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[Multiple endocrine neoplasia type 1: about a case]

Gladys Anguezomo1,2, Ghizlane El Mghari1,2, Nawal El Ansari1,2

  • 1Service d'Endocrinologie, Diabétologie et Maladies Métaboliques, CHU Mohamed VI Marrakech, Maroc.

The Pan African Medical Journal
|November 7, 2019
PubMed
Summary

Multiple endocrine neoplasia type 1 (MEN1) presented as an aggressive pituitary tumor. This rare genetic disorder later manifested with hyperparathyroidism and pancreatic neuroendocrine tumors, highlighting a unique clinical progression.

Keywords:
Néoplasie endocrinienne multiple type1 (NEM1)adénome hypophysairehyperparathyroïdiepNET

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