Citation, DOI & article data
There is a recognized male predilection (M:F 3:2). Patients typically are middle-aged (50-60 years of age) 1. 75% of the ~500 cases in the literature are from Japan 7.
Patients typically present with watery diarrhea and a protein-losing enteropathy with associated nail atrophy, brownish skin pigmentation, and alopecia 3.
Cronkhite-Canada syndrome is characterized by numerous hamartomatous polyps in the digestive tract, with predominant involvement of the stomach, large intestine and, to a lesser extent, small bowel. The exact etiology is unknown and there is no recognized familial occurrence. Unlike other polyposis syndromes, it is not associated with malignancy.
Polyps are similar to those of juvenile polyposis syndrome except that the mucosa among Cronkhite-Canada syndrome polyps is edematous and inflammation of the lamina propria is usually present; by contrast, histologically the mucosa between juvenile polyposis syndrome polyps is normal 4.
On barium studies, this syndrome is characterized by polyposis involving the entire gastrointestinal tract. Gastric and colonic polyposis are both present in 100% of patients with this diagnosis. Small bowel involvement is seen in 50% of patients.
History and etymology
This syndrome was initially described by American physician Leonard W Cronkhite Jr (1919-1996) 6 and American radiology fellow Wilma Jeanne Canada (1926-2017) 5 in 1955, both working at Massachusetts General Hospital 2.
Dr Canada became Dr Canada Diner after she married and spent her whole post-fellowship career at the University of Arkansas for Medical Sciences in Little Rock, Arkansas, retiring as Professor of Radiology in 1997 5.
- 1. Harned RK, Buck JL, Sobin LH. The hamartomatous polyposis syndromes: clinical and radiologic features. AJR Am J Roentgenol. 1995;164 (3): 565-71. AJR Am J Roentgenol (abstract) - Pubmed citation
- 2. Cronkhite LW, Canada WJ. Generalized gastrointestinal polyposis; an unusual syndrome of polyposis, pigmentation, alopecia and onychotrophia. N. Engl. J. Med. 1955;252 (24): 1011-5. Pubmed citation
- 3. Brant WE, Helms CA. Fundamentals of Diagnostic Radiology. Lippincott Williams & Wilkins. (2007) ISBN:0781761352. Read it at Google Books - Find it at Amazon
- 4. Burke AP, Sobin LH. The pathology of Cronkhite-Canada polyps. A comparison to juvenile polyposis. Am. J. Surg. Pathol. 1989;13 (11): 940-6. Pubmed citation
- 5. Teresita L. Angtuaco, Edgardo J. C. Angtuaco. Wilma C. Diner, MD. (2017) Radiology. 283 (1): 310. doi:10.1148/radiol.2017174002 - Pubmed
- 6. https://www.thecrimson.com/article/1996/7/23/former-chief-of-childrens-hospital-dead/
- 7. Schulte S, Kütting F, Mertens J, et al. Case report of patient with a Cronkhite-Canada syndrome: sustained remission after treatment with corticosteroids and mesalazine. (2019) BMC gastroenterology. 19 (1): 36. doi:10.1186/s12876-019-0944-x - Pubmed