Correspondence to: Dr B E Baysal, Departments of Psychiatry, Otolaryngology, and Human Genetics. The University of Pittsburgh Medical Center, 3811 O’Hara Street R1445, Pittsburgh, PA, 15213, USA; ...

the diagnostic workup focused on identifying possible hereditary syndromes linked to paragangliomas and phaeochromocytomas. The high levels of normetanephrine pointed towards a catecholamine-secreting ...

The patient underwent surgery, which confirmed a malignant neck paraganglioma with metastasis to a cervical lymph node. He had no family history of carotid body tumors or pheochromocytoma.

Familial paraganglioma-pheochromocytoma syndrome is a hereditary condition indicated by the presence of tumors called paragangliomas and/or pheochromocytomas. Paranganglioma tumors arise from bundles ...

Priority review for Welireg is based on data from the Phase II LITESPARK-015 trial, which showed promising response rates in patients with advanced, unresectable, or metastatic pheochromocytoma and ...