Pheochromocytoma surgery: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Pheochromocytoma}} | {{Pheochromocytoma}} | ||
{{CMG}} {{AE}} {{AAM}} | {{CMG}}; {{AE}} {{AAM}} | ||
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==Overview== | ==Overview== | ||
Surgery is the mainstay of treatment for pheochromocytoma. | Surgery is the mainstay of treatment for pheochromocytoma. | ||
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==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Endocrinology]] | [[Category:Endocrinology]] | ||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} |
Revision as of 20:14, 25 July 2016
Pheochromocytoma Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Pheochromocytoma surgery On the Web |
American Roentgen Ray Society Images of Pheochromocytoma surgery |
Risk calculators and risk factors for Pheochromocytoma surgery |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]
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Overview
Surgery is the mainstay of treatment for pheochromocytoma.
Surgery
- Surgical resection is the treatment of choice for benign localized tumor.
- Given the complexity of perioperative management, and the potential for catastrophic intra and postoperative complications, such surgery should be performed only at centers experienced in the area.
- It may also be nescessary to perform a complete surgical resection of the affected adrenal gland(s).