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Phenotype Characteristics of Patients with Colonic Serrated Polyposis Syndrome: a Study of 23 Cases

Overview
Journal Cir Esp
Specialty General Surgery
Date 2014 May 6
PMID 24795265
Citations 1
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Abstract

Introduction: Serrated polyposis syndrome (SPS) is a rare entity characterized by the presence of multiple hyperplastic polyps in the colon and an increased risk of presentation and development of colorectal cancer (CRC).

Objective: To evaluate the clinical and phenotypical characteristics of patients that present one of the 3 WHO criteria for the diagnosis of SPS diagnosed and treated a tour hospital.

Patients And Methods: Patients with the diagnosis of SPS during 2005-2012 were revised; 24.208 colonoscopies were performed during this period. Age, sex, family history of CRC (APC/MYH), proximal/mixed/distal phenotype, indication for colonoscopy, number, size, location of the hyperplastic polyps, presence of mixed/adenomatous polyps, CRCI, follow-up and endoscopio/surgical treatment.

Results: A total of 23 cases were included (19 male). The median age was 51. A total of 34% had a prior family history of CRC or polpyps. Distal phenotype was more frequent (48%). Another 73% presented synchronous adenomatous polyps, and 26% a CRC. A total of 57% were asymptomatic. Surgery was performed in 9 cases (6 for cancer and 3 for polyposis), and 14 were treated by polypectomy and observation. Eleven patients (47%) presented recurrent/persistent lesions after initial surgical/endoscopic treatment.

Conclusion: SPS is an heterogeneous syndrome that is variable in the type, size, distribution and number of polyps, and is more common in male smokers with a distal phenotype. The majority of patients also present synchronous adenomatous polyps. These patients require an organized multidisciplinary evaluation.

Citing Articles

Clinical characteristics of patients with serrated polyposis syndrome in Korea: comparison with Western patients.

Ran Kim E, Jeon J, Lee J, Lee Y, Hong S, Kyung Chang D Intest Res. 2017; 15(3):402-410.

PMID: 28670238 PMC: 5478766. DOI: 10.5217/ir.2017.15.3.402.