Abstract
In this chapter, we review the surgical and pharmacological management of hypersecretory endocrine disorders, including hyperaldosteronism, hyperparathyroidism, hyperandrogenism, pancreatic endocrine tumors, and hypercortisolism. Adrenalectomy is recommended for unilateral aldosterone producing adenomas, and mineralocorticoid receptor antagonists are used for those who cannot undergo surgery or have bilateral adenomas. Hyperparathyroidism is managed with surgery or medications, depending on the type of hyperparathyroidism and patient comorbidities. The treatment for hyperandrogenism depends on the underlying cause. Medical therapy is available for most causes of hyperandrogenism, but surgery is recommended for adrenal and ovarian tumors. Pancreatic endocrine tumors are surgically excised, but medical agents are available when needed. Hypercortisolism in Cushing’s syndrome is treated surgically, but medical therapy is available when surgery is not possible or unsuccessful. In this chapter, we also discuss the nuclear medicine options available for these disorders.
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References
Funder JW, Carey RM, Mantero F, Murad MH, Reincke M, Shibata H, et al. The management of primary aldosteronism: case detection, diagnosis, and treatment: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metabol. 2016;101(5):1889–916.
Bilezikian JP, Brandi ML, Eastell R, Silverberg SJ, Udelsman R, Marcocci C, et al. Guidelines for the management of asymptomatic primary hyperparathyroidism: summary statement from the fourth international workshop. J Clin Endocrinol Metabol. 2014;99(10):3561–9.
Marcocci C, Bollerslev J, Khan AA, Shoback DM. Medical management of primary hyperparathyroidism: proceedings of the fourth international workshop on the management of asymptomatic primary hyperparathyroidism. J Clin Endocrinol Metabol. 2014;99(10):3607–18.
Ketteler M, Block GA, Evenepoel P, Fukagawa M, Herzog CA, McCann L, et al. Executive summary of the 2017 KDIGO Chronic Kidney Disease–Mineral and Bone Disorder (CKD-MBD) guideline update: what’s changed and why it matters. Kidney Int. 2017;92(1):26–36.
Mettler F, Guiberteau M. Thyroid, parathyroid, and salivary glands. Essentials of nuclear medicine and molecular imaging. Elsevier; 2019. p. 85–115.
Ziessman H. Endocrine system. In: Nuclear medicine: the requisites. 4th ed. Philadelphia: Elsevier Mosby; 2015. p. 66–97.
Legro RS, Arslanian SA, Ehrmann DA, Hoeger KM, Murad MH, Pasquali R, et al. Diagnosis and treatment of polycystic ovary syndrome: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2013;98(12):4565–92.
Martin KA, Anderson RR, Chang RJ, Ehrmann DA, Lobo RA, Murad MH, et al. Evaluation and treatment of hirsutism in premenopausal women: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2018;103(4):1233–57.
Kulke MH, Anthony LB, Bushnell DL, de Herder WW, Goldsmith SJ, Klimstra DS, et al. NANETS treatment guidelines: well-differentiated neuroendocrine tumors of the stomach and pancreas. Pancreas. 2010;39(6):735–52.
Kunz PL, Reidy-Lagunes D, Anthony LB, Bertino EM, Brendtro K, Chan JA, et al. Consensus guidelines for the management and treatment of neuroendocrine tumors. Pancreas. 2013;42(4):557–77.
Mettler F, Guiberteau M. Non-PET neoplasm imaging and radionuclide therapy. Essentials of nuclear medicine and molecular imaging. Elsevier; 2019. p. 315–27.
Young K, Iyer R, Morganstein D, Chau I, Cunningham D, Starling N. Pancreatic neuroendocrine tumors: a review. Future Oncol. 2015;11(5):853–64.
Wang R, Zheng-Pywell R, Chen HA, Bibb JA, Chen H, Rose JB. Management of gastrointestinal neuroendocrine tumors. Clin Med Insights Endocrinol Diabetes. 2019;12:1179551419884058.
Nieman LK, Biller BMK, Findling JW, Murad MH, Newell-Price J, Savage MO, et al. Treatment of Cushing’s syndrome: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metabol. 2015;100(8):2807–31.
Varlamov E, Hinojosa-Amaya JM, Stack M, Fleseriu M. Diagnostic utility of Gallium-68-somatostatin receptor PET/CT in ectopic ACTH-secreting tumors: a systematic literature review and single-center clinical experience. Pituitary. 2019;22(5):445–55.
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Soliman, D., Qamar, A., Oldan, J.D. (2022). Medical Treatment of Hypersecretory Endocrine Disorders. In: Yu, H., Burke, C.T., Commander, C.W. (eds) Diagnosis and Management of Endocrine Disorders in Interventional Radiology. Springer, Cham. https://doi.org/10.1007/978-3-030-87189-5_11
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DOI: https://doi.org/10.1007/978-3-030-87189-5_11
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