collagenous gastritis is a rare histopathological disorder of unknown
origin, characterized by a subepithelial collagen deposit greater than
10 mu m thick, associated with an inflammatory infiltrate of the gast
ric mucosa. This report describes a second pediatric case of collageno
us gastritis, revealed by severe anemia caused by gastric bleeding, as
was the first case. Unlike the adult cases of collagenous gastritis,
lesions were limited to the stomach, and remained unchanged on six ser
ies of biopsies taken during a 30 month follow-up, despite treatment w
ith omeprazole, sucralfate and corticosteroids. An immunohistochemical
study showed signs of local immune activation on all biopsy specimens
, including overexpression of HLA-DR by epithelial cells, increased nu
mbers of CD3+ intraepithelial lymphocytes, and CD25+ cells in the lami
na propria. Although the cause of the disease remains unclear, our fin
dings suggest that the histopathological lesions of collagenous gastri
tis may result from a local immune process. Copyright (C) 1998 by W.B.
Saunders Company.