[Sonography of small bowel, colon and appendix in children with cystic fibrosis]

Maria Uliasz1, Hanna Bragoszewska, Beata Iwanowska

  • 1Zaklad Diagnostyki Obrazowej IMiD. mariauliasz@wp.pl

Medycyna Wieku Rozwojowego
|July 9, 2010
PubMed

Insights

Sonography effectively detects frequent intestinal changes in children with cystic fibrosis (CF). This imaging is crucial for annual CF follow-up and aids in diagnosing unidentified CF cases.

Area of Science:

  • Pediatric gastroenterology
  • Medical imaging
  • Genetics and hereditary diseases

Background:

  • Cystic fibrosis (CF) is a genetic disorder affecting multiple organs, particularly the gastrointestinal tract.
  • Early and accurate diagnosis of CF-related complications is essential for effective management.
  • Sonography offers a non-invasive method for evaluating abdominal pathology.

Purpose of the Study:

  • To evaluate the diagnostic utility of sonography in identifying and characterizing intestinal and abdominal organ abnormalities in pediatric patients with cystic fibrosis.
  • To determine the incidence of pathological changes in the intestines and other abdominal organs in children with CF.
  • To assess the role of abdominal sonography in the diagnosis of unidentified CF cases.

Main Methods:

  • A cohort of 182 children (2 months to 22 years) with diagnosed or suspected cystic fibrosis underwent sonographic examinations.
  • A control group of 20 children was included for comparison.
  • Philips ultrasound equipment with various probes was utilized over a 2.5-year period, with multiple examinations performed on some patients.

Main Results:

  • Intestinal changes were observed in 59.3% of children with CF, including colon (53.3%) and small intestine (26.9%) abnormalities.
  • Significantly increased intestinal wall thickness was noted in CF patients compared to controls.
  • Abnormalities in the liver (39%) and pancreas (62.6%) were frequently identified, alongside enlarged mesenteric lymph nodes (46%).

Conclusions:

  • Sonography reveals a high prevalence of intestinal and abdominal organ changes in children with cystic fibrosis.
  • Routine annual sonographic examination should be incorporated into the follow-up care of pediatric CF patients.
  • Abdominal sonography is a valuable tool for diagnosing cystic fibrosis when the condition is not initially identified.
Abstract

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