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

A molecular biology–based taxonomy has been proposed for pheochromocytoma and
paraganglioma (PPGL). Data from the Cancer Genome Atlas revealed clinically relevant …

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

Pheochromocytomas and paragangliomas (PCC/PGLs) are rare, mostly catecholamine-
producing neuroendocrine tumors of the adrenal gland (PCCs) or the extra-adrenal …

Disregarding the widely used division of skull base into anterior and lateral, since the skull
base should be conceived as a single anatomic structure, it was to our convenience to group …

Background Carotid body tumor (CBT) is a rare neoplasm that has been increasingly
studied during the last decades; nevertheless, it continues to be a topic of controversy. This …

In the era of precision medicine, radiation medicine is currently focused on the precise
delivery of highly conformal radiation treatments. However, the tremendous developments in …

Background The study aims to conduct a review of the surgical management of carotid body
tumor. Methods Consecutive patients with CBT who received surgical interventions from …

Background Radiation to the head and neck is a well‐established risk factor for the
development of carotid artery stenosis. Our objective was to identify the prevalence …

Objective To characterize the recurrence of head and neck paragangliomas and the factors
associated with disease progression after treatment. Study Design Retrospective cohort …