Abstract

Coeliac disease (non-tropical sprue, gluten-sensitive enteropathy) is a chronic digestive insufficiency due to gluten-intolerance. Gluten or gliadin can be found in cereal products. There is a genetical predisposition and the disease tends to run in families. Atrophy of the villi in the small intestine is typical and leads to malabsorption and maldigestion. About one in 1000 people are affected, and more often women than men. Characteristic signs and symptoms include diarrhoea, flatulence, weight loss, and iron deficiency anaemia. However, cases with only few symptoms and the clinical picture of irritable colon or isolated lipase increase are not uncommon. Coeliac disease can be diagnosed by a biopsy of the mucosa of the duodenum and by detecting anti-transglutaminase antibodies. The only effective treatment is a strictly gluten-free diet. Immunosuppressive treatment is only rarely necessary. T-cell lymphoma of the small intestine is a long-term complication of insufficiently treated coeliac disease.

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