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 (ACC) is a heterogenous group of diseases with different clinical
behaviour between adult and paediatric patients. In addition, three histological variants …

Adrenocortical carcinoma (ACC) is a rare endocrine malignancy of the adrenal gland with
an unfavorable prognosis. It is rare in the pediatric population, with an incidence of 0.2-0.3 …

Childhood adrenocortical tumors (ACTs) are rare, representing∼ 0.2% of all pediatric
malignancies and having an incidence of 0.2–0.3 new cases per million per year in the …

Adrenocortical tumors (ACT) in the adult and pediatric population are generally considered
distinct entities due to differences in molecular events related to tumorigenesis, clinical …

Adrenocortical carcinoma (adrenal cortex‑derived cancer), an orphan malignancy, is a very
aggressive disease that affects both adults and children with an annual incidence of 1‑2 …

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

The rarity of this disease makes it a real challenge. Here, we present a review focusing on
clinical practice. A methodic approach aiming to clarify the diagnosis and a follow-up are …

Simple Summary Pediatric adrenocortical tumors are rare. Little information is available on
the incidence, risk factors, prognostic factors, treatment, and overall survival. In this …

Background and Aims: Pediatric adrenocortical tumors (ACTs) are very rare endocrine
neoplasms in childhood. In this study, we performed a retrospective analysis of children with …