Pheochromocytomas (PCCs) and paragangliomas (PGLs) are rare neuroendocrine tumors
of the adrenal glands and the sympathetic and parasympathetic paraganglia. They can …

Phaeochromocytomas and paragangliomas (PPGLs) are neural-crest-derived tumours of
the sympathetic or parasympathetic nervous system that are often inherited and are …

Objective: The aim was to formulate clinical practice guidelines for pheochromocytoma and
paraganglioma (PPGL). Participants: The Task Force included a chair selected by the …

Objective Head and neck paragangliomas are a group of slow-growing hypervascular
tumors associated with the paraganglion system. The approach to evaluate and treat these …

Pheochromocytomas (PCCs) and paragangliomas (PGLs) are catecholamine-secreting
tumors of neural crest origin. Once collectively known as the '10% tumor', based on the …

BACKGROUND Pheochromocytomas are rare catecholamine-producing tumors derived in
more than 30% of cases from mutations in 9 tumor-susceptibility genes identified to date …

Multiple endocrine neoplasia type 2 is historically composed of three clinical subtypes, all of
which are associated with germline mutations in the RET proto-oncogene. Multiple …

Purpose Choroid plexus carcinomas are pediatric tumors with poor survival rates and a
strong, but poorly understood, association with Li-Fraumeni syndrome (LFS). Currently, with …

Pheochromocytomas are catecholamine producing neuroendocrine tumors that can be
adrenal or extra-adrenal in origin. The classic symptoms of pheochromocytoma are …

Background Nowadays, 65–80% of pheochromocytoma and paraganglioma (PPGL) cases
are explained by germline or somatic mutations in one of 22 genes. Several genetic testing …