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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Cite This Study

Neumann et al. (Wed,) studied this question.

synapsesocial.com/papers/69fbe82fd8d80d4422b86602 https://doi.org/https://doi.org/10.1056/nejmra1806651

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Pheochromocytoma and Paraganglioma | Synapse

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Hormone‐secreting adrenal tumours cause severe hypertension and high rates of poor pregnancy outcome; a <scp>UK</scp> Obstetric Surveillance System study with case control comparisons2017 · 25 citations
2Von Hippel-Lindau disease in a Newfoundland kindred.

1986 · 76 citations

3Pheochromocytoma: The Expanding Genetic Differential Diagnosis2003 · 252 citations

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5Biochemical Diagnosis and Localization of Pheochromocytoma2006 · 127 citations