医学
神经内分泌肿瘤
肺
肺癌
多学科团队
类癌
入射(几何)
肿瘤科
类癌综合征
内科学
病理
化疗
类癌
护理部
物理
光学
作者
Natalie Prinzi,Roberta Elisa Rossi,Claudia Proto,Giovanni Leuzzi,Alessandra Raimondi,Martina Torchio,Massimo Milione,Francesca Corti,Elena Colombo,Michele Prisciandaro,Tommaso Cascella,Carlo Spreafico,Teresa Beninato,Jorgelina Coppa,Giuseppe Lo Russo,Maria Di Bartolomeo,Filippo de Braud,Sara Pusceddu
标识
DOI:10.1016/j.cllc.2020.12.004
摘要
Neuroendocrine neoplasms of the lung represent about 20% to 30% of all neuroendocrine tumors. On the basis of clinical and pathologic characteristics, 2 different categories of tumors may be defined: poorly differentiated neuroendocrine neoplasms, characterized by a high rate of recurrences and poor prognosis, and well-differentiated neuroendocrine neoplasms (typical carcinoids and atypical carcinoids), which generally display an indolent course. Lung carcinoids represent only 1% to 5% of all lung malignancies, but their incidence has significantly increased over the past 30 years. Surgery is the reference standard of treatment for lung carcinoids with locoregional disease. For advanced or unresectable lung carcinoids, several therapeutic options are available, but the choice should be shared within a multidisciplinary team to ensure optimal therapeutic outcomes. We describe the current management of these rare neoplasms.
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