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Gastroenterology and Hepatology from Bed to Bench. 2016; 9 (1): 58-63
de Anglais | IMEMR | ID: emr-174984

RÉSUMÉ

Cronkhite- Canada syndrome [CCS] considered as a rare and non-hereditary disorder. Gastrointestinal polyposis and diarrhea along with some extra signs and symptoms such as hypoproteinemia, and epidermal manifestations are recognized in this syndrome. The pathophysiology of this syndrome is not completely understood and it seems that inflammatory processes may be involved. We present a 50 year-old man with hamartomatous polyps throughout the colon and long-lasting diarrhea not responding to typical therapies during three years


Sujet(s)
Mâle , Adulte d'âge moyen , Humains , Littérature de revue comme sujet , Syndromes néoplasiques héréditaires , Syndrome de Peutz-Jeghers
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