Adrenal disease

Differences in Clinical Presentation Between Pheochromocytomas and Paragangliomas

Clin Endocrinol (Oxf)Published Retrospective cohort study

Authors' conclusion

Pheochromocytomas and paragangliomas exhibit some notable differences in symptoms and hormone profiles but generally share many features. These distinctions are, however, insufficient for clinicians to differentiate the two tumours based solely on clinical presentation or biochemical data.

Study context

Population
Patients with PPGLs treated at a major tertiary centre, 2005–2024196 with symptom data
Participants
201 patients
Exposure
Pheochromocytoma vs paraganglioma
Outcome
Differences in clinical presentation between pheochromocytomas and paragangliomas
Methodological detailssingle tertiary centre
  • Single tertiary centre

Main finding

As reported in the abstract

Clinical presentation

Paragangliomas producing increased epinephrine

25.0%

Classic triad (palpitations, sweating, headaches), all patients; similar between groups

12%

Hypertension, all patients; similar between groups

82%

Observational data: associations, not effects.

Original publication

Differences in Clinical Presentation Between Pheochromocytomas and Paragangliomas. Clin Endocrinol (Oxf). Published 10 July 2025. doi:10.1111/cen.70002

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