Li Bin, Lu Jing Chen, He Dan, Wang Jun, Zhou Hui, Shen Liangfang, Zhang Chunfang, Duan Chaojun
Institute of Medical Sciences, Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China ; Division of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China.
Division of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China.
Oncol Lett. 2014 Aug;8(2):589-593. doi: 10.3892/ol.2014.2169. Epub 2014 May 22.
Peritoneal carcinomatosis from lung cancer is rare, particularly from lung squamous cell carcinoma (LSCC). Concurrent somatic BRAF and KRAS mutations within the same tumor specimen have not been reported. The present study describes the case of a treatment-naïve LSCC patient with coexisting BRAF V600E and oncogenic KRAS G12A mutations in the primary lung lesion and the peritoneal metastases. The patient presented with prominent peritoneal carcinomatosis and an eosinophilic leukemoid reaction, but no respiratory symptoms. The patient succumbed 8 days after the onset of the condition due to rapid aggravation of the peritoneal carcinomatosis. To the best of our knowledge, this is the first study concerning the coexistence of BRAF and KRAS mutations in LSCC. Intensive activation of ERK was also observed in the primary lung lesion and the peritoneal metastases. Although the exact pathogenesis was unclear, the observations indicated that in the present study, the BRAF V600E and KRAS G12A mutations may have cooperate in inducing the malignant phenotype of LSCC. This case also highlighted the potential aggressive course and unusual pattern of spread of this specific dual-mutated tumor.
肺癌引起的腹膜癌罕见,尤其是肺鳞状细胞癌(LSCC)导致的。同一肿瘤标本中同时存在BRAF和KRAS体细胞突变的情况尚未见报道。本研究描述了1例未经治疗的LSCC患者,其原发性肺病变及腹膜转移灶中同时存在BRAF V600E和致癌性KRAS G12A突变。该患者表现为显著的腹膜癌和嗜酸性粒细胞类白血病反应,但无呼吸道症状。患者在病情发作8天后因腹膜癌迅速加重而死亡。据我们所知,这是第一项关于LSCC中BRAF和KRAS突变共存的研究。在原发性肺病变和腹膜转移灶中也观察到ERK的强烈激活。尽管确切的发病机制尚不清楚,但这些观察结果表明,在本研究中,BRAF V600E和KRAS G12A突变可能协同诱导了LSCC的恶性表型。该病例还凸显了这种特定双突变肿瘤潜在的侵袭性病程和不寻常的扩散模式。