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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Endocr Soc
Autors principals: Roszko, Kelly Lauter, Blouch, Erica, Blake, Michael, Powers, James F., Tischler, Arthur S., Hodin, Richard, Sadow, Peter, Lawson, Elizabeth A.
Format: Artigo
Idioma:Inglês
Publicat: Endocrine Society 2017
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5686672/
https://ncbi.nlm.nih.gov/pubmed/29264463
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2017-00135
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars