SSLs are thought to lead to colorectal cancer through the (alternate) serrated pathway.[1][2] This differs from most colorectal cancer, which arises from mutations starting with inactivation of the APC gene.
The serrated polyposis syndrome (SPS) is a relatively rare condition characterized by multiple and/or large serrated polyps of the colon. Serrated polyps include SSLs, hyperplastic polyps, and traditional serrated adenomas. Diagnosis of this disease is made by the fulfillment of any of the World Health Organization's (WHO) clinical criteria.[4]
Diagnosis
SSLs are diagnosed by their microscopic appearance; histomorphologically, they are characterized by (1) basal dilation of the crypts, (2) basal crypt serration, (3) crypts that run horizontal to the basement membrane (horizontal crypts), and (4) crypt branching. The most common of these features is basal dilation of the crypts.[citation needed]
High magnification micrograph of a SSL showing crypt branching.
Treatment
Complete removal of a SSL is considered curative.
Several SSLs confer a higher risk of subsequently finding colorectal cancer and warrant more frequent surveillance. The surveillance guidelines are the same as for other colonicadenomas. The surveillance interval is dependent on (1) the number of adenomas, (2) the size of the adenomas, and (3) the presence of high-grade microscopic features.[5]
Epidemiology
Sessile serrated lesions account for about 25% of all serrated polyps.[6] Advanced SSLs with cytological dysplasia are rare in younger patients,[7] and progression of SSLs appears to be linked with ageing.[8][9]
History
Sessile serrated adenomas were first described in 1996.[10] In 2019, the World Health Organization recommended the use of the term "sessile serrated lesion," rather than sessile serrated polyp or adenoma.[6]
^World J Gastroenterol 2012 May 28; 18(20): 2452–2461
^Levine JS, Ahnen DJ (December 2006). "Clinical practice. Adenomatous polyps of the colon". N. Engl. J. Med. 355 (24): 2551–7. doi:10.1056/NEJMcp063038. PMID17167138.
^Bettington, M; Brown, I; Rosty, C; Walker, N; Liu, C; Croese, J; Rahman, T; Pearson, SA; McKeone, D; Leggett, B; Whitehall, V (March 2019). "Sessile Serrated Adenomas in Young Patients may have Limited Risk of Malignant Progression". Journal of Clinical Gastroenterology. 53 (3): e113 –e116. doi:10.1097/MCG.0000000000001014. PMID29570172. S2CID4261352.
^Torlakovic, E; Snover, DC (July 2006). "Sessile serrated adenoma: a brief history and current status". Critical Reviews in Oncogenesis. 12 (1–2): 27–39. doi:10.1615/critrevoncog.v12.i1-2.30. PMID17078205.