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Phaeochromocytoma and paraganglioma.

Julie Ann TarlingRajeev KumarLouise J WardChristopher BootW S Wassif
Published in: Journal of clinical pathology (2024)
Phaeochromocytomas and paragangliomas are rare catecholamine-producing neuroendocrine tumours which can potentially cause catastrophic crises with high morbidity and mortality. This best practice article considers the causes and presentation of such tumours, screening and diagnostic tests, management of these patients and consideration of family members at risk.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • newly diagnosed
  • chronic kidney disease
  • primary care
  • healthcare
  • prognostic factors