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从 EGFR/PTEN 共突变肺腺癌到淋巴结转移的小细胞癌的转化。

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

机构信息

Department of Human Pathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.

Department of General Thoracic Surgery, Graduate School of Medicine, Juntendo University, Tokyo, Japan.

出版信息

Pathol Int. 2020 May;70(5):295-299. doi: 10.1111/pin.12919. Epub 2020 Mar 12.

Abstract

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.

摘要

在未接受表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗的情况下,EGFR 突变型肺腺癌向小细胞肺癌(SCLC)转化的证据很少。在此,我们报告了一例伴有淋巴结转移的 EGFR/PTEN 共突变肺腺癌,其由腺癌与 SCLC 混合而成。原发肿瘤和淋巴结转移之间存在 EGFR L858R 和 PTEN R130Q 突变。此外,淋巴结转移中腺癌和 SCLC 成分之间存在 EGFR I744M 突变,证实了腺癌向 SCLC 的自发转化。此外,TP53 和 RB1 突变仅在淋巴结转移的 SCLC 成分中检测到。免疫组化显示,SCLC 中 Rb 表达完全缺失,提示 RB1 功能丧失。我们的病例清楚地表明,在没有 TKI 介导的进化选择压力的情况下,EGFR/PTEN 共突变肺腺癌在淋巴结中向 SCLC 转化。

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