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Transformation from EGFR/PTEN EGFR/PTEN co‐mutated lung adenocarcinoma to small cell carcinoma in lymph node metastasis

机译:从EGFR / PTEN EGFR / PTEN共突变肺腺癌转化为淋巴结转移中的小细胞癌

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摘要

There is minimal evidence of EGFR ‐mutated lung adenocarcinoma transforming to small cell lung carcinoma (SCLC) without the administration of EGFR‐tyrosine kinase inhibitor (TKI). Here, we present a case of EGFR/PTEN co‐mutated lung adenocarcinoma with lymph node metastases, which comprised adenocarcinoma admixed with SCLC. EGFR L858R and PTEN R130Q mutations were shared between the primary tumor and lymph node metastasis. Additionally, EGFR I744M mutation was shared between the adenocarcinoma and SCLC components in the lymph node metastasis, confirming spontaneous transformation from adenocarcinoma to SCLC. Furthermore, TP53 and RB1 mutations were detected only in the SCLC components of the lymph node metastasis. Immunohistochemically, complete absence of Rb expression in SCLC was observed, suggesting the loss of function of RB1 . Our case clearly shows that EGFR/PTEN co‐mutated lung adenocarcinoma transformed to SCLC in the lymph node without TKI‐mediated evolutionary selection pressures.
机译:在没有施用EGFR-酪氨酸激酶抑制剂(TKI)的情况下,对小细胞肺癌(SCLC)转化的初步证据最小。这里,我们提出了具有淋巴结转移的EGFR / PTEN共突变肺腺癌的情况,其包括与SCLC混合的腺癌。在原发性肿瘤和淋巴结转移之间共享EGFR L858R和PTEN R130Q突变。另外,在淋巴结转移中的腺癌和SCLC组分之间共享EGFR I​​744M突变,确认从腺癌到SCLC的自发转化。此外,仅在淋巴结转移的SCLC组分中检测TP53和RB1突变。免疫组织化学,观察到SCLC中的完全没有RB表达,表明RB1的功能丧失。我们的案例清楚地表明,EGFR / PTEN共突变的肺腺癌在没有TKI介导的进化选择压力的情况下转化为SCLC。

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