Multiple endocrine neoplasia: an update

Internal Medicine Journal
Jane E McDonnellBruce G Robinson

Abstract

The multiple endocrine neoplasia (MEN) syndromes include MEN1, MEN2 (formerly MEN2A), MEN3 (formerly MEN2B) and the recently identified MEN4. Clinical presentations are varied and often relate to the overproduction of specific hormones. Understanding the genetics of each syndrome assists in determining screening timelines. Treatments for each manifestation are dependent on location, risk of recurrence or malignancy, hormone excess and surgical morbidity. Multidisciplinary management should include geneticists, genetic counsellors, endocrinologists and endocrine surgeons.

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Citations

May 30, 2020·Endocrine Pathology·John Turchini, Anthony J Gill
Sep 18, 2020·Cancers·Devi D NelakurtiRuben C Petreaca
Jan 14, 2021·The Journal of International Medical Research·Yong Wang, Hui Zhang
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Jul 16, 2021·Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists·Edwina C MooreSusannah Ahern

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