| Literature DB >> 17198639 |
Eva Marín Serrano1, Pablo Guillén Mariscal, José Pérez-Requena, Paloma Rendón Unceta.
Abstract
Cronkhite-Canada syndrome is an infrequent, nonadenomatous, acquired polyposis that is associated with ectodermic alterations. The etiopathogenesis and optimal therapeutic management are unknown. We present a case of Cronkhite-Canada syndrome in a 58-year-old man who, after combined treatment with corticosteroids, disodium cromoglycate, loratadine, ciprofloxacin, and zinc, showed complete clinical and partial endoscopic remission. The polypoid lesions of Cronkhite-Canada syndrome can be reversed with medical treatment. Consequently, the natural history of the disease can be modified and its prognosis improved.Entities:
Mesh:
Year: 2006 PMID: 17198639 DOI: 10.1157/13095196
Source DB: PubMed Journal: Gastroenterol Hepatol ISSN: 0210-5705 Impact factor: 2.102