Department of Gastroenterology, MetroHealth Medical Center, Case Western Reserve University, Cleveland, OH, USA.
Department of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA.
Indian J Gastroenterol. 2024 Oct;43(5):905-915. doi: 10.1007/s12664-024-01621-2. Epub 2024 Jul 26.
Patients with inflammatory bowel disease (IBD) are at an increased risk of developing colitis-associated neoplasia (CAN), including colorectal cancer (CRC), through the inflammation-dysplasia-neoplasia pathway. Dysplasia is the most reliable, early and actionable marker for CAN in these patients. While such lesions are frequently encountered, adequate management depends on an accurate assessment, complete resection and close surveillance. With recent advances in endoscopic technologies and research in the field of CAN, the management of dysplastic lesions has significantly improved. The American Gastroenterology Association and Surveillance for Colorectal Endoscopic Neoplasia Detection (SCENIC) provide a guideline framework for approaching dysplastic lesions in patients with IBD. However, there are significant gaps in these recommendations and real-world clinical practice. Accurate lesion assessment remains pivotal for adequate management of CAN. Artificial intelligence-guided modalities are now increasingly being used to aid the detection of these lesions further. As the lesion detection technologies are improving, our armamentarium of resection techniques is also expanding and includes hot or cold polypectomy, endoscopic mucosal resection, endoscopic sub-mucosal dissection and full-thickness resection. With the broadened scope of endoscopic resection, the recommendations regarding surveillance after resection has also changed. Certain patient populations such as those with invisible dysplasia or with prior colectomy and ileal pouch anal anastomosis need special consideration. In the present review, we aim to provide a state-of-the-art summary of the current practice of endoscopic detection, resection and surveillance of dysplasia in patients with IBD and provide some perspective on the future directions based on the latest research.
炎症性肠病(IBD)患者通过炎症-发育不良-肿瘤形成途径,发生结肠炎相关肿瘤(CAN),包括结直肠癌(CRC)的风险增加。发育不良是这些患者中 CAN 最可靠、最早和最具可操作性的标志物。尽管此类病变经常遇到,但适当的管理取决于准确的评估、完全切除和密切监测。随着内镜技术的最新进展和 CAN 领域的研究,对发育不良病变的管理得到了显著改善。美国胃肠病学会(AGA)和结直肠内镜肿瘤检测监测(SCENIC)为 IBD 患者中处理发育不良病变提供了指导框架。然而,这些建议和实际临床实践中存在重大差距。准确的病变评估仍然是 CAN 充分管理的关键。人工智能引导的模式现在越来越多地被用于辅助这些病变的检测。随着病变检测技术的不断提高,我们的切除技术手段也在不断扩大,包括热或冷息肉切除术、内镜黏膜切除术、内镜黏膜下剥离术和全层切除术。随着内镜切除范围的扩大,对切除后监测的建议也发生了变化。某些特定的患者群体,如那些有不可见发育不良或既往结肠切除术和回肠直肠吻合术的患者,需要特别考虑。在本综述中,我们旨在提供 IBD 患者内镜检测、切除和监测发育不良的最新实践的概述,并根据最新研究对未来方向提供一些观点。