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Radionuclide Imaging of Chromaffin Cell Tumors

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Diagnostic and Therapeutic Nuclear Medicine for Neuroendocrine Tumors

Part of the book series: Contemporary Endocrinology ((COE))

Abstract

Pheochromocytomas (PHEOs) and extra-adrenal paragangliomas (PGLs) are neural crest-derived tumors associated with the sympathetic or parasympathetic nervous systems. Successful pheochromocytoma/paraganglioma management now requires an interdisciplinary team approach. Precise identification of clinical context and the patient’s genetic status enables a personalized use of genetic and biochemical tests carefully followed by the application of genotype- and biochemical-specific functional imaging modalities. Once these tumors are identified, their patient-specific management, termed personalized medicine, is applied to achieve the best treatment outcome. This chapter particularly emphasizes the current and emerging knowledge of imaging options for chromaffin tumors tailored to their unique localization, biochemical phenotype, genetic landscape, malignant predisposition, and, ultimately, metastasis.

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Taïeb, D., Pacak, K. (2017). Radionuclide Imaging of Chromaffin Cell Tumors. In: Pacak, K., Taïeb, D. (eds) Diagnostic and Therapeutic Nuclear Medicine for Neuroendocrine Tumors. Contemporary Endocrinology. Humana Press, Cham. https://doi.org/10.1007/978-3-319-46038-3_14

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