Pheochromocytomas/paragangliomas are characterized by a unique molecular landscape
that allows their assignment to clusters based on underlying genetic alterations. With around …

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

Molecular targeted therapy plays an increasingly important role in the treatment of metastatic
pheochromocytomas and paragangliomas (PPGLs), which are rare tumors but remain …

Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors with
heterogeneous clinical presentations and potential lethal outcomes. The diagnosis is based …

Catecholamine-producing tumors of childhood include most notably neuroblastoma, but
also pheochromocytoma and paraganglioma (PPGL). Diagnosis of the former depends …

The mammalian adrenal gland is composed of two distinct tissue types in a bidirectional
connection, the catecholamine-producing medulla derived from the neural crest and the …

Cardiovascular disease (CVD) and cancer are collectively responsible for tens of millions of
global deaths each year. These rates are projected to intensify as the COVID-19 pandemic …

Purpose To identify presurgical and surgical risk factors for postsurgical complications in the
pheochromocytoma surgery. Methods A retrospective study of pheochromocytomas …

Abstract Objective Head-neck paragangliomas (HNPGLs) are rare tumors with
approximately half arising due to germline pathogenic variants (PVs) in succinate …

Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors arising
from chromaffin cells of the adrenal medulla or extra-adrenal paraganglia, respectively …