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209 例胃神经内分泌肿瘤的组织学特征及预后评估的改善。

Histologic characterization and improved prognostic evaluation of 209 gastric neuroendocrine neoplasms.

机构信息

Department of Pathology, Ospedale di Circolo, 21100 Varese, Italy.

出版信息

Hum Pathol. 2011 Oct;42(10):1373-84. doi: 10.1016/j.humpath.2011.01.018. Epub 2011 May 4.

Abstract

Gastric neuroendocrine neoplasms differ considerably in histology, clinicopathologic background, stage, and patient outcome, implying a wide spectrum of therapeutic options, hence the need for improved diagnostic and prognostic criteria to select appropriate therapy. Here, we tested the European NeuroEndocrine Tumor Society and the novel World Health Organization 2010 grade and stage classifications together with additional clinicopathologic and histologic parameters in a series of 209 gastric neuroendocrine neoplasms with a median follow-up of 89 months. Fifty-one grade 3 neuroendocrine carcinomas and 15 mixed endocrine-exocrine carcinomas of poor outcome were separated from 143 neuroendocrine tumors, including 132 G1 or G2 enterochromaffin-like (ECL) cell neoplasms and 11 G1 gastrin-cell, somatostatin-cell, or serotonin-cell tumors. Most G1 cases had excellent prognosis, even when metastatic, whereas G2 and G3 neoplasms had worse or very severe prognosis, respectively. The European NeuroEndocrine Tumor Society-World Health Organization 2010 proliferative grading system well correlated with patient survival. Structural histologic parameters were equally predictive and when combined with the European NeuroEndocrine Tumor Society-World Health Organization 2010 grading system in a "global grade" improved tumor prognostic stratification. The European NeuroEndocrine Tumor Society-World Health Organization 2010 staging system proved effective. Introduction of novel T (T(1a) and T(1b) or deep submucosal) and N categories (N(1), <3 nodes metastases; N(2), ≥3) allowed a simplified, equally informative 3-stage TNM system. Such improved diagnostic and prognostic criteria for gastric neuroendocrine neoplasms are proposed and discussed.

摘要

胃神经内分泌肿瘤在组织学、临床病理背景、分期和患者预后方面存在显著差异,这意味着存在广泛的治疗选择,因此需要改进诊断和预后标准,以选择合适的治疗方法。在这里,我们在一系列 209 例胃神经内分泌肿瘤中测试了欧洲神经内分泌肿瘤学会和新型世界卫生组织 2010 年分级和分期分类,以及另外的临床病理和组织学参数,中位随访时间为 89 个月。从 143 例神经内分泌肿瘤中分离出 51 例 3 级神经内分泌癌和 15 例预后不良的混合内分泌-外分泌癌,包括 132 例 G1 或 G2 肠嗜铬样(ECL)细胞肿瘤和 11 例 G1 胃泌素细胞、生长抑素细胞或 5-羟色胺细胞肿瘤。大多数 G1 病例即使转移也有极好的预后,而 G2 和 G3 肿瘤的预后分别较差或非常严重。欧洲神经内分泌肿瘤学会-世界卫生组织 2010 年增殖分级系统与患者生存情况密切相关。结构组织学参数同样具有预测性,当与欧洲神经内分泌肿瘤学会-世界卫生组织 2010 年分级系统结合在一个“总体分级”中时,可以改善肿瘤的预后分层。欧洲神经内分泌肿瘤学会-世界卫生组织 2010 年分期系统是有效的。引入新型 T(T1a 和 T1b 或深层黏膜下)和 N 分类(N1,<3 个淋巴结转移;N2,≥3 个)允许简化、同样信息丰富的 3 期 TNM 系统。因此,提出并讨论了胃神经内分泌肿瘤的这些改进的诊断和预后标准。

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