계명대학교 의학도서관 Repository

갈색세포종(증례보고)

Metadata Downloads
Author(s)
조원현박영관이상숙장은숙
Alternative Author(s)
Cho, Won HyunPark, Young KwanLee, Sang SookChang, Eun Sook
Publication Year
1988
Abstract
Pheochromocytoma is a tumor which produces catecholamine and its metabolites and are usually benign unilateral neoplasm of adrenal medulla in more than 80%. In rare cases, it may arise in an extraadrenal sites including perirenal fat, paraganglia, urinary bladder, chest and neck. In less than 1% of hypertension population, pheochromocytoma is a cause of hypertension and most of these cases are curative by surgery. The most common clinical finding is hypertension and it has three frequent symptoms of headache, palpitation and perspiration. The tumor can be diagnosed by urinary excretion of catecholamine and their metabolites such as vanillylmandelic acid and metanephrines. Other tumor, compeuterlized tomogram, 1131 MIBG scitigram, selective arteriogram and selective caval sampling for catecholamine are used. Authors experienced an extraadreanl pheochromocytoma in 71 years old male with intermittent hypertension and huge abdominal mass so reported the case and reviewed literature.
Alternative Title
Paraganglioma (a case report)
Department
Dept. of Surgery (외과학)
Dept. of Pathology (병리학)
Publisher
Keimyung University School of Medicine
Citation
Keimyung Medical Journal, Vol.7(1) : 172-177, 1988
Type
Article
URI
http://kumel.medlib.dsmc.or.kr/handle/2015.oak/14529
Authorize & License
  • AuthorizeOpen
Files in This Item:

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.