Phaeochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumours that
arise not only in adulthood but also in childhood and adolescence. Up to 70–80% of …

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 Criteria for the pathological classification of adult adrenocortical tumours
(ACTs) have been found to overestimate the malignant potential of childhood ACTs. We …

The spectrum of adrenal masses in the pediatric population markedly differs from that in the
adult population. Imaging plays a crucial role in detecting adrenal masses, differentiating …

Objectives The aim of the study was to evaluate the CT features of adrenal tumors in an
effort to identify features specific to pheochromocytomas and second, to define a feasible …

Simple Summary Adrenocortical tumors are rare neoplasms with an uncertain prognosis. A
greater understanding of the biology of these tumors will allow new therapeutic targets to be …

Pediatric adrenocortical tumors are rare and heterogeneous endocrine malignancies.
Objectives To report clinical, biochemical, and histological features, staging, and therapeutic …

A nonspecific clinical picture and the course of Conn syndrome — current findings in the
screening program for hypertensiv Page 1 189 www.ah.viamedica.pl Copyright © 2023 Via …

В статье приводятся данные по оценке фертильной функции у пациенток с АКТГ-
секретирующими аденомами гипофиза в Республике Узбекистан. Раскрываются …

A drenocortical carcinoma (ACC) in infancy is a serious disease of poor prognosis if the
diagnosis is not promptly recognized. Surgical treatment with complete tumor removal is the …