Abstract
Pheochromocytomas are catecholamine-secreting tumors located in the adrenal gland. Patients may present with incidentally found adrenal nodules but commonly have symptoms related to catecholamine excess including paroxysmal hypertension, tremors, palpitations, and diaphoresis. Biochemical evaluation should include serum metanephrines with confirmatory testing with urinary catecholamines, including dopamine and creatinine for adequacy of sample. Cross-sectional imaging should be performed with and without intravenous (IV) contrast for localization. Pheochromocytomas typically show marked enhancement and are greater than 3 cm. Biopsy of the adrenal gland should never be performed. Surgical management with laparoscopic adrenalectomy unless the tumor is greater than 6 cm or has concerning imaging features suggestive of malignancy. Preoperative alpha blockade should be performed until the patient develops orthostatic hypotension, at which point beta blockade should be added to counteract rebound tachycardia.
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References
Assadiour Y, Sadowski SM, Alimchandani M, Quezado M, Steinberg SM, Nilubol N, Patel D, Prodanov T, Pacak K, Kebebew E. SDHB mutation status and tumor size but not grade are important predictors of clinical outcome in pheochromocytoma and abdominal paraganglioma. Surgery. 2017;161:230–9.
Melmed S, Polonsky KS, Larsen PR, Kronenberg HM. Chapter 16 endocrine hypertension. In: Williams textbook of endocrinology. 13th ed. Philadelphia: Elsevier; 2016. p. 566–88.
Van Berkel A, Rao JU, Kusters B, et al. Correlation between in vivo 18F-FDG PET and immunohistochemical markers of glucose uptake and metabolism in pheochromocytoma and paraganglioma. J Nucl Med. 2014;55:1253–9.
Lenders JWM, Duh Q-Y, Eisenhofer G, Giminez-Roqueplo A-P, Grebe SKG, Murad MH, Naruse M, Pacak K, Young WF Jr. Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2014;99(6):1915–42.
Suggested Reading
Clark OH, Duh Q-Y, Gosnell JE, Shen W. Textbook of endocrine surgery. 3rd ed. New Delhi: Jaypee Brothers Medical Publishers; 2014.
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Ritter, H.E., James, B.C. (2019). Management of Pheochromocytoma. In: Docimo Jr., S., Pauli, E. (eds) Clinical Algorithms in General Surgery . Springer, Cham. https://doi.org/10.1007/978-3-319-98497-1_113
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DOI: https://doi.org/10.1007/978-3-319-98497-1_113
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