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Pathologic staging of pancreatic, ampullary, biliary, and gallbladder cancers: pitfalls and practical limitations of the current AJCC/UICC TNM staging system and opportunities for improvement

机译:胰腺癌,壶腹癌,胆汁癌和胆囊癌的病理分期:当前AJCC / UICC TNM分期系统的陷阱和实际局限性以及改进的机会

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摘要

Tumors of the ampulla-pancreatobiliary tract are encountered increasingly; however, their staging can be highly challenging due to lack of familiarity. In this review article, the various issues encountered in staging of these tumors at the pathologic level are evaluated and possible solutions for daily practice as well as potential improvements for future staging protocols are discussed. While N-stage parameters have now been well established (the number of lymph nodes required in pancreatoduodenectomies is 12), the T-staging has several issues: for the pancreas, the discovery of small cancers arising in intraductal papillary mucinous neoplasms (IPMNs) and mucinous cystic neoplasms (MCNs) necessitates the creation of substages of T1 (as T1a, b, and c); lack of proper definition of "peripancreatic soft tissue" and "common bile duct involvement" (as to which part is meant) makes T3 highly subjective. Increasing resectability of main vessels (portal vein) brings the need to redefine a "T" for such cases. For the ampulla, due to factors like anatomic complexity of the region and the under-appreciation of three-dimensional spread of the tumors in this area (in particular, the frequent extension into periduodenal soft tissues and duodenal serosa, which are not addressed in the current system and which require specific grossing approaches to document), the current T-staging lacks reproducibility and clinical relevance, and therefore, major revisions are needed. Recently proposed refined definition and site-specific subclassification of ampullary tumors highlight the areas for improvement. For the extrahepatic bile ducts, the staging schemes that use the depth of invasion may be more practical to circumvent the inconsistencies in the histologic layering of the ducts; better definition of terms like "periductal spread" is needed. For the gallbladder, since many gallbladder cancers are "unapparent" (found in clinically and grossly unsuspected cholecystectomies), establishing proper grossing protocols and adequate sampling are crucial. Since the
机译:壶腹-胰腺胆道肿瘤越来越多。但是,由于缺乏熟悉度,他们的分期可能会非常具有挑战性。在这篇综述文章中,对这些肿瘤在病理水平上分期遇到的各种问题进行了评估,并讨论了日常实践的可能解决方案以及未来分期方案的潜在改进。虽然现在已经很好地确定了N阶段参数(胰十二指肠切除术所需的淋巴结数目为12),但T阶段存在几个问题:对于胰腺,发现在导管内乳头状黏液性肿瘤(IPMN)中产生的小癌和粘液性囊性肿瘤(MCN)需要创建T1的子阶段(如T1a,b和c); T3缺乏正确的定义,“胰周软组织”和“胆总管受累”(指的是哪个部分)使T3具有很高的主观性。主要血管(门静脉)的可切除性不断提高,因此有必要重新定义“ T”形。对于壶腹而言,由于该区域的解剖学复杂性和该区域肿瘤的三维扩散的认识不足等因素(特别是频繁扩展到十二指肠周软组织和十二指肠浆膜中,这在本节中并未解决)。当前的系统,并且需要使用特定的总收入方法进行记录),当前的T分期缺乏可重复性和临床相关性,因此需要进行重大修订。最近提出的壶腹肿瘤的改良定义和部位特异性亚分类突出了需要改进的领域。对于肝外胆管,采用浸润深度的分期方案可能更实用,可以规避导管组织学分层的不一致性。需要更好地定义诸如“周扩散”的术语。对于胆囊来说,由于许多胆囊癌是“不明显的”(在临床上和完全未曾怀疑的胆囊切除术中发现),因此建立适当的肉眼观察方案和充分的采样至关重要。自从

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