| Literature DB >> 31243023 |
WingYee Wan1, Bichle Nguyen1, Sky Graybill2, Jonathan Kim1.
Abstract
Compared with the general population, rates of pheochromocytoma are higher in neurofibromatosis type 1 (NF1) patients. However, pheochromocytoma testing is often plagued by false positive results. Here we present a patient with NF1, elevated urinary metanephrine levels, and an indeterminate adrenal nodule. Clonidine suppression testing aided diagnosis and led to definitive surgical treatment that confirmed a pheochromocytoma. Pheochromocytoma screening and clonidine suppression testing can both aid in the evaluation for catecholamine-secreting tumours. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: adrenal disorders; neuro genetics
Mesh:
Substances:
Year: 2019 PMID: 31243023 PMCID: PMC6605898 DOI: 10.1136/bcr-2018-228263
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X