Adrenocortical carcinoma (ACC) is a rare endocrine malignancy, often with an unfavorable
prognosis. Here we summarize the knowledge about diagnosis, epidemiology …

Clinically inapparent adrenal masses are incidentally detected after imaging studies
conducted for reasons other than the evaluation of the adrenal glands. They have frequently …

The NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for Neuroendocrine
and Adrenal Gland Tumors focus on the diagnosis, treatment, and management of patients …

Adrenocortical carcinoma is a rare heterogeneous neoplasm with an incompletely
understood pathogenesis and a poor prognosis. Previous studies have identified …

Purpose We created a registry for pediatric adrenocortical tumors (ACTs), which are rare
and are not well characterized. We provide a descriptive analysis of 254 patients registered …

Adrenal carcinoma in children is associated with virilism and a less aggressive natural
history; in adults it presents as a mixed Cushing‐virilizing syndrome and has a virulent …

Adrenocortical carcinomas are rare, highly malignant tumors that account for only 0.2% of
deaths due to cancer. Given the limited number of patients seen in most medical centers …

Background: One of the key issues in the treatment of adrenocortical carcinoma is the
efficacy of repeat resection of local recurrence and metastatic disease in affected patients …

Epithelial-to-mesenchymal transition (EMT) is an essential mechanism for development and
wound healing, but in cancer it also mediates the progression and spread of aggressive …

Neuroendocrine tumors comprise a broad family of tumors, the most common of which are
carcinoid and pancreatic neuroendocrine tumors. The NCCN Neuroendocrine Tumors …