Literature DB >> 31359091

[Neuroendocrine tumors : Classification, clinical presentation and imaging].

H Scherübl1, F Raue2, K Frank-Raue2.   

Abstract

CONTEXT: Neuroendocrine tumors (NET) are a heterogeneous group of neoplasms found in all organs. They often present with characteristic clinical syndromes due to hormone hypersecretion. DIAGNOSTICS: In addition to hormone diagnostics molecular-genetic work-up can play an important role. IMAGING: Morphological imaging comprises ultrasound, endoscopy, computed tomography (CT) and magnetic resonance imaging (MRI) scans. Functional imaging of NET relies on radioligands that bind to specific receptors or transporters (Ga-68-DOTATATE-PET-CT, Tc-99-tektrotyd-SPECT/CT, F‑18-DOPA-PET/CT). THERAPY: Somatostatin analogs either native or coupled to radionuclides are potent drugs for treating various neuroendocrine tumors.
CONCLUSION: The requirements of imaging are determined by clinical presentation, laboratory findings, tumor stage, the presence of a tumor syndrome and the need of a personalized systemic treatment modality.

Entities:  

Keywords:  Gastroenteropancreatic neuroendocrine tumors; Imaging; Medullary thyroid cancer; Pheochromocytoma; Pituitary adenoma

Mesh:

Substances:

Year:  2019        PMID: 31359091     DOI: 10.1007/s00117-019-0574-x

Source DB:  PubMed          Journal:  Radiologe        ISSN: 0033-832X            Impact factor:   0.635


  21 in total

Review 1.  Pulmonary neuroendocrine (carcinoid) tumors: European Neuroendocrine Tumor Society expert consensus and recommendations for best practice for typical and atypical pulmonary carcinoids.

Authors:  M E Caplin; E Baudin; P Ferolla; P Filosso; M Garcia-Yuste; E Lim; K Oberg; G Pelosi; A Perren; R E Rossi; W D Travis
Journal:  Ann Oncol       Date:  2015-02-02       Impact factor: 32.976

2.  Response to initial therapy predicts clinical outcomes in medullary thyroid cancer.

Authors:  Susan C Lindsey; Ian Ganly; Frank Palmer; R Michael Tuttle
Journal:  Thyroid       Date:  2014-11-24       Impact factor: 6.568

3.  [Practice guideline neuroendocrine tumors - AWMF-Reg. 021-27].

Authors: 
Journal:  Z Gastroenterol       Date:  2018-06-11       Impact factor: 2.000

Review 4.  Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas.

Authors:  Rodrigo A Toledo; Nelly Burnichon; Alberto Cascon; Diana E Benn; Jean-Pierre Bayley; Jenny Welander; Carli M Tops; Helen Firth; Trish Dwight; Tonino Ercolino; Massimo Mannelli; Giuseppe Opocher; Roderick Clifton-Bligh; Oliver Gimm; Eamonn R Maher; Mercedes Robledo; Anne-Paule Gimenez-Roqueplo; Patricia L M Dahia
Journal:  Nat Rev Endocrinol       Date:  2016-11-18       Impact factor: 43.330

5.  Neuroendocrine Tumors of the Gastrointestinal Tract.

Authors:  Detlef K Bartsch; Hans Scherübl
Journal:  Visc Med       Date:  2017-10-16

Review 6.  [Pulmonary neuroendocrine tumors in the new WHO 2015 classification: Start of breaking new grounds?].

Authors:  P A Schnabel; K Junker
Journal:  Pathologe       Date:  2015-05       Impact factor: 1.011

Review 7.  Pathohistological classification of pituitary tumors: 10 years of experience with the German Pituitary Tumor Registry.

Authors:  Wolfgang Saeger; Dieter K Lüdecke; Michael Buchfelder; Rudolf Fahlbusch; Hans-Jürgen Quabbe; Stephan Petersenn
Journal:  Eur J Endocrinol       Date:  2007-02       Impact factor: 6.664

Review 8.  Hereditary Medullary Thyroid Cancer Genotype-Phenotype Correlation.

Authors:  Karin Frank-Raue; Friedhelm Raue
Journal:  Recent Results Cancer Res       Date:  2015

Review 9.  Long-Term Follow-up in Medullary Thyroid Carcinoma.

Authors:  Friedhelm Raue; Karin Frank-Raue
Journal:  Recent Results Cancer Res       Date:  2015

Review 10.  Update of Pheochromocytoma Syndromes: Genetics, Biochemical Evaluation, and Imaging.

Authors:  Rami Alrezk; Andres Suarez; Isabel Tena; Karel Pacak
Journal:  Front Endocrinol (Lausanne)       Date:  2018-11-27       Impact factor: 5.555

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.