| Literature DB >> 23891513 |
Gouji Toyokawa1, Mitsuhiro Takenoyama2, Kenichi Taguchi3, Katsumi Arakaki3, Eiko Inamasu1, Ryo Toyozawa1, Miyako Kojo1, Yoshimasa Shiraishi1, Yosuke Morodomi1, Tomoyoshi Takenaka1, Fumihiko Hirai1, Masafumi Yamaguchi1, Takashi Seto1, Alvaro Leone4, Paolo Graziano4, Yukito Ichinose1.
Abstract
Mutations of the epidermal growth factor receptor (EGFR) gene play a critical role in carcinogenesis of lung cancer, particularly adenocarcinoma. However, to the best of our knowledge, no mutations of the EGFR in patients with lung carcinosarcoma have been identified. We herein report the case of a 61-year-old female referred for a detailed examination of a left pulmonary mass shadow. Although bronchoscopy was performed, it failed to lead to a diagnosis, and video-assisted thoracoscopic surgery was therefore carried out to diagnose the tumor. The pathology revealed biphasic features consisting of both adenocarcinoma and chondrosarcoma. Intriguingly, both the adenocarcinoma and chondrosarcoma components were proven to harbor an exon19 deletion in the EGFR gene. Although carcinosarcoma is a rare malignancy of the lungs, genetic analyses of oncogenic drivers, such as the EGFR gene, should be conducted.Entities:
Keywords: EGFR-TKI; Epidermal growth factor receptor; Lung carcinosarcoma; Lung sarcomatoid carcinoma; Molecular-targeted therapy; Oncogenic drivers
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Year: 2013 PMID: 23891513 DOI: 10.1016/j.lungcan.2013.06.013
Source DB: PubMed Journal: Lung Cancer ISSN: 0169-5002 Impact factor: 5.705