Mathematical modeling and simulation of tumor-induced angiogenesis in retinal hemangioblastoma. [PDF]
PLoS Computational BiologyRetinal Hemangioblastoma (RH) is the most frequent manifestation of the von Hippel-Lindau syndrome (VHL), a rare disease associated with the germline mutation of the von Hippel-Lindau protein (pVHL).
Franco Pradelli +5 more
doaj +5 more sources
Parapapillary retinal hemangioblastoma presenting as an epiretinal membrane in a patient with Von Hippel–Lindau disease: a case report [PDF]
Frontiers in MedicineBackgroundRetinal hemangioblastoma (RH) is a benign, highly vascularized tumor arising from the neurosensory retina. It may occur sporadically or as a manifestation of Von Hippel–Lindau (VHL) disease.
Licong Liang +3 more
doaj +2 more sources
Von Hippel-Lindau syndrome presenting as a lateral ventricular space-occupying lesion: a case report [PDF]
Frontiers in OncologyVon Hippel-Lindau disease is a rare autosomal dominant genetic disorder caused by mutations in the VHL tumor suppressor gene located on chromosome 3.
Lu Liu +7 more
doaj +2 more sources
Juxtapapillary retinal hemangioblastoma remission in a von Hippel-Lindau patient treated with cabozantinib [PDF]
American Journal of Ophthalmology Case ReportsPurpose: To describe a unique case of von Hippel-Lindau (VHL) disease in which a treatment-resistant juxtapapillary retinal hemangioblastoma (RH) underwent complete and sustained regression following systemic therapy with cabozantinib, a VEGFR/MET ...
Mauro Sartore +4 more
doaj +2 more sources
Oral belzutifan treatment in von hippel-lindau-associated retinal hemangioblastoma: a promising approach [PDF]
International Journal of Retina and VitreousBackground Von Hippel-Lindau (VHL)-associated retinal hemangioblastomas (RHs) may cause vision-threatening exudation and hemorrhage. Conventional local therapies may be limited in advanced, recurrent, or anatomically high-risk lesions.
Adnan Kilani +7 more
doaj +2 more sources
Von Hippel-Lindau Disease: The Importance of Retinal Hemangioblastomas in Diagnosis
Türk Oftalmoloji Dergisi, 2017 Von Hippel-Lindau (VHL) disease is a familial cancer syndrome characterized by benign or malignant tumors which may involve more than one system. Retinal hemangioblastomas are usually the initial manifestation of VHL disease and can cause vision loss.
Sevinç Şahin Atik +6 more
doaj +5 more sources
Retinal Hemangioblastoma in a Patient With Von Hippel-Lindau Disease: A Case Report and Literature Review [PDF]
Frontiers in Oncology, 2022 Xionggao Huang, Yikeng Huang, Weiwen Hu
exaly +2 more sources
Case Report: The cystic masquerade in type 1 Von Hippel-Lindau disease: coexisting clear cell renal cell carcinoma and an imaging-suspected pancreatic neuroendocrine tumor [PDF]
Frontiers in OncologyVHL disease is a rare autosomal dominant tumor predisposition syndrome characterized by the development of cystic and solid lesions in multiple organs.
Daiyu Yang, Yinghao Sun, Shengyu Zhang
doaj +2 more sources
Imaging features of retinal hemangioblastoma: A case report. [PDF]
World J Clin Cases, 2023 Hemangioblastoma typically occurs in the cerebellum, spinal cord, and central nervous system. However, in rare cases, it could occur in the retina or optic nerve. The prevalence of retinal hemangioblastoma is 1 in 73080, and it occurs either alone or as the manifestation of von Hippel Lindau (VHL) disease. Here, we reported a rare case with the imaging
Tang X, Ji HM, Li WW, Ding ZX, Ye SL.
europepmc +3 more sources
Belzutifan-Induced Regression of Retinal Capillary Hemangioblastoma: A Case-Series
American Journal of Ophthalmology Case ReportsPurpose: To report a series of three patients with von Hippel-Lindau (VHL) disease who demonstrated regression of their retinal hemangioblastomas (RH) using belzutifan in conjunction with photocoagulation therapy.
Sami H Uwaydat +2 more
exaly +3 more sources