[Non-small cell lung carcinoma with co-expression of TTF1 and p40: a clinicopathological analysis of six cases].

H S Liu, Y J Zhang, B Huang, H Y Ge, L B Cai, M M Chen
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Abstract

Objective: To investigate the clinicopathological features, molecular pathology characteristics, and prognosis of non-small cell lung carcinoma (NSCLC) exhibiting co-expression of p40 and thyroid transcription factor1 (TTF1). Methods: Clinical and pathological data of six NSCLC cases with co-expression of p40 and TTF1 diagnosed at the First People's Hospital of Xiaoshan District, Hangzhou, China from January 2016 to December 2023 were collected. Relevant literature was also reviewed. Results: NSCLC with co-expression of p40 and TTF1 commonly occurred in male smokers and had been in stage Ⅲ-Ⅳ when diagnosis. Microscopic examination revealed that the tumor cells were arranged in solid nests and sheets with marked atypia and visible mitotic figures. There was no prominent evidence of keratinization or glandular formation. The tumor cells diffusely co-expressed p40 and TTF1, exhibiting a dual immunophenotype characteristic of both squamous cell carcinoma and adenocarcinoma. Molecular testing of four NSCLC co-expressing p40 and TTF1 revealed the presence of common EGFR mutations, as well as mutations of NRAS (mutation rate of 2.09%), EML4-ALK (mutation rate of 24.77%), and PIK3CA (exon 10 c.1658 G>C p.S553T, mutation rate of 4.32%). All six tumors were poorly differentiated, highly invasive, and associated with poor prognosis. Four of the six patients experienced widespread metastasis and died within 7 to 30 months after the diagnosis or initial treatment. Conclusions: NSCLC with co-expression of p40 and TTF1 exhibits distinct clinicopathological features, immunophenotypes, molecular alterations, and clinical outcomes, characterized by rapid progression and poor prognosis. Pathologists should be vigilant in recognizing this entity to avoid misdiagnosis and missed diagnosis.

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[TTF1和p40共同表达的非小细胞肺癌:六例病例的临床病理分析]。
研究目的研究p40和甲状腺转录因子1(TTF1)共同表达的非小细胞肺癌(NSCLC)的临床病理特征、分子病理学特征和预后。研究方法收集2016年1月至2023年12月杭州市萧山区第一人民医院确诊的6例p40和TTF1共同表达的NSCLC病例的临床和病理资料。同时还查阅了相关文献。结果p40和TTF1共同表达的NSCLC常见于男性吸烟者,确诊时已处于Ⅲ-Ⅳ期。显微镜检查发现,肿瘤细胞呈实性巢状和片状排列,有明显的不典型性和可见的有丝分裂。没有明显的角化或腺体形成迹象。肿瘤细胞弥漫共表达 p40 和 TTF1,表现出鳞状细胞癌和腺癌的双重免疫表型特征。对四例共同表达 p40 和 TTF1 的 NSCLC 进行的分子检测显示,存在常见的表皮生长因子受体(EGFR)突变,以及 NRAS(突变率为 2.09%)、EML4-ALK(突变率为 24.77%)和 PIK3CA(外显子 10 c.1658 G>C p.S553T,突变率为 4.32%)突变。所有六种肿瘤均分化不良,侵袭性强,预后较差。六名患者中有四名出现广泛转移,并在确诊或初始治疗后 7 至 30 个月内死亡。结论p40和TTF1共同表达的NSCLC表现出不同的临床病理特征、免疫表型、分子改变和临床结局,其特点是进展快、预后差。病理学家在识别这一实体时应保持警惕,以避免误诊和漏诊。
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中华病理学杂志
中华病理学杂志 Medicine-Medicine (all)
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1.00
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0.00%
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10377
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