Pheochromocytoma and Paraganglioma

被引：344

作者：

Neumann, Hartmut P. H. ^{[1
]}

Young, William F., Jr. ^{[2
]}

Eng, Charis ^{[3
,4
]}

机构：

[1] Univ Freiburg, Albert Ludwigs Univ, Fac Med, Med Ctr,Sect Prevent Med, Freiburg, Germany

[2] Mayo Clin, Dept Internal Med, Div Endocrinol Diabet Metab & Nutr, Rochester, MN USA

[3] Cleveland Clin, Lerner Res Inst, Genom Med Inst, Cleveland, OH USA

[4] Cleveland Clin, Taussig Canc Inst, Cleveland, OH USA

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 2019年 / 381卷 / 06期

基金：

欧盟地平线“2020”;

关键词：

ENDOCRINE NEOPLASIA TYPE-2; ADRENAL-SPARING SURGERY; RENAL-CELL CARCINOMA; GERM-LINE MUTATIONS; SUCCINATE-DEHYDROGENASE; RETROPERITONEAL PARAGANGLIOMAS; MALIGNANT PHEOCHROMOCYTOMAS; LAPAROSCOPIC ADRENALECTOMY; FAMILIAL PHEOCHROMOCYTOMA; HIF2A MUTATIONS;

D O I：

10.1056/NEJMra1806651

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Pheochromocytoma and paraganglioma are related tumors that differ mainly in location; pheochromocytomas are adrenal, and paragangliomas can be anywhere else. The symptoms are protean and common, but the tumors are rare. The diagnosis may signify an underlying genetic syndrome.

引用

页码：552 / 565

页数：14

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