Titlebook: Neuroendocrine Tumours; Diagnosis and Manage Suayib Yalcin,Kjell Öberg Book 2024Latest edition Springer Nature Switzerland AG 2024 Neuroend

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Neuroendocrine Neoplasms (NENs) in Complex Genetic Disorders,gastrointestinal, pancreatic, lung and thymic carcinoids are sporadic. However, some of the NENs may occur as part of multisystem autosomal dominant inherited genetic disorders, such as multiple endocrine neoplasia type 1 (MEN1) syndrome, von Hippel–Lindau (VHL) disease, neurofibromatosis type 1 (NF

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Neuroendocrine Tumors of the Lung,g carcinomas (SCLCs), depending on the appearance in light microscopy. Typical and atypical carcinoids are slow growing tumors, yet with malignant potential, while LCNEC and SCLC are highly malignant tumors with early development of metastases. Respiratory symptoms, such as cough, hemoptysis, and re

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Update of Neuroendocrine Tumors, Diagnosis, and Management,ll intestinal, colonic, rectal, and appendiceal tumors. In the SEER register, gastroenteropancreatic NETs constitute more than 60% of all NETs with the highest frequency being in the rectum (17.7%), small intestinal (17.3%), and colon (10.1%)..The genetic background of NETs is still not clearly unde

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Overview of Functioning Pancreatic Neuroendocrine Tumors (F-panNETs), associated with a clinical syndrome due to one or more hormones secreted by the tumor cells. Compared to the more common nonfunctioning F-panNETs, they are characterized by distinct clinical features that need to be taken in consideration for treatment decision-making. In this chapter, a comprehens

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Insulinoma,a comprehensive overview of the clinical and laboratory manifestations of insulinomas, their differential diagnosis, and available treatment options..Insulinomas can cause a wide range of clinical manifestations, including confusion, dizziness, blurred vision, sweating, palpitations, weakness, fatig

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