Abstract

Background Morule-like component (MLC) was a rare structure in primary lung adenocarcinoma. We aimed to reveal the clinicopathological, radiological, immunohistochemical, and molecular features of lung adenocarcinoma with MLCs. Methods Twenty lung adenocarcinomas with MLCs were collected, and computed tomographic and histological documents were reviewed. Immunohistochemistry, targeted next-generation sequencing, and Sanger sequencing for β-catenin gene were performed. Results There were 9 lepidic adenocarcinomas, 8 acinar adenocarcinomas, 2 papillary adenocarcinomas, and 1 minimally invasive adenocarcinoma. Most patients (16/17) were shown a pure solid nodule, and 1 patient was shown a partly solid nodule on chest computed tomography (CT). Nine cases were accompanied with micropapillary components, and 3 were with cribriform components in which 2 suffered a worse prognosis. No significant association was found between the MCLs and the overall survival of lung adenocarcinoma (P = 0.109). The MLCs were often arranged in whorled or streaming patterns. The cells in MLCs showed syncytial and mild appearance. The MLCs were positive for E-cadherin, CK7, TTF-1, napsin-A, vimentin, and β-catenin (membrane), and negative for CK5/6, p40, p63, Synaptophysin, chromogranin A, and Cdx-2. EGFR mutation, ALK-EML4 fusion, HER2 amplification, and PIK3CA mutation were detected in 16 cases, 2 cases, 1 case, and 1 case, respectively. EGFR mutation was more frequent in adenocarcinomas with MLCs than those without MLCs (P = 0.040). β-catenin gene mutation was not detected in any patients. Conclusions MLC is often observed in the background of acinar, lepidic, and papillary adenocarcinomas. Lung adenocarcinomas with MLCs tend to appear as a solid mass on CT and harbor EGFR gene mutations. The micropapillary components and cribriform components may cause poor prognosis of lung adenocarcinomas with MLCs. Vimentin is always positive in MLCs, and it is a useful marker for the identification of MLCs.

Highlights

  • In the recent World Health Organization (WHO) classification of primary lung neoplasm, primary lung adenocarcinomas were subdivided into five subtypes and four uncommon variants depending on their architectural and cellular features [1]

  • The Morule-like component (MLC) are usually accompanied by lepidic, acinar, and papillary predominant lung adenocarcinomas

  • Lung adenocarcinoma with MLCs tend to appear as a solid mass on computed tomography (CT) images

Read more

Summary

Introduction

In the recent World Health Organization (WHO) classification of primary lung neoplasm, primary lung adenocarcinomas were subdivided into five subtypes (lepidic adenocarcinoma, papillary adenocarcinoma, micropapillary adenocarcinoma, acinar adenocarcinoma, and solid adenocarcinoma) and four uncommon variants (mucinous adenocarcinoma, colloid adenocarcinoma, fetal adenocarcinoma, and enteric adenocarcinoma) depending on their architectural and cellular features [1]. Lung adenocarcinoma combined with morule-like components (MLCs) is not mentioned in this edition. Fornelli et al first released a case of lung adenocarcinoma with MLCs in 2003 [2]. The morule is one of the most important histological characteristics of pulmonary blastoma and low-grade fetal adenocarcinoma [1]. Morule-like component (MLC) was a rare structure in primary lung adenocarcinoma. Twenty lung adenocarcinomas with MLCs were collected, and computed tomographic and histological documents were reviewed. MLC is often observed in the background of acinar, lepidic, and papillary adenocarcinomas. Lung adenocarcinomas with MLCs tend to appear as a solid mass on CT and harbor EGFR gene mutations. The micropapillary components and cribriform components may cause poor prognosis of lung adenocarcinomas with MLCs. Vimentin is always positive in MLCs, and it is a useful marker for the identification of MLCs

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call