Pheochromocytoma and Paraganglioma Diagnosis, Genetics, and Treatment

被引：61
作者：
Kiernan, Colleen M. [1 ]
Solorzano, Carmen C. [1 ]
机构：
[1] Vanderbilt Univ, Med Ctr, Div Surg Oncol & Endocrine Surg, Nashville, TN 37232 USA
来源：
SURGICAL ONCOLOGY CLINICS OF NORTH AMERICA | 2016年 / 25卷 / 01期
关键词：
Neuroendocrine tumor; Pheochromocytoma; Paraganglioma; Biochemical evaluation; Genetics; Imaging; Perioperative management; Surgery; VONHIPPEL-LINDAU-DISEASE; NEUROENDOCRINE TUMORS PHEOCHROMOCYTOMA; POSITRON-EMISSION-TOMOGRAPHY; ENDOCRINE NEOPLASIA TYPE-2; MEDULLARY-THYROID-CANCER; BIOCHEMICAL-DIAGNOSIS; LAPAROSCOPIC ADRENALECTOMY; RISK-FACTORS; LOCALIZING PHEOCHROMOCYTOMAS; MALIGNANT PHEOCHROMOCYTOMAS;
D O I：
10.1016/j.soc.2015.08.006
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
This article highlights the epidemiology and pathophysiology of pheochromocytomas and paragangliomas. The current management of pheochromocytoma and paragangliomas, including utilization and interpretation of biochemical testing, preoperative imaging, and genetic screening are discussed. Furthermore, perioperative surgical management, outcomes, and recommended follow-up are reviewed.
引用
收藏
页码：119 / +
页数：21
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