| Literature DB >> 26497655 |
Denis Migliorini1, Sven Haller2, Doron Merkler3, Angela Pugliesi-Rinaldi1, Avinash Koka4, Karl Schaller4, Beatrice Leemann1, Pierre-Yves Dietrich1.
Abstract
Hemangioblastoma is a rare benign neoplasm, accounting for less than 2% of all primitive brain tumors. It may arise sporadically in a solitary form, or associated with Von Hippel-Lindau (VHL) disease with multiple tumors. Surgery is the mainstay treatment, but management is challenging in case of recurrent and/or multiple tumors. VHL protein is defective in both forms of hemangioblastoma, leading to the accumulation of hypoxia-inducible factor, stimulating angiogenesis via VEGF and PDGF mainly. Here, we report a 37-year-old woman's case with recurrent and rapidly progressive VHL-associated hemangioblastomas, causing severe disability. She was treated 24 months with pazopanib, a multityrosine kinase inhibitor (TKI) targeting VEGF and PDGF-β pathways. Despite moderate radiological changes, progressive improvement in her clinical condition persisting over 3 years was observed. Inhibiting angiogenesis is a therapeutic option that may improve the quality of life and the autonomy of VHL patients disabled with multiple hemangioblastomas.Entities:
Keywords: Von Hippel–Lindau disease; hemangioblastoma; pazopanib
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Year: 2015 PMID: 26497655 PMCID: PMC6083944 DOI: 10.2217/cns.15.22
Source DB: PubMed Journal: CNS Oncol ISSN: 2045-0907