Neuroendocrine Tumors in Real Life

Neuroendocrine Tumors in Real Life

From Practice to Knowledge

Colao, Annamaria; de Herder, Wouter; Faggiano, Antongiulio

Springer International Publishing AG

06/2019

349

Mole

Inglês

9783319865348

15 a 20 dias

757

Descrição não disponível.
Part I General Remarks: Epidemiology of NET (by site of tumour and by geographical area).- Pathological classification (GEP, TNET and rare forms).-Biology of NET (oncogenes, tumor suppressor genes, epigenetics).- Part II Clinical Cases and Their Implications (from clinical practice to guidelines): Prognostic factors: TNM.- Grading (Ki67 score).- Molecular pathway - somatostatin receptors.- Molecular pathway - oncogene (mTOR).- Molecular pathway - tumor suppressor gene (MEN1).- Nuclear medicine imaging (FDG-PET).- Nuclear medicine imaging (Octreoscan / gallium PET).- Diagnosis: Tumor detection in syndromic NET (carcinoid syndrome).- Tumor detection in syndromic NET (ZES).- Tumor detection in syndromic NET (hypoglycemic hyperinsulinemic syndrome).- Tumor detection in incidentally detected non-functioning NET.- Tumor staging (stomach/duodenum, colon/rectum).- Tumor staging (bronchi).- Tumor staging (il

eum).- Tumor staging (pancreas).- Therapy: Locoregional disease (stomach).- Locoregional disease (pancreas).- Locoregional disease (ileum).- Locoregional disease (appendix).- Locoregional disease (bronchi).- Metastatic disease (stomach).- Metastatic disease (pancreas).- Metastatic disease (ileum).- Metastatic disease (appendix).- Metastatic disease (bronchi.- Metastatic disease with unknown primary tumour.
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Incidence;clinical presentation;diagnosis;prognosis;therapy