1. Multiple Endocrine Neoplasia Syndromes: A Comprehensive Imaging Review.
- Author
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Grajo JR, Paspulati RM, Sahani DV, and Kambadakone A
- Subjects
- Diagnosis, Differential, Evidence-Based Medicine, Genetic Predisposition to Disease epidemiology, Genetic Predisposition to Disease genetics, Genetic Testing methods, Humans, Multiple Endocrine Neoplasia epidemiology, Prevalence, Risk Factors, Diagnostic Imaging methods, Multiple Endocrine Neoplasia diagnostic imaging, Multiple Endocrine Neoplasia genetics
- Abstract
MEN1, MEN2, and MEN4 comprise a series of familial disorders involving the simultaneous occurrence of tumors in more than one endocrine organ, collectively known as multiple endocrine neoplasia. Patients with this family of disorders develop tumors of the parathyroid gland, pancreas, pituitary gland, adrenal gland, and thyroid gland, along with miscellaneous neuroendocrine tumors of the respiratory and gastrointestinal tracts. Although some patients undergo early prophylactic surgical management, particularly in the setting of familial medullary thyroid carcinoma, many develop tumors later in life. These tumors are often discovered at imaging for screening purposes. Recognition of the imaging features of the known tumors is important for appropriate patient management., (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Published
- 2016
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