MON-321 Metastatic Melanoma with Unknown Primary Site in a Patient with Multiple Endocrine Neoplasia Type 1

Background: MEN1 is a rare hereditary tumor syndrome caused by germline inactivating mutations of the tumor suppressor gene MEN1 and is characterized by a predisposition to endocrine tumors primarily of parathyroid, enteropancreatic, and anterior pituitary origin, as well as nonendocrine neoplasms....

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Bibliographic Details
Published in:J Endocr Soc
Main Authors: Kamilaris, Crystal, Mandl, Adel, Simonds, William, Weinstein, Lee, Agarwal, Sunita, Blau, Jenny
Format: Artigo
Language:Inglês
Published: Endocrine Society 2019
Subjects:
Tumor Biology
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6550817/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-321
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