Pheochromocytoma CT: Difference between revisions
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Revision as of 19:31, 1 August 2012
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Pheochromocytoma Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Pheochromocytoma CT On the Web |
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American Roentgen Ray Society Images of Pheochromocytoma CT |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
A pheochromocytoma (phaeochromocytoma outside of the US) is a neuroendocrine tumor of the medulla of the adrenal glands (originating in the chromaffin cells) or extra-adrenal chromaffin tissue which failed to involute after birth,[1] which secretes excessive amounts of catecholamines, usually epinephrine and norepinephrine. Extra-adrenal paragangliomas (often described as extra-adrenal pheochromocytomas) are closely related, though less common, tumors that originate in the ganglia of the sympathetic nervous system and are named based upon the primary anatomical site of origin.
Patient #1: Bladder pheochromocytoma
Patient #2
Patient #3
References
- ↑ Boulpaep, Emile L.; Boron, Walter F. (2003). Medical physiology: a cellular and molecular approach. Philadelphia: Saunders. p. 1065. ISBN 0-7216-3256-4.
de:Phäochromozytom it:Feocromocitoma he:פאוכרומוציטומה nl:Feochromocytoom sv:Feokromocytom