Cronkhite-Canada Syndrome: An Elusive Gastrointestinal Disorder With Multisystem Involvement - Pathogenesis, Diagnosis, And Therapeutic Strategies

    Araj Naveed Siddiqui, Rabia Hafsa, Vikash Kumar Karmani, Zainab Rehan, Rishi Chowdhary
    TLDR Cronkhite-Canada syndrome is a rare disorder needing early recognition and treatment with immunosuppressive therapies and nutritional support to manage symptoms and prevent complications.
    Cronkhite-Canada syndrome is a rare, non-hereditary gastrointestinal polyposis disorder characterized by multisystem involvement and significant diagnostic challenges due to its overlap with more common gastrointestinal diseases. This review synthesizes current evidence on its multifactorial pathogenesis, including immune dysregulation, microbiome alterations, and potential infectious triggers. It highlights the evolving role of immunosuppressive and biologic therapies, alongside nutritional support, in managing the condition. The article proposes a structured framework to improve early recognition, guide management, and reduce long-term complications, such as malignancy.
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