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...

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Publicado en:Surg Case Rep
Autores principales: Okada, Ryo, Shimura, Tatsuo, Tsukida, Shigeyuki, Ando, Jin, Kofunato, Yasuhide, Momma, Tomoyuki, Yashima, Rei, Koyama, Yoshihisa, Suzuki, Shinichi, Takenoshita, Seiichi
Formato: Artigo
Lenguaje:Inglês
Publicado: Springer Berlin Heidelberg 2016
Materias:
Case Report
Acceso en línea: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
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