Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA, 15213, USA.
Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, USA.
Hum Pathol. 2021 Jun;112:9-19. doi: 10.1016/j.humpath.2021.03.002. Epub 2021 Mar 13.
Serrated epithelial change (SEC) manifests in patients with long-standing inflammatory bowel disease (IBD) and is characterized by disorganized crypt architecture, irregular serrations, and goblet cell-rich epithelium. The serrated nature of SEC is reminiscent of serrated colorectal polyps, which frequently harbor KRAS/BRAF mutations. SEC is, however, not only histologically distinct from sporadic serrated polyps but also associated with colorectal neoplasia. Whether SEC is a precursor to IBD-associated neoplasia remains unclear. To further define the relationship of SEC with serrated colorectal polyps and IBD-associated neoplasia, we performed targeted next-generation sequencing on colorectal specimens to include the following: SEC without dysplasia/neoplasia (n = 10), SEC with separate foci of associated dysplasia/adenocarcinoma from the same patients (n = 17), and uninvolved mucosa (n = 10) from 14 patients. In addition, we molecularly profiled sessile serrated lesion (SSL)-like or serrated lesion, not otherwise specified (SL-NOS), specimens, from 11 patients who also had IBD. This control cohort included SSL-like/SL-NOS without dysplasia/neoplasia (n = 11), SSL-like/SL-NOS with associated low-grade dysplasia (n = 2), and uninvolved mucosa (n = 8). By next-generation sequencing, the most frequently mutated gene in SEC without neoplasia and associated dysplasia/adenocarcinoma from separate foci in the same patients was TP53. Recurrent TP53 mutations were present in 50% of SEC specimens without dysplasia/neoplasia. In addition, alterations in TP53 were detected at a prevalence of 71% in low-grade dysplasia, 83% in high-grade dysplasia, and 100% in adenocarcinoma. Paired sequencing of SEC and associated neoplasia revealed identical TP53 missense mutations for 3 patients. In contrast, 91% of SSL-like/SL-NOS specimens without dysplasia/neoplasia harbored KRAS/BRAF mutations, which were conserved in associated low-grade dysplasia. No genomic alterations were found in uninvolved mucosa from either patients with SEC or patients with SSL-like/SL-NOS. Based on our findings, we conclude SEC is distinct from SSL-like serrated colorectal lesions in patients with IBD and an early precursor to IBD-associated neoplasia that warrants colonoscopic surveillance.
锯齿状上皮改变(SEC)发生于长期患有炎症性肠病(IBD)的患者中,其特征为隐窝结构紊乱、锯齿状不规则和杯状细胞丰富的上皮。SEC 的锯齿状特征类似于锯齿状结直肠息肉,这些息肉常含有 KRAS/BRAF 突变。然而,SEC 不仅在组织学上与散发性锯齿状息肉不同,而且与结直肠肿瘤有关。SEC 是否是 IBD 相关肿瘤的前体尚不清楚。为了进一步明确 SEC 与锯齿状结直肠息肉和 IBD 相关肿瘤的关系,我们对结直肠标本进行了靶向下一代测序,包括以下内容:无发育不良/肿瘤的 SEC(n=10)、来自同一患者的与 SEC 分开的相关发育不良/腺癌病灶的 SEC(n=17)和 14 名患者的未受影响的粘膜(n=10)。此外,我们对 11 名患有 IBD 的患者的无蒂锯齿状病变(SSL)样或锯齿状病变,其他未特指(SL-NOS)标本进行了分子分析。该对照组包括无发育不良/肿瘤的 SSL 样/SL-NOS(n=11)、伴有低度发育不良的 SSL 样/SL-NOS(n=2)和未受影响的粘膜(n=8)。通过下一代测序,在无肿瘤和与 SEC 分开的病灶相关发育不良/腺癌的患者中,最常突变的基因是 TP53。无发育不良/肿瘤的 SEC 标本中 50%存在 TP53 反复突变。此外,在低度发育不良、高度发育不良和腺癌中,TP53 改变的发生率分别为 71%、83%和 100%。SEC 和相关肿瘤的配对测序显示,3 名患者的 TP53 错义突变相同。相比之下,91%的无发育不良/肿瘤的 SSL 样/SL-NOS 标本含有 KRAS/BRAF 突变,这些突变在相关低度发育不良中保持不变。在 SEC 或 SSL 样/SL-NOS 患者的未受影响的粘膜中均未发现基因组改变。根据我们的发现,我们得出结论,SEC 与 IBD 患者的 SSL 样锯齿状结直肠病变不同,是 IBD 相关肿瘤的早期前体,需要结肠镜监测。