The new WHO classification of adrenal cortical proliferations reflects translational advances
in the fields of endocrine pathology, oncology and molecular biology. By adopting a …

Adrenocortical carcinoma is a rare malignancy with an annual worldwide incidence of 1–2
cases per 1 million and a 5-year survival rate of< 60%. Although adrenocortical carcinoma is …

Purpose This study aimed to investigate the genetic cause of food-dependent Cushing
syndrome (FDCS) observed in patients with primary bilateral macronodular adrenal …

Follicular thyroid tumors pose a diagnostic challenge on the preoperative level, as the
discrimination between follicular thyroid carcinoma (FTC) and adenoma (FTA) demands …

Adrenal cortical carcinoma (ACC) is a rare and aggressive malignancy that poses
challenging issues regarding the diagnostic workup. Indeed, no presurgical technique or …

Simple Summary Neuroendocrine tumors are a collection of neoplastic lesions arising in
cells with traits similar to hormone-producing and nerve cells with the ability to secrete …

Mutational inactivation of the DICER1 gene causes aberrant micro-RNA maturation, which in
turn may have consequences for the posttranscriptional regulation of gene expression …

Abstract Adrenal paraganglioma (or “pheochromocytoma”) and extra-adrenal
paraganglioma, collectively abbreviated PPGL, are rare but spectacular nonepithelial …

Non-coding RNAs (ncRNAs) are a type of genetic material that do not encode proteins but
regulate the gene expression at an epigenetic level, such as microRNAs (miRNAs) and long …

Bilateral macronodular adrenocortical disease (BMAD) is a neoplastic disease associated
with a high frequency of germline disease. Armadillo repeat containing 5 (ARMC5) …