Ontology highlight
ABSTRACT: Background
Hemangioblastoma (HB) is a rare and highly vascularized tumor that originates from the central nervous system as well as other part of the body. They can appear sporadically or as part of von Hippel-Lindau (VHL) disease, a rare hereditary cancer syndrome. Although surgery can cure the majority of HBs, the disease shows a treatment-refractory challenge upon recurrence. HBs express a high amount of vascular endothelial growth factor (VEGF) which is responsible for angiogenesis and subsequently tumor progression. Anti-angiogenic treatment like bevacizumab has showed effect on HB, so we hypothesized that anlotinib could trigger HB regression via its inhibitory effect on VEGF.Case presentation
We will share our experience in treating a 62-year-old woman with mu
SUBMITTER: Jin N
PROVIDER: S-EPMC9092942 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature