منابع مشابه
Adult coeliac disease.
Only half the patients presented primarily with abdominal symptoms. Diarrhoea dominated the picture in thirty-three and pain was the main complaint in eleven. Most of the rest presented with the symptoms and signs of deficiency, chiefly of iron and folic acid, but also of calcium and the fat-soluble vitamins D and K, and albumin, a bad prognostic sign. When macrocytes and Howell Jolly bodies ar...
متن کاملAdult Coeliac Disease.
A clinical, biochemical, and pathological study is recorded of 50 patients in whom a diagnosis of idiopathic steatorrhea had been made and who had ;flat' jejunal biopsies. It is suggested that there is an underlying constitutional defect, not yet clearly defined, and that possibly secondary intestinal infection allows the intestinal mucosa to become sensitized to substances in the diet. Of thes...
متن کاملMalignancy and adult coeliac disease.
The suggestion has been made that malignancy anywhere in the body may be accompanied by intestinal mucosal changes similar to those found in adult coeliac disease (Creamer, 1964). The following case report indicates that characteristic jejunal mucosal changes, once reverted to normal by a gluten-free diet, do not reappear if a malignancy develops, providing that the gluten-free diet is maintained.
متن کاملCoeliac disease: clinical features in adult populations.
INTRODUCTION coeliac disease (CD) is a chronic disease of the small intestine, which is caused by gluten intolerance, producing malabsorption of nutrients and vitamins. Clinical manifestations of CD in adults are highly variable, including intestinal and extra-intestinal symptoms. The disease may also occur in individuals who are asymptomatic. OBJECTIVE our objective is to describe the incide...
متن کامل(HL-A) antigens in adult coeliac disease
In a study of histocompatibility antigens in adult coeliac disease the HL-A phenotypes have been determined in 117 patients and 149 of their first-degree relatives, of whom 94 had had a jejunal biopsy performed. There was an increased frequency ofthe HL-A 8 antigen in the patients and their relatives. Family studies showed no irregularity in the inheritance of both this antigen and the HL-A 1 a...
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ژورنال
عنوان ژورنال: Journal of Clinical Pathology
سال: 1974
ISSN: 0021-9746
DOI: 10.1136/jcp.27.9.710