Background Cross-sectional imaging regularly results in incidental discovery of adrenal
tumours, requiring exclusion of adrenocortical carcinoma (ACC). However, differentiation is …

Context: Pituitary adenomas and pheochromocytomas/paragangliomas (pheo/PGL) can occur
in the same patient or in the same family. Coexistence of the two diseases could be due to …

Platelets play a critical role in vascular inflammation through the podoplanin and collagen/fibrin
receptors, C-type-lectin-like-2 (CLEC-2) and glycoprotein VI (GPVI), respectively. Both …

Despite the established role of Ki67 labeling index in prognostic stratification of adrenocortical
carcinomas and its recent integration into treatment flow charts, the reproducibility of the …

Background Causes of “true” late kidney allograft failure remain unclear as study selection
bias and limited follow-up risk incomplete representation of the spectrum. Methods We …

Objective Adrenocortical carcinoma (ACC) is a rare aggressive malignancy with
heterogeneous clinical outcomes. Recent studies proposed a combination of clinical/histopathological …

Background Alström syndrome (AS) is a rare autosomal recessive ciliopathy with a wide
spectrum of clinical features, including cone–rod retinal dystrophy, neuronal deafness, severe …

We report the clinical outcomes of eleven patients with succinate dehydrogenase subunit A (SDHA)
germline mutations from three UK tertiary referral centres to highlight a more diverse …

Symptomatic pituitary adenomas occur with a prevalence of approximately 0.1% in the general
population. It is estimated that 5% of pituitary adenomas occur in a familial setting, either …

… g ; Iacucci, Marietta a,,b,,c ; Cooney, Rachel d ; Ghosh, Subrata a,,b,,c,,* ; Skordilis, Kassiani
e,,* … * Kassiani Skordilis and Subrata Ghosh contributed equally to the writing of this article. …