Novinky v diagnostice a léčbě MEN1

Title in English News in diagnostics and therapy of multiple endocrine neoplasia type 1
Authors

STARÝ Karel

Year of publication 2015
Type Article in Periodical
Magazine / Source Vnitřní lékařství
MU Faculty or unit

Faculty of Medicine

Citation
Field Other medical specializations
Keywords endosonography; chromogranin A; menin; multiple endocrine neoplasia type 1; neuroendocrine tumor; pituitary adenoma; primary hyperparathyroidism
Description MEN1 syndrome is an autosomal dominant disorder caused by mutation in the menin gene located on the 11th chromosome. It involves functional or cancerous diseases of parathyroid glands, hypophysis, endocrine pancreas, adrenal glands, or other tumors. The diagnosis of MEN1 is su¬spected if at least 2 components of this multiple tumor syndrome occur simultaneously. The increase in diagnostic precision enables detection of MEN1 in its early stages. Currently, the most frequently discussed topics include the use of biomarkers for diagnostics and new approaches in surgical treatment of MEN1.

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