syndrome

pylori gastritis and juvenile colonic polyposis and was thought to have Cronkhite-Canada syndrome (CCS) but was not confirmed in genetic assessment.

Mazaki et al., "Spontaneous regression of polyposis following abdominal colectomy and Helicobacter pylori eradication for Cronkhite-Canada syndrome," Case Reports in Gastroenterology, vol.

Alopecia, "Cronkhite-Canada syndrome (CCS)--a rare case report," Journal of Clinical and Diagnostic Research, vol.

The gastric polyps were also a characteristic of Cronkhite-Canada syndrome. The foveolar glands were elongated, irregular, and focally dilated.

Based on these clinical, endoscopic, and histopathologic features, a diagnosis of Cronkhite-Canada Syndrome was made.

Boardman, "Cronkhite-Canada syndrome hamartomatous polyps are infiltrated with IgG4 plasma cells," Digestion, vol.

Thus, a diagnosis of Cronkhite-Canada syndrome was made, considering the characteristic ectodermal abnormalities on physical examination, endoscopic findings and histology.

First described in 1955, Cronkhite-Canada syndrome (CCS) is a rare, nonhereditary polyposis syndrome with an uncertain aetiopathogenesis.

Chakrabarti, "Cronkhite-Canada Syndrome (CCS)--a rare case report," Journal of Clinical and Diagnostic Research, vol.

Lunn, "Cronkhite-Canada syndrome: an unusual finding of gastro-intestinal adenomatous polyps in a syndrome characterized by hamartomatous polyps," Gastroenterology Report, vol.

Cronkhite-Canada syndrome is a sporadic disease with multiple polyps in the gastrointestinal tract.

Hyser, "A case of Cronkhite-Canada syndrome and a review of gastrointestinal polyposis syndromes," Gastroenterology and Hepatology, vol.

[29] reported a 63-yearold lady with Cronkhite-Canada syndrome who developed colorectal cancer.

Metz, "A case of Cronkhite-Canada syndrome with taste disturbance as a leading complaint," Digestion, vol.