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Updated: Jul 11, 2025

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全面的下一代测序揭示了双重原发性结直肠癌被诊断成像遗漏:一个病例报告

Yan-Jun Qu¹, Qian-Shi Zhang², Bo Wang²

¹Department of Medical Oncology, The Second Hospital of Dalian Medical University, Dalian 116023, Liaoning Province, China.

World journal of gastrointestinal oncology

|November 16, 2023

概括

下一代测序 (NGS) 有助于诊断罕见的多重原发性结直肠癌 (MPCC). 基因检测和串行血DNA分析对于MPCC中准确的诊断和监测治疗反应至关重要.

科学领域:

在瘤学瘤学.
基因组学就是基因组学.
分子诊断学分子诊断学

背景情况:

多重原发性结直肠癌 (MPCC) 存在诊断挑战,经常被误认为是转移性疾病.
组织病理学方法可能不足以区分MPCC与转移性病变.
下一代测序 (NGS) 为识别多种原发性癌症提供了一个强大的工具.

关键词:

案例报告案例报告这种药物是Cetuximab.多重原发性结直肠癌多重原发性结直肠癌.这是下一代测序.在RET的融合中,RET的融合.

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