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Cronkhite-Canada syndrome: treatment responses and improved overall survival.
Pham JT, Kisiel JB, Sweetser S. Pham JT, et al. Int J Colorectal Dis. 2023 Feb 13;38(1):39. doi: 10.1007/s00384-023-04332-w. Int J Colorectal Dis. 2023. PMID: 36781513
BACKGROUND: Cronkhite-Canada syndrome (CCS) is considered a relentlessly progressive disease with high mortality rates. ...All patients received an initial prednisone dose equivalence of 30-80 mg daily, and five patients required steroids at the time of the l …
BACKGROUND: Cronkhite-Canada syndrome (CCS) is considered a relentlessly progressive disease with high mortality rates. …
Pharmacological management of Cronkhite-Canada syndrome.
Ward EM, Wolfsen HC. Ward EM, et al. Expert Opin Pharmacother. 2003 Mar;4(3):385-9. doi: 10.1517/14656566.4.3.385. Expert Opin Pharmacother. 2003. PMID: 12614190 Review.
Cronkhite-Canada syndrome (CCS) is a rare, non-inherited gastrointestinal polyposis syndrome associated with characteristic ectodermal abnormalities. A number of potentially life-threatening complications including malnutrition, gastrointestinal bleedi …
Cronkhite-Canada syndrome (CCS) is a rare, non-inherited gastrointestinal polyposis syndrome associated with cha …
Endoscopic and clinical evaluation of treatment and prognosis of Cronkhite-Canada syndrome: a Japanese nationwide survey.
Watanabe C, Komoto S, Tomita K, Hokari R, Tanaka M, Hirata I, Hibi T, Kaunitz JD, Miura S. Watanabe C, et al. J Gastroenterol. 2016 Apr;51(4):327-36. doi: 10.1007/s00535-015-1107-7. Epub 2015 Jul 28. J Gastroenterol. 2016. PMID: 26216651 Free PMC article.
BACKGROUND: First reported in 1955, Cronkhite-Canada syndrome (CCS), a rare syndrome characterized by ectodermal abnormalities and inflammatory changes of the gastrointestinal tract mucosa, has been associated with a poor prognosis and life-threatening …
BACKGROUND: First reported in 1955, Cronkhite-Canada syndrome (CCS), a rare syndrome characterized by ectodermal …
Clinicopathologic features and treatment outcomes in Cronkhite-Canada syndrome: support for autoimmunity.
Sweetser S, Ahlquist DA, Osborn NK, Sanderson SO, Smyrk TC, Chari ST, Boardman LA. Sweetser S, et al. Dig Dis Sci. 2012 Feb;57(2):496-502. doi: 10.1007/s10620-011-1874-9. Epub 2011 Sep 1. Dig Dis Sci. 2012. PMID: 21881972
BACKGROUND AND AIMS: Cronkhite-Canada syndrome (CCS) is a noninherited condition, associated with high morbidity, and characterized by gastrointestinal hamartomatous polyposis, alopecia, onychodystrophy, hyperpigmentation, and diarrhea. All features may respo …
BACKGROUND AND AIMS: Cronkhite-Canada syndrome (CCS) is a noninherited condition, associated with high morbidity, and c …
The challenging diagnosis of Cronkhite-Canada syndrome in the upper gastrointestinal tract: a series of 7 cases with clinical follow-up.
Bettington M, Brown IS, Kumarasinghe MP, de Boer B, Bettington A, Rosty C. Bettington M, et al. Am J Surg Pathol. 2014 Feb;38(2):215-23. doi: 10.1097/PAS.0000000000000098. Am J Surg Pathol. 2014. PMID: 24418855
Cronkhite-Canada syndrome is a rare protein-losing enteropathy, classically characterized by ectodermal changes and gastrointestinal polyposis. ...In only 1 patient, a significant increase in IgG4-positive plasma cells was observed in a colonic polyp. In summ …
Cronkhite-Canada syndrome is a rare protein-losing enteropathy, classically characterized by ectodermal changes and gas …