• A N A van der Horst-Schrivers, M N Kerstens, and B H R Wolffenbuttel.
• Department of Endocrinology, University Medical Centre Groningen, University of Groningen, Groningen, the Netherlands. a.na.van.der.horst@int.umcg.nl
• Neth J Med. 2006 Sep 1;64(8):290-5.

AbstractPhaeochromocytoma is a rare catecholamine-secreting neuroendocrine tumour with a high cardiovascular morbidity and mortality if left untreated. Surgical resection is the only curative therapy. During surgery there is a high risk of massive release of catecholamines, which can result in potentially fatal hypertensive crises and cardiac arrhythmias. Administration of vasoactive drugs such as (non)selective alpha- and beta-antagonists and calcium channel blocking agents have reduced the operation risk. Guidelines for the preoperative medical management of the patient with a phaeochromocytoma are mainly based on retrospective studies and case reports. We reviewed the relevant literature on this subject. In addition, we compared the several preoperative treatment protocols of the eight university medical centres in the Netherlands.

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