阑尾神经内分泌肿瘤中肿瘤细胞亚型的临床病理学意义:135例肿瘤系列

IF 11.3 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Endocrine Pathology Pub Date : 2024-06-01 Epub Date: 2024-06-04 DOI:10.1007/s12022-024-09813-4
Ozgur Mete, David W Dodington, Daniel L Shen, Sylvia L Asa
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引用次数: 0

摘要

阑尾神经内分泌瘤(NET)很常见,通常是在阑尾切除术时偶然发现的病变。治疗指南以肿瘤大小、浸润程度和 Ki67 增殖指数为依据。大多数小肠NET由分泌羟色胺的EC细胞组成,但也有多种其他类型的神经内分泌细胞。直肠中存在表达肽 YY(PYY)、胰高血糖素样肽(GLPs)和胰多肽(PP)的 L 细胞肿瘤;它们被认为比分泌血清素的肿瘤预后更好。我们研究了阑尾是否存在基于细胞类型的不同神经内分泌肿瘤类型,以及这种区别是否具有临床意义。我们从多伦多UHN和克利夫兰UHCMC的病理档案中收集了135例阑尾NET。我们分析了 CDX2、SATB2、PSAP、5-羟色胺、胰高血糖素(可检测 GLPs)、PYY 和胰多肽(PP)等生物标志物的表达情况,并将分析结果与临床病理参数进行了关联。免疫组化确定了三种类型的阑尾 NET。其中75例(56%)被归类为EC细胞肿瘤,37例(27%)被归类为L细胞肿瘤;其余23例(17%)表达5-羟色胺和一种L细胞生物标记物,被归类为混合型。与 L 细胞肿瘤相比,EC 细胞肿瘤明显更大,侵袭范围更广,涉及固有肌、粘膜下和阑尾间质。混合瘤在所有这些参数上都处于中间水平。EC细胞肿瘤和混合瘤都有淋巴和/或血管侵犯,而L细胞肿瘤则没有。与EC细胞NET不同,L细胞肿瘤与淋巴结转移无关。肿瘤类型与pT分期相关,该系列中唯一有远处转移疾病的患者是EC细胞肿瘤。我们的研究证实,阑尾NET并不是一个单一的肿瘤群体。阑尾NET至少有三种类型,包括EC细胞瘤、L细胞瘤和混合瘤。这一信息对监测患者非常重要,因为监测尿液中的5HIAA水平只适用于分泌羟色胺的肿瘤患者,而测量GLPs和/或PP则更适用于L细胞肿瘤患者。我们的数据还显示,肿瘤类型具有重要意义,其中EC细胞肿瘤的侵袭性最强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Clinicopathological Significance of Tumor Cell Subtyping in Appendiceal Neuroendocrine Tumors: A Series of 135 Tumors.

The Clinicopathological Significance of Tumor Cell Subtyping in Appendiceal Neuroendocrine Tumors: A Series of 135 Tumors.

Appendiceal neuroendocrine tumors (NETs) are common and often are identified as incidental lesions at the time of appendectomy. The guidelines for management are based on tumor size, degree of invasion, and the Ki67 proliferation index. Most small bowel NETs are composed of serotonin-producing EC-cells, but there are multiple other neuroendocrine cell types. In the rectum, there are L-cell tumors that express peptide YY (PYY), glucagon-like peptides (GLPs), and pancreatic polypeptide (PP); they are thought to have a better prognosis than serotonin-producing tumors. We investigated whether the appendix has distinct neuroendocrine tumor types based on cell type and whether that distinction has clinical significance. We collected 135 appendiceal NETs from the pathology archives of UHN Toronto and UHCMC (Cleveland). We analyzed the expression of biomarkers including CDX2, SATB2, PSAP, serotonin, glucagon (that detects GLPs), PYY, and pancreatic polypeptide (PP) and correlated the results with clinicopathologic parameters. Immunohistochemistry identified three types of appendiceal NETs. There were 75 (56%) classified as EC-cell tumors and 37 (27%) classified as L-cell tumors; the remaining 23 (17%) expressed serotonin and one of the L-cell biomarkers and were classified as mixed. EC-cell tumors were significantly larger with more extensive invasion involving the muscularis propria, subserosa, and mesoappendix compared with L-cell tumors. Mixed tumors were intermediate in all of these parameters. Both EC-cell and mixed tumors had lymphatic and/or vascular invasion while L-cell tumors had none. Unlike EC-cell NETs, L-cell tumors were not associated with lymph node metastasis. Tumor type correlated with pT stage and the only patient with distant metastatic disease in this series had an EC-cell tumor. Our study confirms that appendiceal NETs are not a homogeneous tumor population. There are at least three types of appendiceal NET, including EC-cell, L-cell, and mixed tumors. This information is important for surveillance of patients, as monitoring urinary 5HIAA levels is only appropriate for patients with serotonin-producing tumors, whereas measurement of GLPs and/or PP is more appropriate for patients with L-cell tumors. Our data also show that tumor type is of significance with EC-cell tumors exhibiting the most aggressive behavior.

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来源期刊
Endocrine Pathology
Endocrine Pathology 医学-病理学
CiteScore
12.30
自引率
20.50%
发文量
41
审稿时长
>12 weeks
期刊介绍: Endocrine Pathology publishes original articles on clinical and basic aspects of endocrine disorders. Work with animals or in vitro techniques is acceptable if it is relevant to human normal or abnormal endocrinology. Manuscripts will be considered for publication in the form of original articles, case reports, clinical case presentations, reviews, and descriptions of techniques. Submission of a paper implies that it reports unpublished work, except in abstract form, and is not being submitted simultaneously to another publication. Accepted manuscripts become the sole property of Endocrine Pathology and may not be published elsewhere without written consent from the publisher. All articles are subject to review by experienced referees. The Editors and Editorial Board judge manuscripts suitable for publication, and decisions by the Editors are final.
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