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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Detalles Bibliográficos
Autores principales: Choo, Kuan Swen, Ngeow, Joanne Yuen Yie, Shaw, Tarryn, Tay, Donovan Yu-Kwang, Puar, Troy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Tumor Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552045/
http://dx.doi.org/10.1210/js.2019-SAT-317

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552045/
http://dx.doi.org/10.1210/js.2019-SAT-317

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