SAT-223 Metastatic Pheochromocytoma in MEN2A: Clinical Features, Laboratory Data and Radiological Findings of a Rare Association - Case Report

Background: Multiple endocrine neoplasia type 2A (MEN2A) is an autosomal dominant syndrome caused by inactivating mutations in the RET proto-oncogene. It is characterized by medullary thyroid carcinoma (MTC), pheochromocytoma (PHEO) and hyperparathyroidism (HPTH). MTC is one of the initial manifesta...

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Detalles Bibliográficos
Publicado en:J Endocr Soc
Autores principales: d’Acampora, Ana Clara, Pilletti, Karine, Réus, Bruna da Silva, dos Santos, Debora Monteiro Alves, Marques, Emerson Leonildo, Ronsoni, Marcelo Fernando, Colombo, Giovani, Vieira, Daniella Serafin Couto, Farina Pasinato, Ana Paula Beltrame, Alencar, Guilherme Asmar
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2020
Materias:
Adrenal
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7207526/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.1469
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