Background. Endoscopic abnormalities have been described in adult patients
with celiac disease that may suggest the diagnosis, especially when the pre
sentation is atypical.
Methods: The duodenum of 140 children undergoing EGD for various different
indications was evaluated macroscopically and histologically.
Results: Histology revealed total villous atrophy in 80 patients, 79 of who
m had celiac disease. Among these, 100% had a mucosal mosaic pattern in the
duodenum (sensitivity 98.7%, specificity 96.7%, positive predictive value
97.5%, negative predictive value 98.3%), 70% had scalloped duodenal folds (
sensitivity 68.7%, specificity 98.3%, positive predictive value 98.2%, nega
tive predictive value 70.2%),15% had visible vasculature, and 6% had reduct
ion of duodenal folds. Sensitivity and specificity of endoscopic findings w
ere not modified by chromoendoscopy. Except for the mosaic pattern, the fre
quency of endoscopic abnormalities increased with age; reduction of duodena
l folds was never seen in children with celiac disease who were less than 5
years of age.
Conclusions: The frequency and diagnostic value of endoscopic abnormalities
are different in children with celiac disease compared with adults with th
is disease. Because indications for endoscopy, such as abdominal pain, dysp
epsia, and unexplained anemia, can be manifestations of celiac disease, and
villous atrophy may have a patchy distribution, awareness of these endosco
pic abnormalities is important in the diagnosis of celiac disease in childr
en.