Unit of Anatomic Pathology, Department of Molecular Medicine, University of Pavia and Fondazione IRCCS San Matteo Hospital, Via Carlo Forlanini 16 -, 27100, Pavia, Italy.
Pathology Unit, Department of Surgical and Diagnostic Sciences, University Hospital and Ospedale Policlinico San Martino IRCCS, Genova, Italy.
Virchows Arch. 2021 Oct;479(4):667-678. doi: 10.1007/s00428-021-03109-2. Epub 2021 May 8.
Most Crohn's disease-associated small bowel carcinomas (CrD-SBCs) are diagnosed in advanced stage and have poor prognosis. To improve diagnosis and therapy, a better knowledge of tumour precancerous lesions, histotypes and prognostic factors is needed. We investigated histologically and immunohistochemically 52 CrD-SBCs and 51 small bowel carcinomas unrelated to inflammatory disease, together with their tumour-associated mucosa, looking for Crohn-selective changes. Histologic patterns and phenotypic markers potentially predictive of CrD-SBC histogenesis and prognosis were analysed. Cytokeratin 7 or MUC5AC-positive metaplastic changes were found in about half of investigated CrD-SBCs, significantly more frequently than in CrD-unrelated SBCs. They correlated with metaplastic changes of their associated mucosa, while being absent in normal ileal mucosa. Histologic patterns suggestive for progression of some cytokeratin 7 and/or MUC5AC-positive metaplastic lesions into cancer of the same phenotype were also observed. Patient survival analyses showed that tumour cytokeratin 7 or MUC5AC expression and non-cohesive histotype were adverse prognostic factors at univariable analysis, while cytokeratin 7 and non-cohesive histotype were also found to predict worse survival in stage- and age-inclusive multivariable analyses. Besides conventional dysplasia, hyperplasia-like non-conventional lesions were observed in CrD-SBC-associated mucosa, with patterns suggestive for a histogenetic link with adjacent cancer. In conclusion the cytokeratin 7 and/or MUC5AC-positive metaplastic foci and the non-conventional growths may have a role in cancer histogenesis, while tumour cytokeratin 7 and non-cohesive histotype may also predict poor patient survival. Present findings are worth being considered in future prospective histogenetic and clinical studies.
大多数克罗恩病相关的小肠腺癌(CrD-SBC)在晚期诊断,预后较差。为了改善诊断和治疗,需要更好地了解肿瘤癌前病变、组织类型和预后因素。我们对 52 例 CrD-SBC 和 51 例与炎症性疾病无关的小肠腺癌进行了组织学和免疫组织化学研究,同时研究了它们的肿瘤相关黏膜,寻找克罗恩病特有的改变。分析了潜在预测 CrD-SBC 组织发生和预后的组织学模式和表型标志物。在大约一半的研究 CrD-SBC 中发现了角蛋白 7 或 MUC5AC 阳性的化生改变,明显多于 CrD 无关的 SBC。它们与相关黏膜的化生改变相关,而在正常回肠黏膜中不存在。还观察到一些角蛋白 7 和/或 MUC5AC 阳性化生病变向相同表型的癌症进展的组织学模式。患者生存分析表明,肿瘤角蛋白 7 或 MUC5AC 表达和非黏附组织学类型是单变量分析的不良预后因素,而角蛋白 7 和非黏附组织学类型在包括分期和年龄的多变量分析中也被发现预测更差的生存。除了传统的异型增生外,还观察到 CrD-SBC 相关黏膜中的增生样非传统病变,其形态提示与相邻癌症有组织发生联系。总之,角蛋白 7 和/或 MUC5AC 阳性的化生灶和非传统生长可能在癌症的组织发生中起作用,而肿瘤角蛋白 7 和非黏附组织学类型也可能预测患者预后不良。目前的发现值得在未来的前瞻性组织发生学和临床研究中考虑。