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KMID : 0371319840260010135
Journal of the Korean Surgical Society
1984 Volume.26 No. 1 p.135 ~ p.140
Pheochromocytoma
¼­±¤Áø/Seo, Kwangjin
À±¿µ¸ð/¹®Ã¶¼º/¼ÕÁ¾ÇÏ/Yoon, Youngmo/Moon, Chulsung/Son, Jongha
Abstract
Of the surgically correctable causes of hypertension, none has a more variable clinical presentation or a more volatile natural history than pheochromocytoma, functionally active chromaffin tumors which may be located in the adrenal medulla or other sites where sympathetic ganglia or chromaffin tissue are known to exist. Although the tumor is rare, several large series of patients with pheochromocytoma have been reported, and there is general agreement regarding the methods of diagnosis, tumor location, preoperative preparations and operative management of these patients.
We were experienced in successful management of a patient with pheochromocytoma by surgical intervention. With particular interest in unique characteristics of this tumor, we report our experience with review of literatures.
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