Journal
AMERICAN JOURNAL OF CLINICAL PATHOLOGY
Volume 131, Issue 5, Pages 694-700Publisher
OXFORD UNIV PRESS INC
DOI: 10.1309/AJCPBS85VJEOBPDO
Keywords
Micropapillary adenocarcinoma; Papillary adenocarcinoma; Bronchioloalveolar adenocarcinoma
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Micropapillary lung adenocarcinoma (MPA) has been reported as an aggressive variant of adenocarcinoma, frequently manifesting at high stage with a poor prognosis. We analyzed the clinical and molecular profile of 15 primary MPAs for K-ras, EGFR, and BRAF mutations and performed,fluorescence in situ hybridization for EGFR amplification. In our study, 11 (73%) of 75 MPAs harbored mutually exclusive mutations: 5 (33%) K-ras, 3 (20%) EGFR, and 3 (20%) BRA F. Mutations in all 3 genes occurred inpatients with a smoking history and tumors with mucinous differentiation and secondary lepidic, acinar, and solid growth, suggesting that in a Western population, cytomorphologic correlation with genetic mutations is more unpredictable than in Japanese cohorts. We conclude that K-ras, EGFR, and BRAF mutations are disproportionately seen in adenocarcinomas of lung with a dominant micropapillary growth pattern compared with conventional adenocarcinoma in our institutional experience.
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