Ko Huaibin M, Harpaz Noam, McBride Russell B, Cui Miao, Ye Fei, Zhang David, Ullman Thomas A, Polydorides Alexandros D
Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Medicine (Gastroenterology), Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Mod Pathol. 2015 Dec;28(12):1584-93. doi: 10.1038/modpathol.2015.111. Epub 2015 Sep 25.
Serrated colorectal polyps, which, besides hyperplastic polyps, comprise sessile serrated adenomas/polyps and traditional serrated adenomas, are presumptive precursors of at least 20% of sporadic colorectal carcinomas; however, their significance in patients with inflammatory bowel disease is unclear. We retrospectively evaluated 78 serrated polyps, removed over a 14-year period from 6602 inflammatory bowel disease patients undergoing endoscopic surveillance, with respect to morphologic, clinicopathologic, and molecular features, and compared rates of advanced neoplasia (high-grade dysplasia and carcinoma) development following the index serrated polyp diagnosis to reference inflammatory bowel disease cohorts without serrated polyps. Serrated polyps negative for dysplasia, which morphologically resembled sporadic sessile serrated adenoma/polyps, occurred mainly in females, in the proximal colon, and contained BRAF mutations. Serrated polyps with low-grade dysplasia resembled sporadic traditional serrated adenomas and occurred mainly in males, in the distal colon, and contained KRAS mutations. Serrated polyps indefinite for dysplasia were morphologically heterogeneous, but similar to serrated polyps positive for low-grade dysplasia with respect to male predominance, left-sided location, and KRAS mutation rates. Rates of prevalent neoplasia associated with serrated polyps positive for low-grade dysplasia, indefinite for dysplasia, and negative for dysplasia were 76, 39, and 11%, respectively (P<0.001). Actuarial 10-year rates of incident advanced neoplasia after an initial diagnosis of serrated polyp positive for low-grade dysplasia, indefinite for dysplasia, and negative for dysplasia were 17, 8, and 0%, respectively, the first and last being significantly different (P=0.02) and comparable to those of corresponding reference populations of inflammatory bowel disease patients with and without low-grade dysplasia at baseline, respectively. We conclude that in serrated polyps from inflammatory bowel disease patients, dysplasia grade correlates with morphology, sex, anatomic location, BRAF and KRAS mutation status, prevalent conventional neoplasia, and rates of advanced neoplasia development.
锯齿状结直肠息肉,除增生性息肉外,还包括无蒂锯齿状腺瘤/息肉和传统锯齿状腺瘤,是至少20%的散发性结直肠癌的推定前体;然而,它们在炎症性肠病患者中的意义尚不清楚。我们回顾性评估了在14年期间从6602例接受内镜监测的炎症性肠病患者中切除的78个锯齿状息肉,分析其形态学、临床病理和分子特征,并将首次诊断为锯齿状息肉后高级别瘤变(高级别异型增生和癌)的发生率与无锯齿状息肉的炎症性肠病参考队列进行比较。异型增生阴性的锯齿状息肉,形态上类似于散发性无蒂锯齿状腺瘤/息肉,主要发生在女性、近端结肠,且含有BRAF突变。低级别异型增生的锯齿状息肉类似于散发性传统锯齿状腺瘤,主要发生在男性、远端结肠,且含有KRAS突变。异型增生不确定的锯齿状息肉在形态上具有异质性,但在男性优势、左侧位置和KRAS突变率方面与低级别异型增生阳性的锯齿状息肉相似。低级别异型增生阳性、异型增生不确定和异型增生阴性的锯齿状息肉相关的瘤变患病率分别为76%、39%和11%(P<0.001)。初次诊断为低级别异型增生阳性、异型增生不确定和异型增生阴性的锯齿状息肉后,10年累积新发高级别瘤变率分别为17%、8%和0%,第一个和最后一个有显著差异(P=0.02),分别与基线时有无低级别异型增生的炎症性肠病患者相应参考人群的发生率相当。我们得出结论,在炎症性肠病患者的锯齿状息肉中,异型增生分级与形态、性别、解剖位置、BRAF和KRAS突变状态、常见的传统瘤变以及高级别瘤变发生率相关。