Pheochromocytoma and paraganglioma

Hartmut P.H. Neumann; William F. Young; Charis Eng

doi:10.1056/NEJMra1806651

Pheochromocytoma and paraganglioma

Hartmut P.H. Neumann, William F. Young, Charis Eng

Endocrinology, Diabetes, Metabolism, and Nutrition

Research output: Contribution to journal › Review article › peer-review

83 Scopus citations

Abstract

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.

Original language	English (US)
Pages (from-to)	552-565
Number of pages	14
Journal	New England Journal of Medicine
Volume	381
Issue number	6
DOIs	https://doi.org/10.1056/NEJMra1806651
State	Published - Aug 8 2019

ASJC Scopus subject areas

General Medicine

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10.1056/NEJMra1806651

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title = "Pheochromocytoma and paraganglioma",

abstract = "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.",

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AB - 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.

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Pheochromocytoma and paraganglioma

Abstract

ASJC Scopus subject areas

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