Abstract
Neuroendocrine tumors encompass a wide range of uncommon neoplasms derived from diverse tissues and from cells that are believed to have a common embryological origin from neural crest and closely related tissues [1–4] (Table 1.1). Among the features of these tissues, cells, and tumors are: the capacity to synthesize peptide neurotransmitter/hormones; biogenic amine precursor uptake and decarboxylation (hence the terms APUD and APUDomas); intracytoplasmic storage granules on electron microscopy and formalin induced fluorescence (FIF) [5–7]. Many also express cell surface receptors for somatostatin. Nuclear medicine has exploited biogenic amine uptake and cytoplasmic granule storage mechanisms for metaiodobenzylguanidine (MIBG) and related radiopharmaceuticals, and somatostatin receptors for radiolabeled somato-statin-analogs (e.g., [111In-DTPA]octreotide), for imaging tumors of neuroendocrine origin.
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Shapiro, B., Fig, L.M., Gross, M.D., Shulkin, B.L., Sisson, J.C. (1999). Neuroendocrine Tumors. In: Aktolun, C., Tauxe, W.N. (eds) Nuclear Oncology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-58643-9_1
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