Imaging in Duodenal Atresia

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Imaging in Duodenal Atresia

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Duodenal atresia represents complete obliteration of the duodenal lumen (see the images below). A duodenal diaphragm (or duodenal web) is thought to represent a mild form of atresia. Duodenal stenosis (incomplete obstruction of the duodenal lumen) is discussed with duodenal atresia because the 2 disorders together represent a spectrum of similar intrauterine events.

The incidence of duodenal atresia is 1 per 6000 births in the United States. Intrinsic congenital duodenal obstruction constitutes two thirds of all congenital duodenal obstructions (duodenal atresia, 40-60%; duodenal web, 35-45%; annular pancreas, 10-30%; duodenal stenosis, 7-20%). There is no racial predilection, and the incidence of duodenal atresia and duodenal stenosis is approximately equal in males and females.

One half of the neonates with duodenal atresia or stenosis are born prematurely, and hydramnios occurs in approximately 40% of neonates with duodenal obstruction. In addition, duodenal atresia or duodenal stenosis is most commonly associated with trisomy 21 (see the following image): about 22-30% of patients with duodenal obstruction have trisomy 21.

In most cases, duodenal atresia occurs below the ampulla of Vater. In a very few cases, the atresia occurs proximal to the ampulla. Annular pancreas occurs when pancreatic tissue surrounds the second portion of the duodenum. If the encirclement is complete, it may be associated with complete or incomplete duodenal obstruction. Because duodenal atresia or duodenal stenosis occurs in all cases of annular pancreas, the anomalous pancreas should be considered a secondary change rather than a primary cause of duodenal obstruction.

Plain radiographs that demonstrate a double-bubble appearance with no distal gas are characteristic of duodenal atresia (see the images below). Distal bowel gas indicates stenosis, incomplete membrane, or a hepatopancreatic ductal anomaly. Occasionally, a radiograph must be obtained with the patient in the erect or the decubitus position to delineate the duodenal component. If a combination of esophageal atresia and duodenal atresia is present, ultrasonography is preferred. [1]

No oral contrast materials are necessary in the evaluation of complete duodenal obstruction. Occasionally, a small amount of positive contrast material can be instilled through a feeding tube into the distal stomach and duodenum to differentiate the diaphragm from a long stenosis.

Occasionally, barium enema examination is suggested as an adjunct study in the evaluation of duodenal atresia (see the image below). Barium enema findings can demonstrate a malpositioned cecum, but this is not always diagnostic of malrotation and volvulus. In addition, if a microcolon is demonstrated, the presence of additional, more distal atresias can be suggested. Succus entericus may be prevented from reaching the colon because of the additional area of bowel obstruction. Multiple atresias are present in approximately 15% of patients. However, most surgeons can determine the presence of malrotation and additional atresias at the time of surgery. [2]

To the author’s knowledge, in only 1 instance was the addition of the barium enema examination beneficial to the preoperative examination of a patient with trisomy 21. This case involved the coexistence of Hirschsprung disease. (The presence of trisomy 21 makes the likelihood of Hirschsprung disease in a patient 15-fold greater.) If these conditions are known before surgery, the surgeon can create a temporizing colostomy at the time of duodenojejunostomy and spare the child from undergoing additional anesthesia.

Duodenal atresia or duodenal stenosis can be associated with other gastrointestinal and biliary tract abnormalities (malrotation, esophageal atresia, ectopic anus, annular pancreas, gallbladder or biliary atresia, vertebral anomalies). Sandrasegaran et al reviewed the records of 42 adults with annular pancreas who underwent endoscopic retrograde cholangiopancreatography (ERCP), computed tomography (CT) scanning, and magnetic resonance imaging (MRI) evaluations to determine whether annular pancreas can be diagnosed without radiologic findings of a complete ring of pancreatic tissue and found of 24 patients who had CT scan or MRI findings of annular pancreas, 9 had a radiologically incomplete ring of pancreatic tissue surrounding the second part of the duodenum. [3] Three the 9 patients had gastric outlet obstruction, and 6 of 15 patients with complete annular pancreas were also found to have gastric outlet obstruction.

The study demonstrated a 92% sensitivity and 100% specificity for annular pancreas when pancreatic tissue was present posterolateral to the second part of the duodenum. [3] In addition, there was a 37% rate of pancreatic divisum and a 48% rate of chronic pancreatitis. Sandrasegaran et al also observed that a crocodile jaw configuration of pancreatic tissue was suggestive of annular pancreas. [3]

Duodenal atresia can also be associated with a duodenal diaphragm, as well as with congenital abnormalities in other systems. Examples include VATER (vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, radial and renal anomalies) association and VACTERL (vertebral, anal, cardiac, tracheal, esophageal, renal, limb) syndrome. [4, 5, 6]

Anomalies of the kidneys can occur in VATER association; the most common of these renal abnormalities include aplasia, dysplasia, hydronephrosis, ectopia, persistent urachus, vesicoureteral reflux, and ureteropelvic obstruction.

Ruptured abdominal aortic aneurysm and midgut volvulus are considered in the differential diagnosis of duodenal atresia and duodenal stenosis. In addition, other conditions to be considered include a preduodenal portal vein, Ladd bands, duplication of the duodenum, tumor or hematoma of the duodenum, and a retroperitoneal tumor.

The double-bubble sign represents dilatation of the stomach and duodenum (see the images below). This configuration most commonly occurs with duodenal atresia and an annular pancreas. An annular pancreas is almost always associated with duodenal atresia.

In a few cases of duodenal atresia, air can be observed distal to the area of obstruction. The anomalous hepatopancreatic ducts permit movement of air through a Y-shaped ductal system, with 1 limb proximal to the obstruction and 1 limb distal to the atresia (see the following image).

When duodenal atresia is combined with esophageal atresia, no air is observed in the stomach. Because the stomach is obstructed at both ends, the infant presents with a large, opaque upper midabdominal mass. If esophageal atresia exists along with a distal fistula, air is found in the stomach and duodenum.

Duodenal obstruction in the neonate may be partial or complete, and it may be secondary to intrinsic or extrinsic abnormalities. The duodenal bulb may be larger in duodenal atresia than in obstructions of the duodenum. Increased intramural pressure in duodenal obstruction can result in gastric pneumatosis.

Once the radiographic finding of a double-bubble sign without distal gas is determined, the diagnosis of duodenal atresia is evident, and usually, no additional, contrast-enhanced studies are needed.

Duodenal atresia that is associated with a Y-shaped biliary duct connection can have air distal to the point of duodenal atresia. This finding may suggest stenosis rather than atresia (see the following image).

Cronin et al retrospectively assessed the role of a magnetic resonance small-bowel follow-through (MR SBFT) for small-bowel pathology in 17 children and found that MR SBFT allows pseudodynamic functional imaging and identifies extraluminal disease without biologic risk. [7] MR SBFT advantages included high tolerability (84.2%), lack of ionizing radiation, avoidance of duodenojejunal intubation, and excellent achievement of luminal distention. Pathologic lesions were identified in 53% of cases. In addition, there was high interobserver agreement regarding mean distention scores; the MR table time was short, without any early termination; there were few visits to the MR table; and the mean duration for complete small-bowel evaluation was 25 minutes.

A finding of 2 echo-free fluid collections in the upper abdomen suggests duodenal atresia in association with esophageal atresia. Esophageal atresia without a fistula does not permit air to reach the stomach and duodenum. [8] These findings do not require confirmation with additional procedures.

Kadian YS, Rattan KN. Congenital Pyloric Atresia with Distal Duodenal Atresia- Role of CT Scan. J Neonatal Surg. 2014 Jul-Sep. 3 (3):37. [Medline].

Parmentier B, Peycelon M, Muller CO, El Ghoneimi A, Bonnard A. Laparoscopic management of congenital duodenal atresia or stenosis: A single-center early experience. J Pediatr Surg. 2015 May 28. [Medline].

Sandrasegaran K, Patel A, Fogel EL, Zyromski NJ, Pitt HA. Annular pancreas in adults. AJR Am J Roentgenol. 2009 Aug. 193(2):455-60. [Medline].

Stark Z, Patel N, Clarnette T, et al. Triad of tracheoesophageal fistula-esophageal atresia, pulmonary hypoplasia, and duodenal atresia. J Pediatr Surg. 2007 Jun. 42(6):1146-8. [Medline].

Shaw-Smith C. Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: Roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature. Eur J Med Genet. 2009 Oct 13. [Medline]. [Full Text].

Choudhry MS, Rahman N, Boyd P, Lakhoo K. Duodenal atresia: associated anomalies, prenatal diagnosis and outcome. Pediatr Surg Int. 2009 Aug. 25(8):727-30. [Medline].

Cronin CG, Lohan DG, Browne AM, et al. MR small-bowel follow-through for investigation of suspected pediatric small-bowel pathology. AJR Am J Roentgenol. 2009 May. 192(5):1239-45. [Medline].

Hayden CK Jr, Schwartz MZ, Davis M, et al. Combined esophageal and duodenal atresia: sonographic findings. AJR Am J Roentgenol. 1983 Feb. 140(2):225-6. [Medline].

Kassner EG, Sutton AL, De Groot TJ. Bile duct anomalies associated with duodenal atresia; paradoxical presence of small bowel gas. Am J Roentgenol Radium Ther Nucl Med. 1972 Nov. 116(3):577-83. [Medline].

Kataria R, Bhatnagar V, Wadhwa S, et al. Gastric pneumatosis associated with preduodenal portal vein, duodenal atresia, and asplenia. Pediatr Surg Int. 1998 Nov. 14(1-2):100-1. [Medline].

Knechtle SJ, Filston HC. Anomalous biliary ducts associated with duodenal atresia. J Pediatr Surg. 1990 Dec. 25(12):1266-9. [Medline].

McCook TA, Felman AH. Esophageal atresia, duodenal atresia, and gastric distention: report of two cases. AJR Am J Roentgenol. 1978 Jul. 131(1):167-8. [Medline].

Robinson AE, Grossman H, Brumley GW. Pneumatosis intestinals in the neonate. Am J Roentgenol Radium Ther Nucl Med. 1974 Feb. 120(2):333-41. [Medline].

Ueki T, Yao T, Beppu T, et al. Three-dimensional computed tomography pancreatography of an annular pancreas with special reference to embryogenesis. Pancreas. 2006 May. 32(4):426-9. [Medline].

Gerald Mandell, MD, FACR, FAAP, FACNM Chief of Nuclear Medicine, Department of Radiology, Phoenix Children’s Hospital

Gerald Mandell, MD, FACR, FAAP, FACNM is a member of the following medical societies: American Academy of Pediatrics, American College of Nuclear Physicians, Arizona Medical Association, International Skeletal Society, Radiological Society of North America, American College of Radiology, American Medical Association, Society for Pediatric Radiology, Society of Nuclear Medicine and Molecular Imaging

Disclosure: Nothing to disclose.

Bernard D Coombs, MB, ChB, PhD Consulting Staff, Department of Specialist Rehabilitation Services, Hutt Valley District Health Board, New Zealand

Disclosure: Nothing to disclose.

David A Stringer, MBBS, FRCR, FRCPC Professor, National University of Singapore; Head, Diagnostic Imaging, KK Women’s and Children’s Hospital, Singapore

David A Stringer, MBBS, FRCR, FRCPC is a member of the following medical societies: Royal College of Physicians and Surgeons of Canada, Royal College of Radiologists, Society for Pediatric Radiology, British Columbia Medical Association, European Society of Paediatric Radiology

Disclosure: Nothing to disclose.

John Karani, MBBS, FRCR Clinical Director of Radiology and Consultant Radiologist, Department of Radiology, King’s College Hospital, UK

John Karani, MBBS, FRCR is a member of the following medical societies: British Institute of Radiology, Radiological Society of North America, Royal College of Radiologists, Cardiovascular and Interventional Radiological Society of Europe, European Society of Radiology, European Society of Gastrointestinal and Abdominal Radiology, British Society of Interventional Radiology

Disclosure: Nothing to disclose.

Lori Lee Barr, MD, FACR, FAIUM Clinical Assistant Professor of Radiology, University of Texas Medical Branch at Galveston School of Medicine; Member, Board of Directors, Austin Radiological Association; Consulting Staff, Seton Health Network, Columbia/St David’s Healthcare System, Healthsouth Rehabilitation Hospital of Austin, Georgetown Hospital, St Mark’s Medical Center, Cedar Park Regional Medical Center

Lori Lee Barr, MD, FACR, FAIUM is a member of the following medical societies: American Roentgen Ray Society, Association of University Radiologists, Southern Medical Association, Undersea and Hyperbaric Medical Society, American Society of Pediatric Neuroradiology, Society of Radiologists in Ultrasound, Texas Radiological Society, American Association for Women Radiologists, American College of Radiology, American Institute of Ultrasound in Medicine, Radiological Society of North America, Society for Pediatric Radiology

Disclosure: Nothing to disclose.

Imaging in Duodenal Atresia

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