Pheochromocytomas and Secreting Paragangliomas
Author Information
Author(s): Plouin Pierre-François, Gimenez-Roqueplo Anne-Paule
Primary Institution: Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris; Université René Descartes-Paris 5, France
Conclusion
Pheochromocytomas and secreting paragangliomas are rare tumors that can cause significant health issues due to catecholamine overproduction, and they require careful diagnosis and management.
Supporting Evidence
- The prevalence of these tumors is about 0.1% in patients with hypertension.
- Familial cases are diagnosed earlier and are more frequently bilateral and recurring than sporadic cases.
- The most specific diagnostic test is the determination of plasma or urinary metanephrines.
Takeaway
Some tumors in the body can make too much of certain chemicals that can make you feel sick. Doctors need to find and remove these tumors to help you feel better.
Methodology
The study reviews the epidemiology, diagnosis, and management of pheochromocytomas and secreting paragangliomas, including genetic factors and treatment options.
Digital Object Identifier (DOI)
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