Concomitant existence of pheochromocytoma in a patient with multiple endocrine neoplasia type 1

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal-dominant inherited disorder that is classically characterized by the presence of neoplastic lesions of the parathyroid glands, the anterior pituitary gland, and the pancreas. However, MEN1 with concomitant pheochromocytoma is ext...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Surg Case Rep
Main Authors: Okada, Ryo, Shimura, Tatsuo, Tsukida, Shigeyuki, Ando, Jin, Kofunato, Yasuhide, Momma, Tomoyuki, Yashima, Rei, Koyama, Yoshihisa, Suzuki, Shinichi, Takenoshita, Seiichi
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2016
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5005233/
https://ncbi.nlm.nih.gov/pubmed/27572829
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40792-016-0214-x
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados