| Literature DB >> 20659620 |
Shuji Murakami1, Tomoyuki Yokose, Haruhiro Saito, Yuji Sakuma, Shoichi Matsukuma, Chikako Hasegawa, Tetsuro Kondo, Fumihiro Oshita, Hiroyuki Ito, Masahiro Tsuboi, Haruhiko Nakayama, Youichi Kameda, Kazumasa Noda, Kouzo Yamada.
Abstract
The fusion gene EML4-ALK (echinoderm microtubule-associated protein-like 4 gene and the anaplastic lymphoma kinase gene) was recently identified as a novel genetic alteration in non-small-cell lung cancer. The clinicopathological features of EML4-ALK-positive adenocarcinoma are reported to include its high incidence in young, non-smoking patients, tumors that show distinct solid or acinar growth patterns with or without signet-ring cell histology, and its mutually exclusive occurrence with mutations in EGFR and KRAS. However, the clinical findings have not been well described. Here, we report a case of EML4-ALK-positive lung adenocarcinoma that showed multiple metachronous lesions on the pleura and pulmonary field, suspected to be a recurrence of lung adenocarcinoma after a 20-year disease-free interval. The slow clinical course may be characteristic of EML4-ALK-positive lung adenocarcinoma. Therefore, long-term observation of patients with EML4-ALK-positive lung adenocarcinomas is required after surgery. Copyright (c) 2010 Elsevier Ireland Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20659620 DOI: 10.1016/j.lungcan.2010.05.019
Source DB: PubMed Journal: Lung Cancer ISSN: 0169-5002 Impact factor: 5.705