Phaeochromocytoma and paraganglioma.

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. © Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Citation

Julie Ann Tarling, Rajeev Kumar, Louise J Ward, Christopher Boot, W S Wassif. Phaeochromocytoma and paraganglioma. Journal of clinical pathology. 2024 Jul 18;77(8):507-516

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PMID: 38453430

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