Results 21 to 30 of about 1,633 (148)
Medicina (Lithuania)Background and Objectives: Here, we report the anatomical and functional outcomes of Pars Plana Vitrectomy (PPV) with feeder vessel ligation, with or without endoresection in cases of retinal detachment (RD) secondary to retinal capillary ...
Marco Mura +2 more
exaly +3 more sources
Retinal Hemangioblastoma with Extraocular Extension: Report of Three Cases. [PDF]
Ocul Oncol Pathol, 2021 Retinal hemangioblastoma (RH) is the earliest and most common clinical manifestation in Von Hippel-Lindau (VHL) disease. RH can also present in isolation without any evidence of VHL. Clinical course of RH can be stationary or progress to exudation and chronic retinal detachment requiring surgical intervention.
Kumari N, Das S, Bhaduri A, Gandhi A.
europepmc +4 more sources
Photocoagulation for retinal hemangioblastoma in Von Hippel-Lindau disease [PDF]
Srpski Arhiv za Celokupno Lekarstvo, 2023 Introduction. Von Hippel–Lindau disease is a hereditary, autosomal dominant, tumor syndrome with a predisposition to developing various benign and malignant tumors. Retinal hemangioblastoma is often the presenting manifestation.
Vasilijević Jelena +4 more
doaj +1 more source
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
MANAGEMENT OF RETINAL HEMANGIOBLASTOMA IN VON HIPPEL-LINDAU DISEASE. [PDF]
Retina, 2019 Purpose: To review the current state of diagnosis and management of retinal hemangioblastoma and retinal vascular proliferation arising from von Hippel–Lindau (VHL) disease. Methods: A review of the literature was performed.
Wiley HE +7 more
europepmc +6 more sources
Aggressive-fungating retinal hemangioblastoma
Journal of Cancer Research and Therapeutics, 2021 Retinal hemangioblastomas are one of the most common and early manifestations of Von Hippel–Lindau disease. Early detection is the key in their management. When left untreated, these benign neoplasms may continue to grow and result in scleral infiltration and extraocular extension warranting enucleation of the globe.
Sudha Girish, Menon +4 more
openaire +2 more sources
Oman Journal of Ophthalmology, 2022 A 6-year-old girl with visual impairment in the right eye (OD) was referred for an eye evaluation. The fundus of the OD showed a fibrotic orange endophytic lesion located adjacent to the optic disc.
Franco Benvenuto +4 more
doaj +1 more source
Montage Error in Ultra-Widefield Imaging of Retinal Hemangioblastomas. [PDF]
Case Rep Ophthalmol MedA 20‐year‐old male presented with three large retinal hemangioblastomas in the left eye. At the 5‐week follow‐up, automated montage ultra–widefield imaging appeared to demonstrate a fourth lesion, suggesting possible disease progression. Clinical examination, however, confirmed the presence of only three tumors.
Belmouhand M, Kiilgaard JF, Faber C.
europepmc +2 more sources
Phenotypic and Genotypic Features of a Chinese Cohort with Retinal Hemangioblastoma. [PDF]
Genes (Basel)Purpose: To delineate the genotype and phenotype of RH in a Chinese cohort. Methods: A group of 51 Chinese probands with RH across 76 eyes was assembled and underwent complete retinal imaging examinations. Sanger sequencing and universal primer quantitative fluorescent multiplex–polymerase chain reaction (UPQFM-PCR) were employed for mutation detection
Gao L +8 more
europepmc +3 more sources
Von Hippel-Lindau Syndrome: Medical Syndrome or Surgical Syndrome? A Surgical Perspective
Journal of Kidney Cancer and VHL, 2021 Von Hippel-Lindau syndrome (VHL) is an autosomal dominant disease caused by a genetic aberration of the tumor suppressor gene VHL and characterized by multi-organ tumors.
Danilo Coco, Silvana Leanza
doaj +1 more source