Matsukuma Susumu, Okada Kenji, Takeo Hiroaki, Sato Kimiya
Department of Pathology, Japan Self Defense Forces Central Hospital, Tokyo 154-0001, Japan.
Oncol Lett. 2012 Mar;3(3):689-693. doi: 10.3892/ol.2011.538. Epub 2011 Dec 23.
Cases of colo-ileal carcinoma (CIC), defined as intestinal carcinoma involving the right-sided colon and the ileum, are rarely encountered. The aim of this study was to elucidate the clinicopathological characteristics, which have been poorly understood, in such cases. A total of 16 CICs were examined histologically and immunohistochemically. Microsatellite instability-related histology was also evaluated according to previously published models, such as MsPath and PREDICT. CICs included 14 adenocarcinomas and 2 mucinous adenocarcinomas. The CICs showed focal or diffuse cytokeratin 20 expression and 7 CICs showed focal cytokeratin 7 co-expression. MsPath and PREDICT scores ranged from 1.6 to 6.6 (mean, 3.14) and from 1.6 to 7.8 (mean, 3.86), respectively. Three CICs showed loss of MLH1 immunoreactivity. Prominent neutrophilia and cancerous lymphangiosis in Peyer's patches (CLPP) were found in 8 cases (50%) and in 3 cases (18.8%), respectively. Neither variable was associated with parameters such as gender, tumor size or poor prognosis. However, the PREDICT score in prominently neutrophilic CICs was significantly higher than that in CICs with non-prominent neutrophilia (P=0.004). Patients with CLPP-positive CICs were significantly younger than those with CLPP-negative CICs (P=0.031). This study showed that almost all CICs originate from the right-sided colon with possible high levels of microsatellite instability. Prominent neutrophilia may be an additional histological indicator for microsatellite instability. Prognosis-independent CLPP occasionally occurs in younger patients with CICs.
结肠-回肠癌(CIC)病例,定义为累及右侧结肠和回肠的肠道癌,很少见。本研究的目的是阐明此类病例中尚未被充分了解的临床病理特征。对总共16例CIC进行了组织学和免疫组织化学检查。还根据先前发表的模型,如MsPath和PREDICT,评估了微卫星不稳定性相关组织学。CIC包括14例腺癌和2例黏液腺癌。CIC显示局灶性或弥漫性细胞角蛋白20表达,7例CIC显示局灶性细胞角蛋白7共表达。MsPath和PREDICT评分分别为1.6至6.6(平均3.14)和1.6至7.8(平均3.86)。3例CIC显示MLH1免疫反应性缺失。分别在8例(50%)和3例(18.8%)中发现派尔集合淋巴结显著嗜中性粒细胞增多和癌性淋巴管炎(CLPP)。这两个变量均与性别、肿瘤大小或预后不良等参数无关。然而,显著嗜中性粒细胞增多的CIC中的PREDICT评分显著高于非显著嗜中性粒细胞增多的CIC(P=0.004)。CLPP阳性的CIC患者明显比CLPP阴性的患者年轻(P=0.031)。本研究表明,几乎所有CIC起源于右侧结肠,可能具有高水平的微卫星不稳定性。显著嗜中性粒细胞增多可能是微卫星不稳定性的另一个组织学指标。与预后无关的CLPP偶尔发生在年轻的CIC患者中。