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J-GLOBAL ID:200902110701180803   Reference number:00A0977790

Malignant Pheochromocytoma Lacking Clinical Features of Catecholamine Excess Until the Late Stage.

末期までカテコールアミン過剰の臨床像がみられなかった悪性褐色細胞腫
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Volume: 39  Issue: 10  Page: 820-825  Publication year: Oct. 2000 
JST Material Number: Z0157B  ISSN: 0918-2918  Document type: Article
Article type: 短報  Country of issue: Japan (JPN)  Language: ENGLISH (EN)
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Tumors(=neoplasms)of nervous system 
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Reference (23):
  • 1) Mahoney EM, Harrison JH. Malignant pheochromocytoma: clinical course and treatment. J Urol 118: 225-229, 1977.
  • 2) Modlin IM, Farndon JR, Shepherd A, et al. Phaeochromocytomas in 72 patients: clinical and diagnostic features, treatment and long-term results. Br J Surg 66: 456-465, 1979.
  • 3) Scott HW Jr, Reynolds V, Green N, et al. Clinical experience with malignant pheochromocytomas. Surg Gynecol Obstet 154: 801-818, 1982.
  • 4) Takeda R, Yasuhara S, Miyamori I, Sato T, Miura Y. Phaeochromocytoma in Japan: analysis of 493 cases during 1973-1982. J Hypertens 4 (suppl 5): S397-S399, 1986.
  • 5) Schlumberger M, Gicquel C, Lumbroso J, et al. Malignant pheochromocytoma: clinical, biological, histologic and therapeutic data in a series of 20 patients with distant metastases. J Endocrinol Invest 15: 631-642, 1992.
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