Intestinal atresia is any congenital malformation of the structure of the intestine that causes bowel obstruction. The malformation can be a narrowing (stenosis), absence or malrotation of a portion of the intestine. These defects can either occur in the small or large intestine.
Symptoms and signs The most prominent symptom of intestinal atresia is bilious vomiting soon after birth. This is most common in jejunal atresia. Other features include abdominal distension and failure to pass meconium. The distension is more generalised the further down the bowel the atresia is located and is thus most prominent with ileal atresia. Inability to pass stool is most common with duodenal or jejunal atresia; if stool is passed, it may be small, mucus-like and grey. Occasionally, there may be jaundice, which is most common in jejunal atresia. Abdominal tenderness or an abdominal mass are not generally seen as symptoms of intestinal atresia. Rather, abdominal tenderness is a symptom of the late complication meconium peritonitis. Before birth, excess amniotic fluid (polyhydramnios) is a possible symptom. This is more common in duodenal and oesophageal atresia.
Cause The most common cause of non-duodenal intestinal atresia is a vascular accident in utero that leads to decreased intestinal perfusion and ischemia of the respective segment of bowel. This leads to narrowing, or in the most severe cases, complete obliteration of the intestinal lumen. In the case that the superior mesenteric artery, or another major intestinal artery, is occluded, large segments of bowel can be entirely underdeveloped (Type III). Classically, the affected area of bowel assumes a spiral configuration and is described to have an "apple peel" like appearance; this is accompanied by lack of a dorsal mesentery (Type IIIb). An inherited form – familial multiple intestinal atresia – has also been described. This disorder was first reported in 1971. It is due to a mutation in the gene TTC7A on short arm of chromosome 2 (2p16). It is inherited as an autosomal recessive gene and is usually fatal in infancy. Ileal atresia can also result as a complication of meconium ileus. A third of infants with intestinal atresia are born prematurely or with low birth weight.
Diagnosis Intestinal atresias are often discovered before birth; either during a routine sonogram which shows a dilated intestinal segment due to the blockage, or by the development of polyhydramnios (the buildup of too much amniotic fluid in the uterus). These abnormalities are indications that the fetus may have a bowel obstruction which a more detailed ultrasound study can confirm. Infants with stenosis instead of atresia are often not discovered until several days after birth. Some fetuses with bowel obstruction have abnormal chromosomes. An amniocentesis is recommended because it can determine not only the sex of the baby, but whether or not there is a problem with the chromosomes. If not diagnosed in utero, infants with intestinal atresia are typically diagnosed at day 1 or day 2 after presenting with eating problems, vomiting, and/or failure to have a bowel movement. Diagnosis can be confirmed with an X-ray, and typically followed with an upper gastrointestinal series, lower gastrointestinal series, and ultrasound.
Classification
By location Intestinal atresia may be classified by its location. Patients may have intestinal atresia in multiple locations.
Duodenal atresia – malformation of the duodenum, part of the intestine that empties from the stomach, and first section of the small intestine Jejunal atresia – malformation of the jejunum, the second part of the small intestine extending from the duodenum to the ileum, that causes the jejunum to block blood flow to the colon Ileal atresia – malformation of the ileum, the lower part of the small intestine Colon atresia – malformation of the colon Malformations may also occur along multiple portions of the intestinal tract; for instance a malformation that occurs along or spans the length of the jejunum and the ileum is termed jejunoileal atresia.
By malformation Intestinal atresia can also by classified by the type of malformation. The classification system by Bland-Sutton and Louw and Barnard (1955) initially divided them into three types. This was later expanded to five by Zerella and Grosfeld et al.
Type I In type I, there is a wall (septum) or membrane at some point in the bowel, leading to dilation of the bowel on the nearer side and a collapse of the bowel on the latter side. Bowel length is not usually affected in this type.
Type II In type II, there is a gap in the bowel, and either end of the remaining intestine is closed off and connected to the other by a fibrous cord that runs along the edge of the mesentery. The mesentery remains intact.
Type IIIa Type IIIa is similar to type II, but the mesentery is defective (there is a V-shaped gap), and the bowel length may be shortened.
Type IIIb In type IIIb, also known as the "apple peel" or "Christmas tree" deformity, the atresia affects the jejunum, and the intestine is often malrotated with most of the mesenteric arteries absent. The remaining ileum, which is of varying length, survives on a single mesenteric artery, which it is twisted around in a spiral form. The term apple-peel intestinal atresia is generally reserved for when it affects the jejunum, while Christmas tree intestinal atresia is used if it affects the duodenum. It may affect both, however.
Type IV Type IV involves a combination of all the other types and takes the appearance of a string of sausages. The length of the bowel is always shortened, but the last part of the ileum is usually not affected, as in type III. This type usually affects the nearest end of the jejunum, but the far end of the ileum may instead be affected.
Treatment Fetal and neonatal intestinal atresia are treated using laparotomy after birth. If the area affected is small, the surgeon may be able to remove the damaged portion and join the intestine back together. In instances where the narrowing is longer, or the area is damaged and cannot be used for period of time, a temporary stoma may be placed. The infant is usually given intravenous fluid hydration, and a nasogastric or orogastric tube may be used to aspirate the contents of the stomach. The nutritional administration is maintained after surgery until the bowel can resume normal function.
Prognosis
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