Okubo Yoichiro, Motohashi Osamu, Nakayama Norisuke, Nishimura Ken, Kasajima Rika, Miyagi Yohei, Shiozawa Manabu, Yoshioka Emi, Suzuki Masaki, Washimi Kota, Kawachi Kae, Nito Madoka, Kameda Yoichi, Yokose Tomoyuki
Department of Pathology, Kanagawa Cancer Center, 2-3-2, Nakao, Asahi-Ku, Yokohama, Kanagawa, 241-8515, Japan.
Department of Gastroenterology, Kanagawa Cancer Center, 2-3-2, Nakao, Asahi-Ku, Yokohama, Kanagawa, 241-8515, Japan.
Diagn Pathol. 2016 Nov 8;11(1):128. doi: 10.1186/s13000-016-0580-5.
As the World Health Organization grading system for gastroenteropancreatic-neuroendocrine tumors (GEP-NETs) may not always correlate with tumor progression, it is imperative that other independent predictors of tumor progression be established. To identify such predictors, we conducted a retrospective histopathological study of hindgut NETs, obtained from endoscopic procedures, and used statistical analyses to evaluate predictive factors.
We first obtained clinicopathological data of cases of hindgut NETs. Tissue sections from tumor samples were prepared and subjected to pathological examination. In particular, we calculated the microvessel density (MVD) and lymphatic microvessel density (LMVD) values, and performed appropriate statistical analyses.
A total of 42 cases of hindgut NETs were selected for the study, 41 from the rectum and 1 from the sigmoid colon. Based on the Ki-67 labeling index, 34 cases were classified as NET G1 tumors and 8 as NET G2 tumors. MVD values ranged from 1.4/mm to 73.9/mm and LMVD values from 0/mm to 22.9/mm. MVD and LMVD were identified as risk factors for venous and lymphatic invasion of hindgut NETs. Moreover, MVD positively correlated with the maximum diameter of the tumor.
Tumor progression of NETs may cause angiogenesis and lymphangiogenesis, via an unknown mechanism, as well as lymphovascular invasion. Angiogenesis likely plays an important role in occurrence and progression in the initial phase of hindgut NETs.
由于世界卫生组织对胃肠胰神经内分泌肿瘤(GEP-NETs)的分级系统可能并不总是与肿瘤进展相关,因此必须建立其他独立的肿瘤进展预测指标。为了确定此类预测指标,我们对通过内镜检查获得的后肠神经内分泌肿瘤进行了回顾性组织病理学研究,并使用统计分析来评估预测因素。
我们首先获取了后肠神经内分泌肿瘤病例的临床病理数据。制备肿瘤样本的组织切片并进行病理检查。特别是,我们计算了微血管密度(MVD)和淋巴管微血管密度(LMVD)值,并进行了适当的统计分析。
总共选择了42例后肠神经内分泌肿瘤进行研究,其中41例来自直肠,1例来自乙状结肠。根据Ki-67标记指数,34例被分类为NET G1肿瘤,8例为NET G2肿瘤。MVD值范围为1.4/mm至73.9/mm,LMVD值范围为0/mm至22.9/mm。MVD和LMVD被确定为后肠神经内分泌肿瘤静脉和淋巴管侵犯的危险因素。此外,MVD与肿瘤的最大直径呈正相关。
神经内分泌肿瘤的肿瘤进展可能通过未知机制导致血管生成和淋巴管生成以及淋巴管侵犯。血管生成可能在后肠神经内分泌肿瘤初始阶段的发生和进展中起重要作用。