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Serrated polyposis syndrome
Medical condition / From Wikipedia, the free encyclopedia
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Serrated polyposis syndrome (SPS), previously known as hyperplastic polyposis syndrome, is a disorder characterized by the appearance of serrated polyps in the colon. While serrated polyposis syndrome does not cause symptoms, the condition is associated with a higher risk of colorectal cancer (CRC). The lifelong risk of CRC is between 25 and 40%. SPS is the most common polyposis syndrome affecting the colon, but is under recognized due to a lack of systemic long term monitoring.[5] Diagnosis requires colonoscopy, and is defined by the presence of either of two criteria: five or more serrated lesions/polyps proximal to the rectum (all ≥ 5 mm in size, with two lesions ≥10 mm), or more than 20 serrated lesions/polyps of any size distributed throughout the colon with five proximal to the rectum.[6]
Serrated polyposis syndrome | |
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Other names | Hyperplastic polyposis syndrome (former) |
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Hyperplastic polyp seen under microscopy with H&E stain | |
Specialty | Gastroenterology |
Symptoms | Asymptomatic |
Complications | Colorectal cancer (~20%)[1] |
Usual onset | 55 years of age (average)[2] |
Types | Distal and proximal |
Causes | Environmental and genetic factors |
Risk factors | Smoking, Lymphoma[3] |
Diagnostic method | Colonoscopy |
Treatment | Surveillance colonoscopy Polypectomy Surgery |
Frequency | 0.03–0.5%.[4] |
A family history of SPS and smoking tobacco are associated with a higher risk of serrated polyposis syndrome, whereas the use of aspirin and nonsteroidal anti-inflammatory drugs (NSAIDs) are associated with a lower risk. While the only validated genetic cause of SPS is mutations in RNF43,[7] additional important genetic abnormalities include BRAF mutations, abnormal CpG island methylator phenotype, and microsatellite instability. However, most individuals with the syndrome do not have an associated germline mutation. The types of polyps found in SPS include sessile serrated adenomas/polyps, traditional serrated adenomas, and hyperplastic polyps. SPS occurs in two phenotypes: proximal and distal. Proximal SPS has a greater risk of CRC than distal SPS.
The vast majority of cases may be managed with colonoscopy with removal polyps (polypectomy). Polyp removal is recommended to decrease the risk of colorectal cancer. Repeat colonoscopy should be performed every one to three years. If polyps are very large, numerous, or increase in number rapidly, then surgery may be necessary. Surgery may also be warranted if CRC is suspected or confirmed. First-degree relatives of people with SPS have an increased risk of CRC, and should undergo early screening with colonoscopy.