Patients with germline SDHD pathogenic variants (encoding succinate dehydrogenase
subunit D; ie, paraganglioma 1 syndrome) are predominantly affected by head and neck …

Pheochromocytoma and paraganglioma (PPGL) require prompt consideration and efficient
diagnosis and treatment to minimize associated morbidity and mortality. Once considered …

Adrenal emergencies are pathologic states that can cause significant morbidity and mortality
among emergency department (ED) patients. Most of them are relatively uncommon as …

Phaeochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumours with
a strong genetic predisposition, involving over 20 genes and with germline pathogenic …

Abdominal pheochromocytomas and paragangliomas (PPGLs) are characterized by the
overproduction of catecholamines, which are associated with hemodynamic instability (HDI) …

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

Context Biological sex can play a role in the severity of certain diseases. Objective Our
objective was to evaluate whether sex-related differences affect the signs and symptoms of …

Pheochromocytoma and paragangliomas (PPGLs) originate from the chromaffin cells of the
adrenal medulla or neural crest progenitors outside the adrenal gland, respectively. The …

Background In humans with pheochromocytomas (PCCs), targeted metabolomics is used to
determine the catecholamine phenotype or to uncover underlying pathogenic variants in …

Tympanojugular paragangliomas (TJP) originate from the parasympathetic ganglia in the
lateral base of the skull. Although the cellular composition and oncogenic mechanisms of …