Journal article
Gastroenteropancreatic neuroendocrine tumours.
- Abstract:
-
Gastroenteropancreatic (GEP) neuroendocrine tumours (NETs) are fairly rare neoplasms that present many clinical challenges. They secrete peptides and neuroamines that cause distinct clinical syndromes, including carcinoid syndrome. However, many are clinically silent until late presentation with mass effects. Investigation and management should be highly individualised for a patient, taking into consideration the likely natural history of the tumour and general health of the patient. Manageme...
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- Publication status:
- Published
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- Publisher copy:
- 10.1016/s1470-2045(07)70410-2
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Authors
Bibliographic Details
- Journal:
- Lancet. Oncology
- Volume:
- 9
- Issue:
- 1
- Pages:
- 61-72
- Publication date:
- 2008-01-01
- DOI:
- EISSN:
-
1474-5488
- ISSN:
-
1470-2045
- Source identifiers:
-
15054
Item Description
- Language:
- English
- Keywords:
- Pubs id:
-
pubs:15054
- UUID:
-
uuid:14529d57-6583-432d-b58d-3dc81a442a66
- Local pid:
- pubs:15054
- Deposit date:
- 2012-12-19
Terms of use
- Copyright date:
- 2008
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