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SAT-317 The Importance of Accurate Genetic Diagnosis Highlighted in a Case of Recurrent Bilateral Pheochromocytomas

Background It is estimated that one-third of patients with pheochromocytomas and paragangliomas (PPGL) have germline mutations. This patient with bilateral pheochromocytomas was initially diagnosed with MEN2A syndrome, underwent prophylactic total thyroidectomy, only to be diagnosed with a different...

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Détails bibliographiques
Publié dans:J Endocr Soc
Auteurs principaux: Choo, Kuan Swen, Ngeow, Joanne Yuen Yie, Shaw, Tarryn, Tay, Donovan Yu-Kwang, Puar, Troy
Format: Artigo
Langue:Inglês
Publié: Endocrine Society 2019
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6552045/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SAT-317
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