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Clinicopathological characteristics and molecular analysis of primary pulmonary mucoepidermoid carcinoma: Case report and literature review

机译:原发性肺粘液表皮样癌的临床病理特征及分子分析:病例报告及文献复习

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摘要

Primary pulmonary mucoepidermoid carcinoma (PMEC) is extremely rare. Herein, we report a case of a 71‐year‐old male patient with high‐grade PMEC involving the right upper lobe that was successfully resected via lobectomy. As a result of invasion into the pleural and paratracheal lymph nodes, four cycles of adjuvant chemotherapy with paclitaxel and carboplatin were administered. There were no signs of relapse during 10 months of follow‐up. Furthermore, we reviewed the literature and summarized the surgical approaches, prognostic factors, and underlying genetic mechanisms of PMEC, which will benefit clinical treatment.
机译:原发性肺粘液表皮样癌(PMEC)极为罕见。本文中,我们报告了一名71岁男性高级别PMEC患者,其右上叶通过肺叶切除术成功切除。由于侵入胸膜和气管旁淋巴结,进行了四个周期的紫杉醇和卡铂辅助化疗。在随访的10个月内没有复发的迹象。此外,我们回顾了文献并总结了PMEC的手术方法,预后因素和潜在的遗传机制,这将有助于临床治疗。

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