In this review, we detail the changes and the relevant features that are applied to
neuroendocrine neoplasms (NENs) in the 2022 WHO Classification of Endocrine and …

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

Simple Summary Adrenocortical carcinoma is a rare cancer with a poor prognosis. Adrenal
tumors are, however, commonly identified in clinical practice. Discrimination between …

Methods A working group established by ESES reviewed the current guidelines and
undertook a literature search of the PubMed database focused on several clinical questions …

Adrenocortical neoplasms are rare in childhood. Their histopathological categorization into
benign and malignant is often challenging, impacting further management. While the …

BACKGROUND Oncocytic adrenocortical tumor (OACT) is rare, with few cases reported in
the literature. No more than 20 cases in children have been reported. The clinical …

Hyperandrogenism is a state of androgen excess that can induce hirsutism and
oligo/amenorrhea in women of reproductive age. Therapeutic strategies differ according to …

Adrenal cortical eosinophilic adenoma usually presents as non‑functional adrenal tumor but
may lead to Cushing's syndrome in patients. The present article reports a patient with …

Background: Oncocytic adrenal neoplasms, defined by≥ 90% of oncocytic cells, are rare.
The significance of oncocytic changes within an adrenal neoplasm remains unclear …

Abstract Background Oncocytic adrenocortical neoplasms (OANs) are rare endocrine tumors
that present as a spectrum from benign to malignant. The outcomes after surgical resection …