Abstract
Hypertensive crisis caused by pheochromocytoma/paraganglioma-related hypercatecholaminemia represents true endocrine emergency and associates with significant morbidity. Although rare, it is associated with potentially devastating complications and should be part of differential diagnosis in cases of treatment-resistant or paroxysmal hypertension, as well as hypertension of young patients. One also needs to remember that disease can be familial, can associate with multiple widely distributed tumors, as well as represent metastatic forms. Hypertensive crisis can be precipitated by numerous causes, including among others anesthesia, stress, exercise, and certain foods. While patients with known disease can be efficiently treated with aggressive regimen of α- and β-adrenergic or calcium-channel blockers and ultimately surgery, patients with unknown disease are the ones who develop acute severe hypertensive crisis during unrelated surgeries, manipulations in tumor areas, or physical/emotional stress. This calls for high degree of pheochromocytoma/paraganglioma awareness and understanding that only rapid and intensive treatment can be efficient in management of these patients.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Neumann HP, Vortmeyer A, Schmidt D, Werner M, Erlic Z, Cascon A, et al. Evidence of MEN-2 in the original description of classic pheochromocytoma. N Eng J Med. 2007;357:1311–5.
Pacak K, Chrousos GP, Koch CA, Lenders JW, Eisenhofer G. Pheochromocytoma: progress in diagnosis, therapy, and genetics. In: Margioris A, Chrousos GP, editors. Adrenal disorders, vol. 1. 1st ed. Totowa: Humana Press; 2001. p. 479–523.
Manger WM. The protean manifestations of pheochromocytoma. Horm Metab Res. 2009;41(09):658–63.
King KS, Prodanov T, Kantorovich V, Fojo T, Hewitt JK, Zacharin M, Wesley R, Lodish M, Raygada M, Gimenez-Roqueplo AP, McCormack S, Eisenhofer G, Milosevic D, Kebebew E, Stratakis CA, Pacak K. Metastatic pheochromocytoma/paraganglioma related to primary tumor development in childhood or adolescence: significant link to SDHB mutations. J Clin Oncol. 2011;29(31):4137–42.
Engleman K, Zelis R, Waldmann T, et al. Mechanism of orthostatic hypotension in pheochromocytoma. Circulation. 1968;38 Suppl 6:71–2.
Manger W, Gifford RW. The clinical and experimental pheochromocytoma. 2nd ed. Malden (MA): Blackwell Science; 1996.
Brouwers FM, Eisenhofer G, Lenders JW, Pacak K. Emergencies caused by pheochromocytoma, neuroblastoma, or ganglioneuroma. Endocrinol Metab Clin North Am. 2006;35(4):699–724.
Prejbisz A, Lenders JW, Eisenhofer G, Januszewicz A. Cardiovascular manifestations of phaeochromocytoma. J Hypertens. 2011;29(11):2049–60.
Widimský Jr J. Recent advances in the diagnosis and treatment of pheochromocytoma. Kidney Blood Press Res. 2006;29(5):321–6.
Manger WM. An overview of pheochromocytoma: history, current concepts, vagaries, and diagnostic challenges. Ann N Y Acad Sci. 2006;1073:1–20.
Eisenhofer G, Rivers G, Rosas AL, Quezado Z, Manger WM, Pacak K. Adverse drug reactions in patients with phaeochromocytoma: incidence, prevention and management. Drug Saf. 2007;30(11):1031–62.
Rosas AL, Kasperlik-Zaluska AA, Papierska L, Bass BL, Pacak K, Eisenhofer G. Pheochromocytoma crisis induced by glucocorticoids: a report of four cases and review of the literature. Eur J Endocrinol. 2008;158(3):423–9.
Eisenhofer G, Goldstein DS, Sullivan P, et al. Biochemical and clinical manifestations of dopamine-producing paragangliomas: utility of plasma methoxytyramine. J Clin Endocrinol Metab. 2005;90(4):2068–75.
Petrak O, Strauch B, Zelinka T, et al. Factors influencing arterial stiffness in pheochromocytoma and effect of adrenalectomy. Hypertens Res. 2010;33(5):454–9.
Hill FS, Jander HP, Murad T, et al. The coexistence of renal artery stenosis and pheochromocytoma. Ann Surg. 1983;197(4):484–90.
Salehi A, Legome EL, Eichhorn K, et al. Pheochromocytoma and bowel ischemia. J Emerg Med. 1996;15(1):35–8.
Sawaki D, Otani Y, Sekita G, Kobayakawa N, Fukushima K, Takeuchi H, Aoyagi T. Pheochromocytoma complicated with refractory paralytic ileus dramatically improved with intravenous administration of alpha-adrenergic receptor antagonist, phentolamine. J Clin Gastroenterol. 2003;37(2):194.
Schenker JG, Chowers I. Pheochromocytoma and pregnancy. Review of 89 cases. Obstet Gynecol Surv. 1971;26(11):739–47.
Lenders JW, Pacak K, Walther MM, Linehan WM, Mannelli M, Friberg P, Keiser HR, Goldstein DS, Eisenhofer G. Biochemical diagnosis of pheochromocytoma: which test is best? JAMA. 2002;287(11):1427–34.
Pacak K. Preoperative management of the pheochromocytoma patient. J Clin Endocrinol Metab. 2007;92(11):4069–79.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2014 Springer Science+Business Media New York
About this chapter
Cite this chapter
Kantorovich, V., Pacak, K. (2014). Pheochromocytoma Hypertensive Crisis. In: Loriaux, L. (eds) Endocrine Emergencies. Contemporary Endocrinology, vol 74. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-697-9_14
Download citation
DOI: https://doi.org/10.1007/978-1-62703-697-9_14
Published:
Publisher Name: Humana Press, Totowa, NJ
Print ISBN: 978-1-62703-696-2
Online ISBN: 978-1-62703-697-9
eBook Packages: MedicineMedicine (R0)