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Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2004-1077
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The Journal of Clinical Endocrinology & Metabolism Vol. 90, No. 1 563-569
Copyright © 2005 by The Endocrine Society


CLINICAL CASE SEMINAR

Hemorrhagic Pheochromocytoma Associated with Systemic Corticosteroid Therapy and Presenting as Myocardial Infarction with Severe Hypertension

Hilary Brown1, Philip A. Goldberg1, Jared G. Selter1, Henry S. Cabin, Norman J. Marieb, Robert Udelsman and John F. Setaro

Sections of Endocrine Surgery (H.B., R.U.), Endocrinology (P.A.G., N.J.M.), and Cardiovascular Medicine (J.G.S., H.S.C., J.F.S.), Yale University School of Medicine, New Haven, Connecticut 06520-8017

Address all correspondence and requests for reprints to: John F. Setaro, M.D., 333 Cedar Street, 3 FMP, P.O. Box 208017, New Haven, Connecticut 06520-8017. E-mail: john.setaro{at}yale.edu.

Pheochromocytomas classically present with paroxysms of hypertension and adrenergic symptoms including headaches, palpitations, tremor, and anxiety. However, these tumors can be clinically silent and occasionally present only when catecholamine release is up-regulated by exogenous stimuli. In addition, the clinical presentation of pheochromocytoma can mimic a number of more common medical conditions, including migraine headaches, cardiac arrhythmias, and myocardial infarction, making diagnosis difficult. In this report, we present the case of a young woman who, while receiving oral corticosteroid therapy for presumed migraine headaches, suffered a myocardial infarction and ultimately hemorrhaged into a previously undiagnosed pheochromocytoma. Our patient exhibited severe, labile hypertension after the administration of iv ß-blockade for presumed myocardial ischemia, raising our initial clinical suspicion for pheochromocytoma. In this paper we review some of the key clinical issues related to this complex case, including steroid-induced stimulation of catecholamine synthesis and release, the role of pheochromocytoma in myocardial ischemia and electrocardiographic changes, and the rare complication of tumor hemorrhage. We then briefly review the essential diagnostic and management strategies for this rare but potentially lethal tumor, with specific emphasis on pheochromocytoma-related cardiovascular emergencies and the surgical management of tumor hemorrhage.




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