Pheochromocytoma and Paraganglioma Pheochromocytoma and paraganglioma are
related tumors that differ mainly in location; pheochromocytomas are adrenal, and …

Pheochromocytomas are rare neuroendocrine tumors that produce and store
catecholamines. Without adequate preparation, the release of excessive amounts of …

Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors that
arise from chromaffin cells of the adrenal medulla and the sympathetic/parasympathetic …

This article aims to review current concepts in diagnosing and managing
pheochromocytoma and paraganglioma (PPGL). Personalized genetic testing is vital, as 40 …

Background Phaeochromocytoma or paraganglioma (collectively known as PPGL) in
pregnant women can lead to severe complications and death due to associated …

Multiple endocrine neoplasia type 2 (MEN2) is a neuroendocrine cancer syndrome
characterized by medullary thyroid carcinoma, in combination or not with …

Trace-level detection of Dopamine (DA) in human body fluids is crucial for diagnosing
neurological disorders, understanding mental health, and advancing drug discovery, but …

Background To evaluate the feasibility and safety of robot-assisted retroperitoneal
laparoscopic adrenalectomy (RARLA) for large pheochromocytomas (PHEOs; size≥ 6 cm) …

Introduction To describe outcomes of patients with metyrosine (MET) pretreatment for
abdominal surgical resection of pheochromocytoma or paraganglioma (PCC/PGL) …

Objective Pheochromocytoma is a rare neuroendocrine tumour that secretes
catecholamines and originates in the adrenal gland. Although surgical resection is the only …