Abstract
Neuroendocrine tumors (NETs) arise from amine precursor uptake and decarboxylation (APUD) cells throughout the nervous and endocrine systems, which produce and secrete regulatory hormones. NETs commonly originate in: (1) argentaffin cells of the gut, resulting in carcinoid tumors, (2) endocrine cells in the pancreas, (3) calcitonin-producing thyroid cells, resulting in medullary thyroid carcinoma (MTC), and (4) parathyroid, adrenal, and pituitary glands. Although NETs are relatively rare and more indolent than other malignancies, occasionally they can be aggressive. Early diagnosis and accurate identification of primary tumors and metastases are necessary to appropriately treat patients before they develop complications from an aggressive disease. Imaging plays an important role in locating primary tumors, staging, and preoperative planning for resection of primary tumor and metastatic disease, and patient monitoring (follow-up). This chapter will focus on imaging modalities commonly used to diagnose and stage NETs with origins primarily in the abdomen, including gastrointestinal (GI) carcinoids, pancreatic islet-cell tumors, pheochromocytomas, and paragangliomas.
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Boonsirikamchai, P., Asran, M.K.A., Charnsangavej, C. (2011). Imaging of Neuroendocrine Tumors. In: Yao, J., Hoff, P., Hoff, A. (eds) Neuroendocrine Tumors. Current Clinical Oncology. Humana Press. https://doi.org/10.1007/978-1-60327-997-0_5
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