Published online Dec 28, 2022. doi: 10.3748/wjg.v28.i48.6950
Peer-review started: October 2, 2022
First decision: November 3, 2022
Revised: November 14, 2022
Accepted: December 13, 2022
Article in press: December 13, 2022
Published online: December 28, 2022
Processing time: 85 Days and 22.5 Hours
Colonic polyposis syndromes typically result from germline mutations in the APC or MUTYH genes and less commonly from other low/intermediate-risk genes. When no pathogenic variant is identified, a diagnosis of colonic polyposis of unknown etiology (CPUE) is made.
The existing literature on CPUE is limited, and the precise clinical features and long-term outcomes are not well-defined.
To characterize the natural history of CPUE by defining the malignancy risk, long-term colonic adenoma burden, and risk of extra-colonic tumors over an extended period of surveillance.
We performed a retrospective detailed chart review of demographic, lifestyle habits, endoscopic, genetic, and clinical data of patients aged 18 years old or older meeting the criteria for CPUE in the Hereditary Gastrointestinal Cancer Database at Massachusetts General Hospital.
70 patients met the inclusion criteria and were predominantly Caucasian males. During an extended surveillance period, a very low cumulative colonic adenoma burden was observed, with no evidence for duodenal adenomas. 4 patients were diagnosed with colorectal cancer (CRC), but none had extra-colonic malignancies that are typically seen in familial adenomatous polyposis (FAP) syndrome (i.e., gastric, duodenal, or thyroid cancer). There was no mortality attributable to CRC.
Individuals with CPUE exhibited a relatively mild course with respect to polyp burden and cancer risk, which differs significantly from the FAP syndrome. The modest colonic burden implies colonoscopy surveillance intervals could be extended, and regular gastroscopic exams may not be necessary.
CPUE is an underdiagnosed and heterogeneous clinical entity. The current findings should be validated in large-scale multi-center prospective studies, with greater representation of non-Caucasian populations in order to better define this unique condition in an evidence-based approach.