Article ; Online: Gastroenteropankreatische neuroendokrine Tumoren.
2021 Volume 61, Issue 12, Page(s) 1129–1138
Abstract: Neuroendocrine tumors (NET), or more generally neuroendocrine neoplasms (NEN), represent a very heterogeneous group of rare tumors with varying location which are only defined by their endocrine biology and secretion of synaptophysin and chromogranin A. ... ...
Title translation | Gastroenteropancreatic neuroendocrine tumors. |
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Abstract | Neuroendocrine tumors (NET), or more generally neuroendocrine neoplasms (NEN), represent a very heterogeneous group of rare tumors with varying location which are only defined by their endocrine biology and secretion of synaptophysin and chromogranin A. They originate from mesoderm-derived stem cells. In the last few years, the incidence and prevalence of NEN have been steadily increasing. Classification is based on the affected organ, the proliferation rate and presence or absence of hormone production with typical symptoms. Diagnosis and treatment of these tumors is therefore very specific and requires an interdisciplinary approach. Treatment options include endoscopic or surgical resection, drug therapy for control of symptoms and proliferation, locoregional therapy and radionuclide therapy. Guidelines with algorithms for diagnostic workup and treatment are constantly updated. |
MeSH term(s) | Humans ; Intestinal Neoplasms/diagnostic imaging ; Intestinal Neoplasms/therapy ; Neuroendocrine Tumors/diagnostic imaging ; Neuroendocrine Tumors/therapy ; Pancreatic Neoplasms/diagnostic imaging ; Pancreatic Neoplasms/therapy ; Stomach Neoplasms/diagnostic imaging ; Stomach Neoplasms/therapy |
Language | German |
Publishing date | 2021-11-02 |
Publishing country | Germany |
Document type | Journal Article |
ZDB-ID | 505520-9 |
ISSN | 1432-2102 ; 0033-832X |
ISSN (online) | 1432-2102 |
ISSN | 0033-832X |
DOI | 10.1007/s00117-021-00929-w |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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