Screening for Hereditary Pheochromocytoma in a Patient with Neurofibromatosis Type 1: A Case Report

Pheochromocytoma (PHEO) is a rare tumour that arises from adreno-medullary chromaffin cells and secretes catecholamines. These hormones are also secreted by paragangliomas, which derive from extra-adrenal cells of the sympathetic paravertebral ganglia. At least one-third of PHEOs are familial. Neuro...

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Salvato in:
Dettagli Bibliografici
Pubblicato in:touchREV Endocrinol
Autori principali: Ferreira Barros, Inês Isabel, Manso, Fernando, Caldas e Silva, Ana Isabel, Silva Lopes Pereira, Maria Ramires
Natura: Artigo
Lingua:Inglês
Pubblicazione: Touch Medical Media 2021
Soggetti:
Endocrine Oncology
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC8320010/
https://ncbi.nlm.nih.gov/pubmed/35118451
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.17925/EE.2021.17.1.79
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