International Clinical and Medical Case Reports Journal (ISSN: 2832-5788) | Volume 5, Issue 6 | Case Report | Open Access
Rajesh Puri*
Medanta, The Medicity, Gurugram India
*Correspondence to: Rajesh Puri
Fulltext PDFCronkhite-Canada syndrome (CCS) is a rare, non-inherited gastrointestinal polyposis syndrome characterized by diffuse hamartomatous polyps and ectodermal changes. We report a case of a 51-year-old woman presenting with chronic diarrhea, loss of taste, nail dystrophy, and alopecia, subsequently diagnosed with CCS. Early recognition and immunosuppressive therapy led to clinical and biochemical improvement.
Hiteshbhai Panchal, Raghavender Puri, Shubham, Harsh, Pawan Rawal, Lipika Lipi, et al. Cronkhite-Canada Syndrome Presenting as Chronic Diarrhea with Ectodermal Changes: A Case Report. Int Clinc Med Case Rep Jour. 2026;5(6):1-6.