Von-Hippel-Lindau (VHL) syndrome is characterized by focal vasoproliferative tumors of retinal capillaries called retinal capillary hemangioblastomas (RCH). These tumors are initially small and can be easily missed if not looked for carefully. As they grow, these tumors are more demanding to treat and hence the importance of detecting them early and treating them. Herein, we describe and review the optical coherence tomography angiography (OCTA) of the early-stage lesion, which suggested the involvement of superficial and a deeper retinal capillary plexus. In addition, to helping us detect these lesions earlier, OCTA may also help to understand the in vivo changes occurring at an earlier phase
Von hippellindau(VHL) disease being a rare genetic disorder, presents with broad spectrum of clinica...
Purpose: This prospective case series is aimed at exploring optical coherence tomographic angiograph...
Von Hippel-Lindau syndrome (VHL) is an autosomal dominant disease caused by a genetic aberration of ...
Von-Hippel-Lindau (VHL) syndrome is characterized by focal vasoproliferative tumors of retinal capil...
The aim of this study is to compare the optical coherence tomography angiography (OCTA) and fundus f...
PURPOSE:Von Hippel-Lindau (VHL) disease is a hereditary disorder that can lead to ophthalmic manifes...
A 21-year-old Chinese gentleman with no known medical illness, presented with a history of right pai...
Purpose: Only an endophytic growth pattern in juxtapapillary retinal hemangioblastoma (JRH) is an in...
Objectives: To present the multimodal imaging characteristics of precursor retinal angiomatous proli...
In this series, we discuss the role of optical coherence tomography angiography (OCTA) in assessing ...
Retinal hemangioblastoma (also referred to as retinal capillary hemangioma) is a benign lesion origi...
Objectives: To present the multimodal imaging characteristics of precursor retinal angiomatous proli...
To report the case of a small pigmented tumor in the macular region investigated using optical coher...
Von Hippel-Lindau (VHL) disease is a familial cancer syndrome characterized by benign or malignant t...
Purpose. To analyze the literature to determine the visual prognosis of eyes affected by retinal ang...
Von hippellindau(VHL) disease being a rare genetic disorder, presents with broad spectrum of clinica...
Purpose: This prospective case series is aimed at exploring optical coherence tomographic angiograph...
Von Hippel-Lindau syndrome (VHL) is an autosomal dominant disease caused by a genetic aberration of ...
Von-Hippel-Lindau (VHL) syndrome is characterized by focal vasoproliferative tumors of retinal capil...
The aim of this study is to compare the optical coherence tomography angiography (OCTA) and fundus f...
PURPOSE:Von Hippel-Lindau (VHL) disease is a hereditary disorder that can lead to ophthalmic manifes...
A 21-year-old Chinese gentleman with no known medical illness, presented with a history of right pai...
Purpose: Only an endophytic growth pattern in juxtapapillary retinal hemangioblastoma (JRH) is an in...
Objectives: To present the multimodal imaging characteristics of precursor retinal angiomatous proli...
In this series, we discuss the role of optical coherence tomography angiography (OCTA) in assessing ...
Retinal hemangioblastoma (also referred to as retinal capillary hemangioma) is a benign lesion origi...
Objectives: To present the multimodal imaging characteristics of precursor retinal angiomatous proli...
To report the case of a small pigmented tumor in the macular region investigated using optical coher...
Von Hippel-Lindau (VHL) disease is a familial cancer syndrome characterized by benign or malignant t...
Purpose. To analyze the literature to determine the visual prognosis of eyes affected by retinal ang...
Von hippellindau(VHL) disease being a rare genetic disorder, presents with broad spectrum of clinica...
Purpose: This prospective case series is aimed at exploring optical coherence tomographic angiograph...
Von Hippel-Lindau syndrome (VHL) is an autosomal dominant disease caused by a genetic aberration of ...