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Pheochromocytoma: Recommendations for Clinical Practice from the First International Symposium on Pheochromocytoma - ISP2005 

Background:

Many options exist for diagnosis and management of the patient with pheochromocytoma, with practices varying among different centers and recommendations more often based on institutional experience than on evidence-based medicine. Progress on the latter front is limited by the rarity of the tumor and the subsequent fragmented nature of studies, most of which involve small numbers of patients or case reports.

Nevertheless, the forming of international consortia and multicenter studies to pool patient material, resources and experience is leading to increased progress. Improvements in diagnosis, localization, management and treatment of pheochromocytomas have also been fueled by leaps in our understanding of the genetics and biology of these tumors, coupled with advances in analytical chemistry, genomics, molecular biology, biotechnology and nuclear medicine. Ineffective treatments for malignant tumors, inadequate methods to distinguish malignant from benign disease, and lack of consensus on how to apply recent scientific and medical advances to improve diagnosis and patient management remain important unresolved problems.

An important feature of ISP2005 centered around several breakout sessions held to stimulate discussion on problem issues that could benefit from resolution in the form of recommendations, or where possible some form of consensus from leaders in the field. Under the guidance of impartial moderators, participants were asked to formulate recommendations that were subsequently discussed and agreed upon at a final general session of the Symposium where all attendees could be present.

The outcome of these breakout sessions, including recommendations that arose from discussions, has been published in several monographs as part of the Proceedings of the meeting. A condensed version of the material in those monographs is also being published in review form elsewhere:

Pacak, K. et al. Pheochromocytoma: recommendations for clinical practice from the first international symposium. Nature: Clinical Practice, Endocrinology & Metabolism "in press", 2006.

Those recommendations and related details are also presented here representing the combined efforts of PRESSOR members.

 
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