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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Dettagli Bibliografici
Pubblicato in:Surg Case Rep
Autori principali: Okada, Ryo, Shimura, Tatsuo, Tsukida, Shigeyuki, Ando, Jin, Kofunato, Yasuhide, Momma, Tomoyuki, Yashima, Rei, Koyama, Yoshihisa, Suzuki, Shinichi, Takenoshita, Seiichi
Natura: Artigo
Lingua:Inglês
Pubblicazione: Springer Berlin Heidelberg 2016
Soggetti:
Case Report
Accesso online: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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