Adrenal cysts are uncommon and usually asymptomatic, and therefore are usually
incidentally discovered adrenal lesions. They have a broad pathohistological spectrum that …

Radiotheranostics utilizes a set of radioligands incorporating diagnostic or therapeutic
radionuclides to achieve both diagnosis and therapy. Imaging probes using diagnostic …

Abstract Introduction Von Hippel-Lindau disease (eg VHL) is an autosomal dominant multi-
organ cancer syndrome caused by a mutation in the VHL tumour suppressor gene. In this …

Los feocromocitomas son tumores neuroendocrinos poco frecuentes que derivan de las
células cromafines de la medula adrenal y que secretan catecolaminas. La medición de las …

Background Despite recent improvements in perioperative outcomes after
pheochromocytoma resection, hemodynamic instability (HI) remained of high concern. The …

Background Pheochromocytoma is a rare disease, and its familial occurrence is quite
uncommon. The aim of this paper is to report a three-generation phenotypical expression of …

Background: Pheochromocytoma and paraganglioma (PPGL) are considered a curable
cause of secondary hypertension. However, some studies identified a considerable ratio of …

Diagnosis of pheochromocytoma, a rare, largely-incidentally found tumor of the adrenal
glands, is typically challenging due to its frequently variable, nonspecific, and atypical …

Pheochromocytomas are rare tumours that arise from neural crest cells of the adrenal
medulla. They commonly secrete catecholamines and other biological peptides that account …