| Literature DB >> 25954656 |
Abstract
Cronkhite-Canada syndrome (CCS) is an extremely rare non-inherited condition characterized by gastrointestinal hamartomatous polyposis, alopecia, onychodystrophy, hyperpigmentation, weight loss and diarrhoea. The aetiology is probably autoimmune and diagnosis is based on history, physical examination, endoscopic findings of gastrointestinal polyposis, and histology. The disease is very rare; approximately 450 cases of CCS have been reported worldwide. The author reports a case of CCS in an elderly Indian male.Entities:
Keywords: Alopecia; Hyperpigmentation; Onychodystrophy; Polyposis
Year: 2015 PMID: 25954656 PMCID: PMC4413105 DOI: 10.7860/JCDR/2015/11919.5700
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X