•Mô hình khảm của niêm mạc tá tràng ở trẻ có celiac không được điều trị

•Sinh thiết ít nhất 6 mẫu để chẩn đoán bệnh

•Chế độ ăn không gluten như bột mì

Celiac sprue

Partial and total villous atrophy may be the endpoint of different pathological processes, including celiac sprue, giardiasis, cow’s milk allergy, postinfectious inflammation, and immunodeficiency. Clinical manifestations of these diseases are non-specific.

For more than three decades jejunal capsule biopsy was the cornerstone for diagnosis of celiac sprue. But it is time-consuming, requires fluoroscopy, and is associated with failure of adequate tissue sampling. It has been replaced by endoscopic biopsies in adults and children. Endoscopic assessment of the duodenal mucosa in conjunction with chromoendoscopy and waterimmerging technique targets the biopsy minimizing the false negative results in patients with patchy distribution of villous atrophy. In addition, accidental discovery of mucosal changes suggestive of celiac sprue during EGD in children is not uncommon. The main endoscopic sign of celiac sprue in children is a mosaic pattern of the duodenal and jejunal mucosa and “scalloping” of the valvulae conniventes.

In the active phase of celiac disease, the duodenal mucosa appears grayish, edematous and a mosaic with an increased vascular pattern in the proximal duodenum. Duodenal folds are coarse and have scalloped appearance. Mucosa between the duodenal folds has a mosaic or honeycomb pattern. These endoscopic signs are usually more prominent in the distal duodenum or proximal jejunum. Although duodenal or jejunal mucosa are not friable, biopsy is associated with slightly more intensive bleeding.

The final diagnosis of celiac sprue is histological. At least four biopsies from the distal portion of duodenum are required. All specimens have to be properly oriented for correct assessment of the villous and cryptal pattern.

Complete regeneration of atrophic mucosa is expected within 6 months in children on a strict gluten-free diet. In noncompliant children, espe- cially adolescents, mucosal atrophy may be clinically silent