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

HONDA M; UESUGI K; YAMAZAKI H; DEZAWA A; MIZUGUCHI K; YAMAJI T; ISHIBASHI M

Art

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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Material：
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

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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