1. Evaluation and Surgical Management of Multiple Endocrine Neoplasias.
- Author
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Frye CC, Brown TC, and Olson JA Jr
- Subjects
- Humans, Multiple Endocrine Neoplasia surgery, Multiple Endocrine Neoplasia diagnosis, Multiple Endocrine Neoplasia genetics
- Abstract
Multiple endocrine neoplasia (MEN) syndromes are rare autosomal dominant diseases that are associated with a mixture of both endocrine and non-endocrine tumors. Traditionally, there are 2 types of MEN that have unique clinical associations: MEN 1 (parathyroid hyperplasia, pancreatic neuroendocrine tumors, and pituitary tumors) and MEN 2 (medullary thyroid carcinoma and pheochromocytoma), which is further classified into MEN 2A (adds parathyroid adenomas) and 2B (adds ganglioneuromas and marfanoid habitus). Many of the endocrine tumors are resected surgically, and the pre, intra, and postoperative management strategies used must take into account the high recurrence rates asscioated with MEN tumors., Competing Interests: Disclosure C.C. Frye reports that he and his wife own equity in Neurocrine Biosciences and OpComm Solutions, Inc and that he serves as a Director for OpComm Solutions, Inc (neither of these companies are related to this project). The remaining authors report no disclosures., (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Published
- 2024
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