Abstract
Neuroendocrine tumors (NET) include pheochromocytoma, neuroblastoma, carcinoid, paraganglioma, chemodectoma, medullary thyroid carcinoma, islet cell tumors, gastrinoma, small cell lung cancer, melanoma, and Merkel cell tumor. NET vary considerably in their clinical presentation, location, and histology but share a common embryonic tissue origin, i.e., the neural crest. In addition, all of these tumors express several unique characteristics that may be exploited in the targeting of radiopharmaceuticals for diagnostic as well as therapeutic purposes [1]. The specific targeting of NET may be achieved via the metabolic route (meta-iodo-benzylguanidine, MIBG), through receptor binding (peptides), or immunologically (antibodies).
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Hoefnagel, C.A. (2010). Tumors of the Adrenergic System: Imaging and Therapy. In: Hodler, J., Zollikofer, C.L., Von Schulthess, G.K. (eds) Diseases of the Abdomen and Pelvis 2010–2013. Springer, Milano. https://doi.org/10.1007/978-88-470-1637-8_31
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DOI: https://doi.org/10.1007/978-88-470-1637-8_31
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