An adrenal incidentaloma is now established as a common endocrine diagnosis that
requires a multidisciplinary approach for effective management. The majority of patients can …

Simple Summary Pheochromocytoma and paraganglioma (together PPGL) are rare
neuroendocrine tumors that arise from chromaffin tissue and produce catecholamines …

Importance Neurofibromatosis type 1 (NF1) is a complex genetic disorder that is associated
with not only neurofibromas, but also an increased susceptibility to other neoplasms …

Abstract Context Pheochromocytomas and paragangliomas (PPGLs) are known to be rare.
However, there is scant literature reporting their epidemiology, particularly whether the …

Opinion statement The incidence of metastatic pheochromocytoma (PHEO) and
paraganglioma (PGL) may occur in as many as 35% of patients particularly with PGL and …

Background With the increasing access to imaging more pheochromocytomas are
diagnosed in the workup of adrenal incidentalomas. This may have changed the occurrence …

Excess of catecholamines in pheochromocytoma is usually accompanied with classical
symptoms and signs. In some cases, severe cardiovascular complications (eg, heart failure …

Context: Pheochromocytoma crisis is a feared and potentially lethal complication of
pheochromocytoma. Objective: We sought to determine the best treatment strategy for …

Adrenalectomy for pheochromocytoma is reported with a mortality close to zero in recent
studies. The dogma of preoperative fluid and hypotensive drug administrations is widely …

Background Resection of pheochromocytoma is often associated with hemodynamic
instability (HDI). We examined patient and tumor factors that may influence HDI. The effect of …