A Case of Asymptomatic Multiple Paragangliomas
Author:
Affiliation:
1. Department of Gastroenterological Surgery I, Hokkaido University Graduate School of Medicine
2. Department of Surgical Pathology, Hokkaido University Hospital
Publisher
Japan Surgical Association
Subject
General Engineering
Link
https://www.jstage.jst.go.jp/article/jjsa/77/7/77_1831/_pdf
Reference17 articles.
1. 1) Erickson D, Kudva YC, Ebersold MJ, et al : Benign paragangliomas : clinical presentation and treatment outcomes in 236 patients. J Clin Endocrinol Metab 2001 ; 86 : 5210-5216
2. 2) Barski D : Management and follow up of extra-adrenal phaeochromocytoma. Cent European J Urol 2014 ; 67 : 156-161
3. 3) Lefebvre M, Foulkes WD : Pheochromocytoma and paraganglioma syndromes : genetics and management update. Curr Oncol 2014 ; 21 : e8-e17
4. 5) Svajdler Mm, Bohus P, Závacký P, et al : Paraganglioma of the mesenterium : a case report. Cesk Patol 2007 ; 43 : 153-156
5. 6) Neumann HP : Phaeochromocytoma. Harrison's Principles of Internal Medicine, 17th ed., McGraw-Hill Medical, New York, London, 2008, p2269-2274
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