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...

Descripción completa

Detalles Bibliográficos
Autores principales: Okada, Ryo, Shimura, Tatsuo, Tsukida, Shigeyuki, Ando, Jin, Kofunato, Yasuhide, Momma, Tomoyuki, Yashima, Rei, Koyama, Yoshihisa, Suzuki, Shinichi, Takenoshita, Seiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005233/
https://www.ncbi.nlm.nih.gov/pubmed/27572829
http://dx.doi.org/10.1186/s40792-016-0214-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005233/
https://www.ncbi.nlm.nih.gov/pubmed/27572829
http://dx.doi.org/10.1186/s40792-016-0214-x

Ejemplares similares