©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 28, 2024; 30(8): 984-990
Published online Feb 28, 2024. doi: 10.3748/wjg.v30.i8.984
Published online Feb 28, 2024. doi: 10.3748/wjg.v30.i8.984
Cronkhite-Canada syndrome with esophagus involvement and six-year follow-up: A case report
Yu-Chen Tang, Department of Endocrinology, The First Affiliated Hospital of Ningbo University, Ningbo 315000, Zhejiang Province, China
Author contributions: Tang YC contributed to data collection, case analysis and manuscript writing.
Supported by the Medical Health Science and Technology Project of Zhejiang Province , No. 2022KY1109 ; the Natural Science Foundation of Ningbo , No. 2022J204 ; and Ningbo Key Clinical Specialty (Endocrinology) , No. 2022-B07 .
Informed consent statement: Informed written consent was obtained from the patient for publication of this report and any accompanying images.
Conflict-of-interest statement: The author declare that they have no conflict of interest to disclose.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Corresponding author: Yu-Chen Tang, MD, Attending Doctor, Department of Endocrinology, The First Affiliated Hospital of Ningbo University, No. 59 Liuting Street, Ningbo 315000, Zhejiang Province, China. fyytangyuchen@nbu.edu.cn
Received: September 28, 2023
Peer-review started: September 28, 2023
First decision: December 28, 2023
Revised: January 5, 2024
Accepted: January 25, 2024
Article in press: January 25, 2024
Published online: February 28, 2024
Processing time: 150 Days and 21.8 Hours
Peer-review started: September 28, 2023
First decision: December 28, 2023
Revised: January 5, 2024
Accepted: January 25, 2024
Article in press: January 25, 2024
Published online: February 28, 2024
Processing time: 150 Days and 21.8 Hours
Core Tip
Core Tip: Cronkhite-Canada syndrome is a rare, noninherited disease characterized by gastrointestinal polyposis with diarrhea and ectodermal abnormalities. We report a case of a 63-year-old man with numerous polyps scattered throughout the digestive tract, including the esophagus. Comprehensive corticosteroid treatment can result in partial or full remission of clinical symptoms.