[SERRATED COLORECTAL ADENOCARCINOMA].

A M Nechipay, K V Shishkin, M V Zobnina, L M Cherkasova, V A Krivopuskov
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引用次数: 0

Abstract

The aim: To present a clinical case of serrated colon adenocarcinoma. To demonstrate morphological and genetic features of these tumors and to determine their clinical management.

Key points: Described case shows diagnostics of serrated colon adenocarcinoma. A 67-year-old woman presented for colonoscopy because of long constipation besides abdominal pain and distention have appeared recently. Colonoscopy was performed and she was found to have a 3.0 x 3.0-cm tumor next to hepatic flexure and pedunculated 1.2x0.7 cm polyp in sigmoid colon (type lp according to Paris classification). Endoscopic biopsies of these lesions were consistent with serrated adenocarcinoma and tubulovillous adenoma with foci of severe dysplasia. Additional diagnostic methods revealed no distant metastases. Patient was under went right hemicolectomy with D3 lymphodissection, lesion in sigmoid colon was removed using snare with electrocautery. Final pathology revealed no residual tissue in margins and no malignant cells in removed lymph nodes. Genetic diagnostics by PCR found high level of microsatellite instability and positive CpG island methylator phenotype (CIMP+) in tumor tissue.

Conclusions: According to WHO classification serrated lesion are considered to have malignant potential. They serve as the precursors for approximately 10% to 15% of sporadic colorectal cancer developed through the serrated pathway. These tumors were named serrated adenocarcinoma and had special morphological criteria that allow us to differentiate them with colorectal adenocarcinomas developed through the traditional pathway. Serrated adenocarcinoma has high level of microsatellite instability and positive CpG island methylator phenotype (CIMP+). Presence of microsatellite instability in tumor determines its more favorable prognosis because of tumor immunogenicity. Besides this type of cancer is more often responding to therapy with fluoropyrimidines.

[锯齿状结直肠腺癌]。
目的:报告一例锯齿状结肠腺癌的临床病例。展示这些肿瘤的形态学和遗传学特征,并确定其临床管理。本病例诊断为锯齿状结肠腺癌。67岁妇女,因长期便秘,腹痛,腹胀,最近出现结肠镜检查。结肠镜检查发现肝屈曲旁3.0 × 3.0 cm肿瘤,乙状结肠有带蒂1.2 × 0.7 cm息肉(Paris分型lp)。这些病变的内窥镜活检符合锯齿状腺癌和管状绒毛状腺瘤,伴严重不典型增生灶。其他诊断方法未发现远处转移。患者行右侧半结肠切除术并D3淋巴清扫术,乙状结肠病变用圈套电切切除。最终病理显示边缘无残留组织,切除淋巴结无恶性细胞。PCR基因诊断发现肿瘤组织微卫星不稳定性高,CpG岛甲基化表型(CIMP+)阳性。结论:根据WHO的分类,锯齿状病变被认为具有恶性潜能。它们是大约10%到15%的散发性结直肠癌通过锯齿状通路发展的前体。这些肿瘤被命名为锯齿状腺癌,具有特殊的形态学标准,使我们能够将其与通过传统途径发展的结直肠腺癌区分开来。锯齿状腺癌具有高水平的微卫星不稳定性和阳性CpG岛甲基化表型(CIMP+)。肿瘤微卫星不稳定性的存在,决定了肿瘤免疫原性对其预后有利。此外,这种类型的癌症通常对氟嘧啶治疗有反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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