Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Dec;61(12):1129-1138.
doi: 10.1007/s00117-021-00929-w.

[Gastroenteropancreatic neuroendocrine tumors]

[Article in German]
Affiliations

[Gastroenteropancreatic neuroendocrine tumors]

[Article in German]
Nada Rayes et al. Radiologe. 2021 Dec.

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.

Der Begriff „neuroendokrine Tumoren“ (NET), oder allgemeiner „neuroendokrine Neoplasien“ (NEN), umfasst eine sehr heterogene Gruppe seltener Tumoren mit unterschiedlicher Dignität und Lokalisation, die allein durch ihre endokrine Biologie mit Ausbildung und Sekretion von Synaptophysin und/oder Chromogranin A definiert sind. Sie entwickeln sich aus mesodermalen Stammzellen. In den letzten Jahren sind Inzidenz und Prävalenz der NEN stetig gestiegen. Die Einteilung erfolgt nach betroffenem Organ, Proliferationsverhalten und möglichem Vorhandensein einer Hormonproduktion mit dann meist typischer Klinik. Diagnostik und Therapie der NEN sind deshalb sehr spezifisch und sollten interdisziplinär abgestimmt werden. Die Therapie umfasst die endoskopische oder chirurgische Resektion, eine medikamentöse Therapie zur Symptom- und Proliferationskontrolle, lokoregionäre Therapien und die Radionuklidtherapie. Dafür gibt es Leitlinien mit Therapiealgorithmen, die ständig aktualisiert werden.

Keywords: Chromogranin A; Neuroendocrine tumors/registries; Neuroendocrine tumors/treatment algorithms; Peptide receptor radionuclide therapy; Receptors, somatostatin.

PubMed Disclaimer

References

Literatur

    1. Yao JC, Hassan M, Phan A, Dagohoy C et al (2008) One hundred years after „carcinoid“: epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States. J Clin Oncol 26:3063–3072 - DOI
    1. Rindi G, Arnold R, Bosman FT et al (2010) Nomenclature and classification of neuroendocrine neoplasms of the digestive system. In: Bosman FT, Hruban RH, Theise ND (Hrsg) WHO classification of tumours of the digestive tract. IARC, Lyon, S 13–14
    1. Pape UF, Jann H, Müller-Norhorn J et al (2008) Prognostic relevance of a novel TNM classification system for upper gastroenteropancreatic neuroendocrine tumours. Cancer 113:256–265 - DOI
    1. Rindi G, Klöppel G, Coulevard A, Komminoth O et al (2007) TNM staging of midgut and hindgut neuroendocrine tumors: a consensus proposal including a grading system. Virchows Arch 451:757–762 - DOI
    1. Jensen RT et al (2008) Inherited pancreatic endocrine tumor syndromes: advances in molecular pathogenesis, diagnosis, management, and controversies. Cancer 113(Suppl 7):1807–1843 - DOI

MeSH terms

LinkOut - more resources