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Phaeochromocytoma and paraganglioma.

Authors :
Tarling JA
Kumar R
Ward LJ
Boot C
Wassif WS
Source :
Journal of clinical pathology [J Clin Pathol] 2024 Jul 18; Vol. 77 (8), pp. 507-516. Date of Electronic Publication: 2024 Jul 18.
Publication Year :
2024

Abstract

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.<br />Competing Interests: Competing interests: None declared.<br /> (© Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.)

Details

Language :
English
ISSN :
1472-4146
Volume :
77
Issue :
8
Database :
MEDLINE
Journal :
Journal of clinical pathology
Publication Type :
Academic Journal
Accession number :
38453430
Full Text :
https://doi.org/10.1136/jcp-2023-209234