| Literature DB >> 33618994 |
Natalie Prinzi1, Roberta Elisa Rossi2, Claudia Proto3, Giovanni Leuzzi4, Alessandra Raimondi3, Martina Torchio3, Massimo Milione5, Francesca Corti3, Elena Colombo3, Michele Prisciandaro3, Tommaso Cascella6, Carlo Spreafico6, Teresa Beninato3, Jorgelina Coppa7, Giuseppe Lo Russo3, Maria Di Bartolomeo3, Filippo de Braud8, Sara Pusceddu3.
Abstract
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.Entities:
Keywords: Bronchial neuroendocrine tumors; Diagnosis; Epidemiology; Therapy; Typical carcinoid
Mesh:
Year: 2020 PMID: 33618994 DOI: 10.1016/j.cllc.2020.12.004
Source DB: PubMed Journal: Clin Lung Cancer ISSN: 1525-7304 Impact factor: 4.785