Paragangliomas make up a family of neoplasms that develop from the paraganglia tissues,
which are themselves of neural crest origin and have similar functions and histologic …

Head and neck paragangliomas (HNPGLs) are rare neuroendocrine tumors typically arising
from nonsecretory head and neck parasympathetic ganglia. Historically thought of as …

Despite the established role of SDHB/SDHA immunohistochemistry as a valuable tool to
identify patients at risk for familial succinate dehydrogenase-related pheochromocytoma …

Objective Although the succinate dehydrogenase (SDH)-related tumor spectrum has been
recently expanded, there are only rare reports of non-pheochromocytoma/paraganglioma …

The management of head and neck paragangliomas (HNPGLs) has changed significantly in
recent years. There is, however, an absence of guidance in the literature regarding the …

Recent advances in molecular genetics and genomics have led to increased understanding
of the aetiopathogenesis of pheochromocytomas and paragangliomas (PPGLs). Thus, pan …

Summary Pheochromocytomas (PHEOs) and paragangliomas (PGLs) are neuroendocrine
tumors that express somatostatin receptors (SSTRs), a phenomenon that constitutes a basis …

Background: Recommendations regarding head and neck paragangliomas (HNPGL) have
undergone a fundamental reorientation in the last decade as a result of increased …

Summary Background and objectives The International Collaboration on Cancer Reporting
(ICCR) is a not-for-profit to develop evidence-based, internationally agreed-upon …

Over the past two decades advances in genomic technologies have transformed knowledge
of the genetic basis of phaeochromocytoma and paraganglioma (PPGL). Though traditional …