TY - JOUR
TI - Evolution of a juxtapapillary von Hippel-Lindau tumour examined by optical coherence tomography
AU - Grigoropoulos, V.G.
AU - Nikolaidis, P.
AU - Emfietzoglou, I.
AU - Theodossiadis, P.G.
AU - Theodossiadis, G.P.
JO - Clinical and Experimental Optometry
PY - 2012
VL - 95
TODO - 2
SP - 237-240
PB - 
SN - 0816-4622, 1365-2230
TODO - 10.1111/j.1444-0938.2012.00720.x
TODO - adult;  article;  capillary hemangioma;  case report;  disease course;  hemangioblastoma;  human;  male;  optic nerve tumor;  optical coherence tomography;  pathology;  retina blood vessel;  von Hippel Lindau disease, Disease Progression;  Hemangioblastoma;  Hemangioma, Capillary;  Humans;  Male;  Optic Nerve Neoplasms;  Retinal Vessels;  Tomography, Optical Coherence;  von Hippel-Lindau Disease;  Young Adult
TODO - Purpose: The aim was to report the evolution of a case of von Hippel-Lindau (VHL) juxtapapillary retinal capillary haemangioblastoma (RCH) by optical coherence tomography (OCT3). Case report: The progress of a 24-year-old man suffering from VHL disease with a juxtapapillary haemangioblastoma and a small peripheral lesion was followed for 26.4 months with fundus photographs and OCT of the optic nerve head using the optic nerve head rim volume, ranging from 1.106 to 1.895mm 3. Visual acuity remained 6/6 throughout. Conclusions: OCT can be a useful tool in the follow up and decision-making of patients with small retinal capillary haemangioblastoma of the optic nerve. © 2012 The Authors. Clinical and Experimental Optometry © 2012 Optometrists Association Australia.
ER -