Case Report of a Prolactinoma in a Patient With a Novel MAX Mutation and Bilateral Pheochromocytomas

Pheochromocytomas are neuroendocrine tumors that can arise sporadically or be inherited as a familial disease, and they may occur in isolation or as part of a multitumor syndrome. Familial disease typically presents in younger patients with a higher risk of multifocality. Recently, the tumor suppres...

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Detalles Bibliográficos
Autores principales: Roszko, Kelly Lauter, Blouch, Erica, Blake, Michael, Powers, James F., Tischler, Arthur S., Hodin, Richard, Sadow, Peter, Lawson, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686672/
https://www.ncbi.nlm.nih.gov/pubmed/29264463
http://dx.doi.org/10.1210/js.2017-00135

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686672/
https://www.ncbi.nlm.nih.gov/pubmed/29264463
http://dx.doi.org/10.1210/js.2017-00135

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