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Tumour biology and histopathology of neuroendocrine tumours.

Author information

1
Department of Pathology, University of Kiel, Michaelisstr. 11, 24105 Kiel, Germany. guenterkloeppel@path.uni-kiel.de

Abstract

The tumours of the disseminated/diffuse neuroendocrine cell system are a group of neoplasms sharing uniformly appearing cells which differ from each other in their biology, prognosis and genetics. In the lung they are called carcinoid and small/large-cell neuroendocrine carcinomas. In the gastroenteropancreatic compartment they are classified as well-differentiated neuroendocrine tumours or carcinomas and poorly differentiated neuroendocrine carcinomas. Depending on their localization these neoplasms reveal distinct phenotypes with respect to pathology, immunohistochemistry, and hormonal syndromes. Their clinical behaviour--ranging from benign and low-grade to high-grade malignancy--can be predicted on the basis of clinicopathological criteria. Currently extensive work is being performed to unravel the genetic background.

PMID:
17382263
DOI:
10.1016/j.beem.2007.01.004
[Indexed for MEDLINE]

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