head and neck paragangliomas

GPTKB entity

Statements (50)
Predicate Object
gptkbp:instanceOf gptkb:disease
brain tumor
gptkbp:age adults
gptkbp:associatedWith SDH gene mutations
hereditary paraganglioma syndromes
gptkbp:canBe familial
sporadic
gptkbp:complication malignant transformation
cranial nerve dysfunction
vascular involvement
gptkbp:diagnosedBy gptkb:CT_scan
MRI
biopsy
angiography
gptkbp:firstDescribed early 20th century
gptkbp:gender female predominance
gptkbp:histology Zellballen pattern
https://www.w3.org/2000/01/rdf-schema#label head and neck paragangliomas
gptkbp:ICD-10_code gptkb:D35.6
gptkbp:location head
neck
gptkbp:marking gptkb:chromogranin_A
gptkb:S-100_protein
synaptophysin
gptkbp:maySecrete gptkb:catecholamines
gptkbp:originatedIn gptkb:paraganglionic_tissue
gptkbp:prevalence rare
gptkbp:rarelyMetastasize true
gptkbp:riskFactor family history
SDHB mutation
SDHC mutation
SDHD mutation
gptkbp:subspecies paraganglioma
Neuroendocrine Tumor
gptkbp:symptom hearing loss
cranial nerve palsy
pulsatile tinnitus
gptkbp:synonym gptkb:chemodectoma
glomus tumor
gptkbp:treatment astronomer
surgery
radiation therapy
gptkbp:website gptkb:carotid_body
vagal body
glomus jugulare
glomus tympanicum
jugulotympanic region
gptkbp:bfsParent gptkb:Hereditary_paraganglioma-pheochromocytoma_syndrome
gptkb:hereditary_paraganglioma-pheochromocytoma_syndrome
gptkbp:bfsLayer 8