OBJECTIVE: Adult celiac disease is a genetically determined condition resul
ting from intolerance to gluten. This familial disease is associated with H
LA B8 DR3 and is characterized by cytotoxic T-lymphocyte reaction in the di
gestive wall leading to a maladsorption syndrome. Adult celiac disease woul
d be an expression of a silent disease already present in childhood.
PATIENTS AND METHODS: We conducted a retrospective study in 19 patients. Di
agnosis was established in a department of internal medicine in adulthood.
We analyzed histological findings and the clinical history and course.
RESULTS: The age curve at diagnosis peaked at 22 years and 67 years. Female
sex predominated. Average delay to diagnosis was 3.1 years. The patients w
ere admitted for reasons other than digestive disorders in 17 out of 1.9 ca
ses. Careful history taking did however disclose subtle digestive signs. Th
e principal manifestations wee hematological disorders such as chronic anem
ia, abnormal liver function tests, and poor control of associated diseases.
Type 1 diabetes mellitus was the main associated disease (4/19). Patients
with prolonged nutritional deficiencies experienced serious situations.
CONCLUSION: Adult celiac disease is a clinical Variant suggesting the prese
nce of other non-digestive disorders. Specific antibodies should be assayed
in patients with even minimal signs of deficiency in order to identify ass
ociated diseases. The principal cause of mortality is digestive T-cell lymp
homa. A gluten-free diet is essential to control the course of this chronic
disease.