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Neuroendocrine tumours of the lung

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Management of Rare Adult Tumours
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Abstract

Neuroendocrine tumours of the lung (NETL) are rare, representing some 20 % of lung tumours. This term groups different entities, covering a wide histological spectrum: typical (TC) and atypical (AC) carcinoid tumours, large cell neuroendocrine carcinomas (LCNEC) as well as small cell carcinomas (SCLC), the frequency of which is high (15% of lung tumours and nearly 80% of neuroendocrine tumours of the lung), the latter not described in this chapter. The clinical presentation and progressive profile of NETL are different and reflect a growing aggressiveness. The knowledge of the oncogenesis and natural history of these tumours has greatly evolved in recent years and the histological criteria that allow their individualisation have been refined; however, their rarity has as yet prevented the definition of an optimal treatment. Nonetheless, encouraging therapeutic prospects are creating renewed interest in clinical research on these little-known tumours.

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© 2009 Springer-Verlag France, Paris

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Bonnichon, A., Le Floch, H., Rivière, F., Margery, J., Vaylet, F. (2009). Neuroendocrine tumours of the lung. In: Belkacémi, Y., Mirimanoff, RO., Ozsahin, M. (eds) Management of Rare Adult Tumours. Springer, Paris. https://doi.org/10.1007/978-2-287-92246-6_48

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  • DOI: https://doi.org/10.1007/978-2-287-92246-6_48

  • Publisher Name: Springer, Paris

  • Print ISBN: 978-2-287-92245-9

  • Online ISBN: 978-2-287-92246-6

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