2019New England Journal of MedicineRequires access

Pheochromocytoma and Paraganglioma

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

Open publisher page 727 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.

About this research paper

What this paper is about

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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OpenAlex reports 727 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available 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.

Key concepts: Paraganglioma, Pheochromocytoma, Medicine, Pathology

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