Interventions: The patient underwent parathyroid tumor resection and metastasis biopsy.
Outcomes: The patient received denosumab and sorafenib treatment. Lessons: As an …

Background To evaluate the outcome of duodenopancreatic reoperations in patients with
multiple endocrine neoplasia type 1 (MEN1). Methods MEN1 patients who underwent …

Background The multiple endocrine neoplasia type 1 syndrome (MEN1) natural history is
poorly evaluated, and few single-institution experiences about hereditary …

BACKGROUND: Approximately 10% of patients with primary hyperparathyroidism (PHPT)
have hereditary disease. Hereditary PHPT may be syndromic (MEN1, 2, and 4 and …

ABSTRACT Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare autosomal dominantly
inherited endocrine tumor predisposition syndrome, caused by mutations in the MEN1 gene …

Animal models of cancer have been instrumental in advancing our understanding of the
biology of tumor initiation and progression, in studying gene function and in performing …

Prospective randomized data are lacking, but current clinical expert guidelines recommend
annual screening examinations, including laboratory assessments and various imaging …

В статье представлен проект клинических рекомендаций по диагностике и лечению
первичного гиперпаратиреоза у взрослых пациентов, в котором приведен …

Purpose of review Neuroendocrine tumors (NETs) were initially identified as a separate
entity in the early 1900s as a unique malignancy that secretes bioactive amines. GI-NETs …

Over the past few decades, the worldwide incidence of cutaneous melanoma, a malignant
neoplasm arising from melanocytes, has been increasing markedly, leading to the highest …