child may be due to a variety of conditions, including atresia and stenosis, annular pancreas, malrotation, duplication cyst, meconium ileus, meconium plug syndrome and neonatal. In general, intestinal atresia refers to atresias of the small intestine jejunum and ileum.
Intestinal atresia and stenosis usually involve the small intestine, but can affect any part of the gastrointestinal tract. A collection of disease information resources and questions answered by our genetic and rare diseases information specialists for jejunal atresia. We identified all neonates with surgically confirmed jejunal or ileal atresia that had prena tal sonography and neonatal surgery in our center from january 1, 1995. Duodenal atresia is the congenital absence or complete closure of a portion of the lumen of the duodenum. Histomorphological features of intestinal atresia and its. It was about a 4dayold male newborn who was admitted for a. Intestinal atresia is a narrowing, blockage, or absence of a portion of the small or large intestine in an infant before they are born. Normally, the lumen opening of the duodenum remains open during fetal development. Pdf intestinal atresias are a common cause of bowel obstruction in newborns. Intestinal obstruction in newborns maria georgiades, md august 4, 2011.
Jejunal atresia and stenosis obstruction of the jejunum is virtually always due to atresia or stenosis in neonates. Hajivassiliou glasgow, scotland, uk intestinal obstruction in the newborn infant and older child may be due to a variety of conditions, including atresia and stenosis, annular pancreas, malrotation, duplication cyst, meconium ileus, meconium plug. Jejunal atresia genetic and rare diseases information. The lumen of the distal segment contained an intussusceptum. Here, we report a case of a preterm newborn with fetal peritonitis, jejunal atresia with volvulus of postatresic small bowel since about 30 cm from ileocecal valve icv followed by a notused. Only studies reporting a prospective diagnosis of ndsba at the time of the examination or studies in. It causes a portion of the small intestines the jejunum to twist around an.
Most babies with intestinal atresia are comfortable breathing on their own, but your baby will be unable to nurse or take a bottle and will be fed nutrients intravenously instead. Resection and primary anastomosis of the jejunum and ileum in the newborn. Although the diagnosis of anal atresia can be made on the basis of physical examination alone, abdominal radiography can be useful for determining whether the infant has a high or low anal atresia. Other features include abdominal distension and failure to pass meconium. View the article pdf and any associated supplements and figures for. We encountered a rare case of gastroschisis associated with jejunal atresia and colonic atresia. Duodenal atresia happens in the first portion of the small intestine. Jejunal atresia jejunoileal atresia is incomplete formation of part of the small intestine.
Jejunal atresia associated with idiopathic ileal perforation. This study aims to elaborate jejunal atresia in the newborn after resection and. Jejunal atresia is a birth defect in which the fold of the stomach membrane needed to connect the small intestine to the back wall of the abdomen is, in part, absent. Duodenal atresia causes, symptoms, diagnosis, treatment. In our case, the jejunal atresia was not discovered for 27 days after the initial abdominal wall closure. Jejunoileal small bowel atresia is a common cause of neonatal intestinal.
Carol lynn berseth, dan poenaru, in averys diseases of the newborn eighth edition, 2005. Newborn female infant with abdominal distension and failure to pass stool. Intestinal stenosis is a partial obstruction that causes the center opening of the intestine to become narrower, while intestinal atresia is a complete closure of the intestine. Jejunal atresia is the most common cause of bowel obstruction in the newborn. Newborns who are found to have another condition that can cooccur with atresia, such as cystic fibrosis or malabsorption syndromes, may need additional, specialized care. Bowel obstruction in the newborn is one of the most common surgical problems, and its successful management depends upon both timely diagnosis and. Jejunoileal atresias and stenoses are major causes of neonatal intestinal obstruction. Duodenal atresia is a rare congenital present at birth condition involving the first part of the small intestine called the duodenum.
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