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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Dades bibliogràfiques
Publicat a:J Endocr Soc
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2020
Matèries:
Adrenal
Accés en línia: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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