Bulb biopsies for the diagnosis of celiac disease in pediatric patients

Gastrointest Endosc. 2010 Sep;72(3):564-8. doi: 10.1016/j.gie.2010.05.021. Epub 2010 Jul 13.

Abstract

Background: Celiac disease (CD) is a gluten-dependent enteropathy. The current standard for diagnosing CD involves obtaining 4 biopsy samples from the descending duodenum. It has been suggested that duodenal bulb biopsies may also be useful.

Objective: To assess the utility of bulbar biopsies for the diagnosis of CD in pediatric patients.

Design: Prospective study.

Setting: Single center.

Patients: Forty-seven consecutively enrolled pediatric patients with celiac serologies and a clinical suspicion of CD.

Interventions: All patients underwent EGD, and 4 biopsy samples were obtained from the duodenal bulb and 4 from the descending duodenum of each child.

Main outcome measurements: The pathologist blindly reported the Marsh histological grade for the diagnosis of CD of the bulb and descending duodenum.

Results: The diagnosis of CD was histologically confirmed in 89.4% (42/47) of the cases of biopsy samples obtained from the descending duodenum and in all 47 obtained from the bulb. In 35 patients (74.5%), histology was the same in the bulb and duodenum; in 11 (23.4%) cases, the grade of atrophy was higher in the bulb than in the descending duodenum, and 5 (10.6%) had bulb histology positive for CD but negative duodenal findings. One child (2.1%) had a higher histological grade in the duodenum than in the bulb. The diagnostic gain with bulbar biopsies was 10.6%.

Limitations: Small sample and absence of a comparison group (asymptomatic children with normal CD antibodies).

Conclusions: We suggest examining 4 biopsy samples from the duodenal bulb and 4 from the descending duodenum to improve diagnostic accuracy of CD.

Publication types

  • Comparative Study

MeSH terms

  • Atrophy
  • Biopsy / methods
  • Celiac Disease / pathology*
  • Child
  • Duodenoscopy / methods*
  • Duodenum / pathology*
  • Female
  • Humans
  • Intestinal Mucosa / pathology
  • Lymphocytes / pathology
  • Male
  • Predictive Value of Tests
  • Prospective Studies