Multimodality appearance of multiple endocrine neoplasia type 1: A case report

Multiple endocrine neoplasia type 1 is a rare autosomal dominant disorder classically characterized by a predisposition to tumors of the parathyroid glands, anterior pituitary, and enteropancreatic endocrine cells. We present the clinical details of a patient with diarrhea, nephrolithiasis, erectile...

Descripción completa

Detalles Bibliográficos
Autores principales: Monge, John, Homuth, Daniel, Zuiderveld, Loren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Multisystem
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352705/
https://www.ncbi.nlm.nih.gov/pubmed/30728878
http://dx.doi.org/10.1016/j.radcr.2019.01.007
_version_ 1783390901176893440
author Monge, John
Homuth, Daniel
Zuiderveld, Loren
author_facet Monge, John
Homuth, Daniel
Zuiderveld, Loren
author_sort Monge, John
collection PubMed
description Multiple endocrine neoplasia type 1 is a rare autosomal dominant disorder classically characterized by a predisposition to tumors of the parathyroid glands, anterior pituitary, and enteropancreatic endocrine cells. We present the clinical details of a patient with diarrhea, nephrolithiasis, erectile dysfunction, and new onset abdominal pain, as well as a discussion of the etiology, pathophysiology, and classical imaging findings of this condition.
format Online
Article
Text
id pubmed-6352705
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-63527052019-02-06 Multimodality appearance of multiple endocrine neoplasia type 1: A case report Monge, John Homuth, Daniel Zuiderveld, Loren Radiol Case Rep Multisystem Multiple endocrine neoplasia type 1 is a rare autosomal dominant disorder classically characterized by a predisposition to tumors of the parathyroid glands, anterior pituitary, and enteropancreatic endocrine cells. We present the clinical details of a patient with diarrhea, nephrolithiasis, erectile dysfunction, and new onset abdominal pain, as well as a discussion of the etiology, pathophysiology, and classical imaging findings of this condition. Elsevier 2019-01-23 /pmc/articles/PMC6352705/ /pubmed/30728878 http://dx.doi.org/10.1016/j.radcr.2019.01.007 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Multisystem
Monge, John
Homuth, Daniel
Zuiderveld, Loren
Multimodality appearance of multiple endocrine neoplasia type 1: A case report
title Multimodality appearance of multiple endocrine neoplasia type 1: A case report
title_full Multimodality appearance of multiple endocrine neoplasia type 1: A case report
title_fullStr Multimodality appearance of multiple endocrine neoplasia type 1: A case report
title_full_unstemmed Multimodality appearance of multiple endocrine neoplasia type 1: A case report
title_short Multimodality appearance of multiple endocrine neoplasia type 1: A case report
title_sort multimodality appearance of multiple endocrine neoplasia type 1: a case report
topic Multisystem
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352705/
https://www.ncbi.nlm.nih.gov/pubmed/30728878
http://dx.doi.org/10.1016/j.radcr.2019.01.007
work_keys_str_mv AT mongejohn multimodalityappearanceofmultipleendocrineneoplasiatype1acasereport
AT homuthdaniel multimodalityappearanceofmultipleendocrineneoplasiatype1acasereport
AT zuiderveldloren multimodalityappearanceofmultipleendocrineneoplasiatype1acasereport

Ejemplares similares