Abstract
Paragangliomas are neuroendocrine neoplasms that arise from chief cells in extra-adrenal paraganglia of the peripheral nervous system. While previous chapters have expanded upon historical, diagnostic, and management issues pertaining to paragangliomas, this chapter will discuss the management and prognosis regarding multicentric paragangliomas, malignant tumors, catecholamine-secreting paragangliomas, high-risk anesthetic patients, and future directions. Due to the paucity of literature on these particular topics, studies analyzing other head and neck paragangliomas, as well as non-head and neck paragangliomas and pheochromocytomas, are reviewed when relevant to highlight special considerations in management.
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Hunter, J.B. (2018). Special Considerations in Management of Jugular Paraganglioma. In: Wanna, G., Carlson, M., Netterville, J. (eds) Contemporary Management of Jugular Paraganglioma. Springer, Cham. https://doi.org/10.1007/978-3-319-60955-3_16
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DOI: https://doi.org/10.1007/978-3-319-60955-3_16
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