Photodynamic Therapy in Ocular Oncology [PDF]
Journal of Ophthalmic & Vision Research, 2020 Over the past two decades, we have witnessed the increasing use of photodynamic therapy (PDT) in the field of ocular oncology. Based on a review of the literature and our own experience, we herein review the role of PDT for the management of intraocular ...
Mehdi Mazloumi +7 more
doaj +2 more sources
Aggressive retinal hemangioblastoma with scleral penetration in Von-Hippel-Lindau syndrome
Indian Journal of Ophthalmology. Case Reports, 2021 Retinal hemangioblastoma is associated with Von-Hippel–Lindau syndrome. Here, we report the case of a 50-year-old man who had a retinal hemangioblastoma that penetrated the sclera and presented as an extra-ocular mass.
Ferzana Mohammed +3 more
doaj +3 more sources
Clinical and molecular characteristics of East Asian patients with von Hippel–Lindau syndrome
Chinese Journal of Cancer, 2016 Background Von Hippel–Lindau (VHL) syndrome is a dominantly inherited multisystem cancer syndrome caused by a heterozygous mutation in the VHL tumor suppressor gene.
Meihua Wong +6 more
doaj +2 more sources
Association of mutations and polymorphic variants of the VHL gene with the clinical characteristics of retinal capillary hemangioma [PDF]
Российский офтальмологический журнал, 2019 Purpose. To study the association of mutations and polymorphic variants of the VHL gene with the clinical characteristics of retinal capillary hemangioma.Material and methods.
V. V. Neroev +7 more
doaj +2 more sources
Successful Management of a Solitary Retinal Capillary Hemangioblastoma in a Stepwise Approach
Delhi Journal of OphthalmologyRetinal capillary hemangioblastoma (RCH) is a vascular tumor often associated with Von Hippel–Lindau disease. Solitary RCHs are rare. We report a case of an adolescent boy with sporadic solitary RCH presenting with RCH-associated exudative retinal ...
Shruti Nair +3 more
doaj +2 more sources
Concurrent Von Hippel-Lindau disease and enhanced S-cone syndrome leading to a distinct retinal phenotype [PDF]
American Journal of Ophthalmology Case ReportsBackground: Von Hippel–Lindau (VHL) disease and Enhanced S-cone syndrome (ESCS) are rare inherited disorders that independently predispose to vision-threatening retinal pathology through distinct mechanisms: VHL through hypoxia-induced activation of ...
Maram AlEnazi +3 more
doaj +2 more sources
Clinical and Genetic Characteristics of Retinal Capillary Hemangioblastoma in Korean Patients. [PDF]
Korean J Ophthalmol, 2022 Purpose: We investigated the clinical features of Korean patients with retinal capillary hemangioblastoma (RCH) and genetic variants of the von Hippel-Lindau (<i>VHL</i>) gene.Methods: A retrospective analysis was performed on patients with RCH from 2003 to 2021 at Seoul National University Bundang Hospital.
Lee SH, Park KH, Woo SJ, Park SJ, Joo K.
europepmc +3 more sources
Retinal detachment risk in a cohort of von Hippel-Lindau patients at a Major U.S. tertiary care facility [PDF]
AJO InternationalPurpose: To report the retinal findings, cumulative incidence of retinal capillary hemangioblastoma (RCH), retinal detachment (RD) outcomes, and risk factors in a large cohort of von Hippel-Lindau (VHL) patients within a major U.S. Tertiary Care Facility.
Konstantinos G. Baroutis +5 more
doaj +2 more sources
RETINAL Cases & Brief ReportsPurpose: Retinal capillary hemangioblastoma is present in about half of the carriers of the von Hippel–Lindau gene mutation and can lead to the evolution of blindness. Herewith is a proposal for surgical intraretinal feeder vessel ligature to induce ischemia of the phakoma and to resolve the exudative secondary retinal ...
Gallenga, Carla E. +6 more
openaire +3 more sources
Laser Speckle Flowgraphy in Juxtapapillary Retinal Capillary Hemangioblastoma: A Case Report on Natural Course and Therapeutic Effect [PDF]
Oncotarget, 2020 Susumu Ishida +2 more
exaly +2 more sources