April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Melanocytoma of the Optic Disk Associated With Visual Field Defect: Clinical Features and Imaging Using Spectral Domain Optical Coherence Tomography
Author Affiliations & Notes
  • O. S. Punjabi
    Ophthalmology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois
  • H.-S. Chung
    Ophthalmology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois
  • P. Cervantes
    Ophthalmology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois
  • M. Tsipursky
    Ophthalmology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois
  • M. K. Gill
    Ophthalmology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois
  • Footnotes
    Commercial Relationships  O.S. Punjabi, None; H.-S. Chung, None; P. Cervantes, None; M. Tsipursky, None; M.K. Gill, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 3289. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      O. S. Punjabi, H.-S. Chung, P. Cervantes, M. Tsipursky, M. K. Gill; Melanocytoma of the Optic Disk Associated With Visual Field Defect: Clinical Features and Imaging Using Spectral Domain Optical Coherence Tomography. Invest. Ophthalmol. Vis. Sci. 2009;50(13):3289.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose: : To study the clinical features and high definition optical coherence tomography (OCT) characteristics of melanocytoma of the optic disk with consistent visual field defects.

Methods: : Spectral Domain Optical Coherence Tomography (SDOCT) allows the acquisition of raster scans covering large regions of the retina at a very high speed (approximately 26000 A-scans/second). An observational study was performed in two patients diagnosed clinically with melanocytoma of the optic disk with consistent visual field defects using a commercially available (5 µm axial resolution) SDOCT system (CirrusTM, Carl Zeiss Meditec, Inc). SDOCT scans were obtained using two protocols- First, 5 high density B-scans (each having 4096 A-scans) were obtained in 0.5 seconds; and second, 128 B-scans (each having 512 A-scans) were obtained in 2.6 seconds, covering a 6x6mm area of the retina.

Results: : The fundoscopic appearance of melanocytoma is characterised by a deeply pigmented lesion with feathery edges, involving the optic disk and peripapillary choroid. Complications may include progressive slow growth, retinal vascular occlusions, choroidal neovascularization and rarely malignant transformation. OCT revealed an elevated lesion in the region of the optic disk having a highly reflective inner layer with posterior shadowing. SDOCT reconstructed fundus images obtained from these B-scans allowed accurate image registration. Regions of the melanocytoma that had deeper pigmentation had a thinner band of inner retinal reflectance and more posterior shadowing. In some regions, the highly reflective pigment band appeared to extend beyond the lamina cribrosa. Three-dimensional visualization of these lesions was possible following segmentation of the internal limiting membrane (ILM) and retinal pigment epithelium (RPE). These lesions appeared elevated in the peripapillary region and the retinal nerve-fiber layer was considerably thinner in the retina surrounding the tumor that corresponded to the altitudinal visual field defects in the hemisphere opposite to the tumor.

Conclusions: : SDOCT provided useful information about the morphology and extent of melanocytoma. Clinical exam, visual field and OCT may be useful in conjunction when monitoring patients with melanocytoma and consistent visual field defects.

Keywords: melanocytes • optic nerve • imaging/image analysis: clinical 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×