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Optic Atrophy

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Simply defined, this is a loss of function of the optic nerve with resulting gliosis and a decrease or loss of capillaries and axonal tissue within the nerve.  The type of optic atrophy depends on the pathogenetic factors involved; ascending damage from within the eye (glaucoma, optic neuritis, papilledema, and many primary lesions of the retina-choroid), descending from damage to the optic nerve or brain (trauma, hydrocephalus, neoplasm, demyelinating diseases), or due to congenital defect (Leber's optic atrophy). 

  Clinically, the atrophic disc appears white and pale diffusely.  Histologically, the myelin sheaths and axons degenerate, resulting in loss of substance of the optic nerve, causing expansion of the subarachnoid space (and causing the dura to appear redundant).  The pial septa thicken within the optic nerve due to proliferation of the glial, meningeal, and connective tissue elements.  Gliosis is also seen randomly within the nerve parenchyma.  Within the retina there is a corresponding loss of ganglion cells and nerve fiber layer. 

  Other clues such as loss of the inner nuclear layer (central retinal artery occulsion) or posterior bowing of the lamina cribrosa with cupping (glaucoma) may give clues to the origin of the atrophic process. 

 

Clinical #22087 High Power #22090
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Med. Power #22089
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John A. Moran Eye Center 50 North Medical Drive Salt Lake City UT 84132
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