Malignant and Metastatic Pheochromocytoma: Case Report and Review of the Literature

被引:6
|
作者
Johnson, Michael H. [1 ]
Cavallo, Jaime A. [1 ]
Figenshau, R. Sherburne [1 ]
机构
[1] Washington Univ, Sch Med, Dept Gen Surg, Div Urol, St Louis, MO 63130 USA
关键词
Pheochromocytoma; Neuroendocrine; Adrenal; Renal;
D O I
10.1016/j.eucr.2014.05.001
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Pheochromocytomas are rare neuroendocrine tumors. Although predominantly occurring in the adrenal glands, these tumors can present anywhere along the sympathetic chain. Indeed, classical teaching states that 10% of pheochromocytomas are extra-adrenal and 10% are malignant. We report a case of a 61-year-old female who underwent presumptive cytoreductive nephrectomy and adrenalectomy for renal carcinoma but was instead found to have malignant pheochromocytoma. Proper identification, surgical extirpation, and follow-up are imperative for treatment. We review the classic and current literature regarding management of this uncommon tumor. (C) 2014 The Authors. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:139 / 141
页数:3
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