Pheochromocytoma pathophysiology: Difference between revisions
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Revision as of 14:57, 11 September 2012
Pheochromocytoma Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Pheochromocytoma pathophysiology On the Web |
American Roentgen Ray Society Images of Pheochromocytoma pathophysiology |
Risk calculators and risk factors for Pheochromocytoma pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Pathophysiology
Traditionally it is known as the "10% tumor":
- bilateral disease is present in approximately 10% of patients
- approximately 10% of tumours are malignant
- approximately 10% are located in chromaffin tissue outside of the adrenal gland
- Approximately 10% arise in childhood
- Approximately 10% are familial
- Approximately 10% recur after being resected
- Approximately 10% patients do not have hypertension (Campbell's Urology)
Images
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Micrograph of pheochromocytoma.
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Micrograph of pheochromocytoma.
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Micrograph of pheochromocytoma.
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Bilateral pheochromocytoma in MEN2. Gross image.
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Pheochromocytoma. CT abdomen.
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Pheochromocytoma. CT abdomen.