Department of Medicine (DIMED), Surgical Pathology & Cytopathology Unit, University of Padova, Italy.
Dig Liver Dis. 2013 Mar;45(3):186-94. doi: 10.1016/j.dld.2012.07.013. Epub 2012 Sep 10.
In both Crohn's disease and ulcerative colitis, the secondary prevention of colorectal cancer basically relies on the histological detection of dysplasia. In inflammatory bowel diseases, dysplasia identifies the subgroup of patients eligible for stricter surveillance (or prophylactic colectomy). In clinical practice, a number of issues may influence the benefits of clinico-pathological surveillance for inflammatory bowel disease patients with dysplasia, including: sampling errors, inconsistent biopsy assessments, patients' compliance with follow-up requirements, and how heath care is organized. Even in such a multifaceted context, it has been demonstrated that dysplasia surveillance is effective in reducing colorectal cancer-related mortality and morbidity. This paper focuses on current issues concerning the histological assessment of inflammatory bowel disease-associated dysplastic lesions.
在克罗恩病和溃疡性结肠炎中,结直肠癌的二级预防基本上依赖于对异型增生的组织学检测。在炎症性肠病中,异型增生确定了适合更严格监测(或预防性结肠切除术)的患者亚组。在临床实践中,有许多问题可能会影响异型增生的炎症性肠病患者的临床病理监测的获益,包括:采样误差、不一致的活检评估、患者对随访要求的依从性以及医疗保健的组织方式。即使在这种多方面的情况下,也已经证明异型增生监测可有效降低结直肠癌相关的死亡率和发病率。本文重点介绍了与炎症性肠病相关的异型增生病变的组织学评估的当前问题。