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

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...

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Main Authors: John Monge, MD, Daniel Homuth, DO, Loren Zuiderveld, MD
Format: Article
Language:English
Published: Elsevier 2019-04-01
Series:Radiology Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S1930043318305557
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spelling doaj-4f7ec6c5b4f24cc6bf68a8e6861df9912020-11-24T22:07:35ZengElsevierRadiology Case Reports1930-04332019-04-01144439443Multimodality appearance of multiple endocrine neoplasia type 1: A case reportJohn Monge, MD0Daniel Homuth, DO1Loren Zuiderveld, MD2Advocate Illinois Masonic Medical Center, 836 W Wellington Ave, Chicago, IL 60657, USACorresponding author.; Advocate Illinois Masonic Medical Center, 836 W Wellington Ave, Chicago, IL 60657, USAAdvocate Illinois Masonic Medical Center, 836 W Wellington Ave, Chicago, IL 60657, USAMultiple 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. Keywords: Multiple endocrine neoplasia type 1http://www.sciencedirect.com/science/article/pii/S1930043318305557
collection DOAJ
language English
format Article
sources DOAJ
author John Monge, MD
Daniel Homuth, DO
Loren Zuiderveld, MD
spellingShingle John Monge, MD
Daniel Homuth, DO
Loren Zuiderveld, MD
Multimodality appearance of multiple endocrine neoplasia type 1: A case report
Radiology Case Reports
author_facet John Monge, MD
Daniel Homuth, DO
Loren Zuiderveld, MD
author_sort John Monge, MD
title 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_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_sort multimodality appearance of multiple endocrine neoplasia type 1: a case report
publisher Elsevier
series Radiology Case Reports
issn 1930-0433
publishDate 2019-04-01
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. Keywords: Multiple endocrine neoplasia type 1
url http://www.sciencedirect.com/science/article/pii/S1930043318305557
work_keys_str_mv AT johnmongemd multimodalityappearanceofmultipleendocrineneoplasiatype1acasereport
AT danielhomuthdo multimodalityappearanceofmultipleendocrineneoplasiatype1acasereport
AT lorenzuiderveldmd multimodalityappearanceofmultipleendocrineneoplasiatype1acasereport
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