Semin Respir Crit Care Med 1997; 18(4): 405-415
DOI: 10.1055/s-2007-1009355
Copyright © 1997 by Thieme Medical Publishers, Inc.

Rare Pulmonary Neoplasms

Daniel L. Miller
  • Division of Cardiothoracic Surgery, University of Louisville School of Medicine, Louisville, Kentucky
Further Information

Publication History

Publication Date:
20 March 2008 (online)

Abstract

Rare primary neoplasms of the lung account for less than 1% of all primary lung cancers. These pulmonary tumors are usually metastatic. Accurate histopathologic studies and detailed clinical history are essential to confirm the diagnosis of unusual primary neoplasms of the lung. Rare pulmonary neoplasms are subdivided into six major histopathologic groups and include lymphoid tumors, soft tissue sarcomas, salivary gland tumors, mixed epithelial/mesenchymal tumors, ectopic tissue tumors, and undetermined histogenetic tumors. Surgical resection, when possible, is the treatment of choice for rare pulmonary neoplasms. The effects of adjuvant therapy on long-term survival and disease-free interval is not known because of the rarity of these neoplasms. Overall survival is better when compared with primary bronchogenic carcinoma. Therefore, aggressive surgical treatment of rare primary neoplasms of the lung is warranted.