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- Title
It's not a mystery, it's in the history: Multidisciplinary management of multiple endocrine neoplasia type 1.
- Authors
Shirali, Aditya S.; Pieterman, Carolina R. C.; Lewis, Mark A.; Hyde, Samuel M.; Makawita, Shalini; Dasari, Arvind; Thosani, Nirav; Ikoma, Naruhiko; McCutcheon, Ian E.; Waguespack, Steven G.; Perrier, Nancy D.
- Abstract
Pituitary tumors and hyperplasia in multiple endocrine neoplasia type 1 syndrome (MEN1): a case-control study in a series of 77 patients versus 2509 non-MEN1 patients. Even if asymptomatic, the patient with MEN1 should undergo comprehensive screening for tumors that are part of the MEN1 spectrum: duodenopancreatic NETs (dpNETs), pituitary adenomas (PAs), thoracic NETs (bronchopulmonary and thymic), adrenal tumors, and gastric NETs. The patient (ML) was followed at the Mayo Clinic in Rochester, Minnesota, from 2009 to 2012, at The University of Texas MD Anderson Cancer Center from 2013 to 2016, and at Intermountain Healthcare of Utah from 2017 onward. Figure 4 outlines the basic considerations when managing a patient suspected to have MEN1.1,10,11,15,32,36,65Patient PerspectiveThe self-diagnosis of MEN1 was a seminal event in my personal and professional development.
- Subjects
ADRENAL tumors; PANCREATIC tumors; TUMORS; MEDICAL personnel; MAGNETIC resonance imaging; SYMPTOMS; SOMATOMEDIN C
- Publication
CA: A Cancer Journal for Clinicians, 2021, Vol 71, Issue 5, p369
- ISSN
0007-9235
- Publication type
Article
- DOI
10.3322/caac.21673