New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense Mutations.
Gustavo F C FagundesJanaina PetenuciDelmar M LourencoEricka B TrarbachMaria Adelaide A PereiraJoya Emilie Correa D'EurAna O HoffAntonio M LerarioMaria Claudia N ZerbiniSheila SiqueiraFernando YamauchiVictor SrougiFabio Y TannoJose Luis ChamboAna Claudia LatronicoBerenice B MendoncaMaria Candida B V FragosoMadson Queiroz AlmeidaPublished in: Journal of the Endocrine Society (2019)
VHL missense mutations were highly associated with PHEO and PNETs. Our data support that in children with VHL harboring missense mutations, biochemical screening for PHEO should be initiated at diagnosis.