Abstract
Optic nerve sheath dilatation or gadolinium-enhancement on magnetic resonance imaging in acute optic neuritis have been previously reported but have been thought to be rare occurrences. This study recruited 33 patients with acute unilateral optic neuritis. All had their optic nerves imaged with fat-saturated fast spin-echo (FSE) imaging, and 28 had imaging before and after triple-dose gadolinium-enhanced fat-saturated T1-weighted imaging. Follow-up imaging was performed on 20 patients (15 following gadolinium). A dilated subarachnoid space at the anterior end of the symptomatic optic nerve on FSE imaging was seen in 15/33 cases. In three of these cases, dilatation was visible on short-term follow-up. Optic nerve sheath enhancement was seen in 21/28 cases acutely: seven at the anterior end of the lesion only, five at the posterior end only and nine at both ends. Optic sheath enhancement was seen in 13 patients on follow-up. This study suggests that optic nerve sheath dilatation on FSE images and optic nerve sheath enhancement on triple-dose gadolinium-enhanced images are common findings in acute optic neuritis. Optic nerve sheath dilatation may be due to inflammation of the optic nerve, with its associated swelling, interrupting the communication between the subarachnoid space of the diseased optic nerve and the chiasmal cistern. Optic nerve sheath enhancement suggests that meningeal inflammation occurs in optic neuritis, in agreement with pathological studies of both optic neuritis and multiple sclerosis.
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References
Hickman SJ, Dalton CM, Miller DH, Plant GT (2002) Management of acute optic neuritis. Lancet 360:1953–1962
Optic Neuritis Study Group (1997) The 5-year risk of MS after optic neuritis: experience of the optic neuritis treatment trial. Neurology 49:1404–1413
Optic Neuritis Study Group (2003) High- and low-risk profiles for the development of multiple sclerosis within 10 years after optic neuritis: experience of the optic neuritis treatment trial. Arch Ophthalmol 121:944–949
Brex PA, Ciccarelli O, O’Riordan JI, Sailer M, Thompson AJ, Miller DH (2002) A longitudinal study of abnormalities on MRI and disability from multiple sclerosis. N Engl J Med 346:158–164
Gass A, Moseley IF, Barker GJ, Jones S, MacManus D, McDonald WI, Miller DH (1996) Lesion discrimination in optic neuritis using high-resolution fat-suppressed fast spin-echo MRI. Neuroradiology 38:317–321
Kupersmith MJ, Alban T, Zeiffer B, Lefton D (2002) Contrast-enhanced MRI in acute optic neuritis: relationship to visual performance. Brain 125:812–822
Hickman SJ, Toosy AT, Miszkiel KA, Jones SJ, Altmann DR, MacManus DG, Plant GT, Thompson AJ, Miller DH (2004) Visual recovery following acute optic neuritis: a clinical, electrophysiological and magnetic resonance imaging study. J Neurol 251:996–1005
Gass A, Barker GJ, Riordan-Eva P, MacManus D, Saunders M, Tofts PS, McDonald WI, Moseley IF, Miller DH (1996) MRI of the optic nerve in benign intracranial hypertension. Neuroradiology 38:769–773
Imamura Y, Mashima Y, Oshitari K, Oguchi Y, Momoshima S, Shiga H (1996) Detection of dilated subarachnoid space around the optic nerve in patients with papilloedema using T2 weighted fast spin echo imaging. J Neurol Neurosurg Psychiatry 60:108–109
Lindblom B, Norman D, Hoyt WF (1992) Perioptic cyst distal to optic nerve meningioma: MR demonstration. AJNR Am J Neuroradiol 13:1622–1624
Killer HE, Mironov A, Flammer J (2003) Optic neuritis with marked distension of the optic nerve sheath due to local fluid congestion. Br J Ophthalmol 87:249
Atlas SW, Galetta SL (1996) The orbit and visual system. In: Atlas SW (ed) MRI of the brain and spine, 2nd edn. Lippincott-Raven, Philadelphia, pp 1007–1092
Purvin V, Kawasaki A, Jacobson DM (2001) Optic perineuritis: clinical and radiographic features. Arch Ophthalmol 119:1299–1306
Carmody RF, Mafee MF, Goodwin JA, Small K, Haery C (1994) Orbital and optic pathway sarcoidosis: MR findings. AJNR Am J Neuroradiol 15:775–783
Kidd D, Burton B, Plant GT, Graham EM (2003) Chronic relapsing inflammatory optic neuropathy (CRION): a newly recognised steroid responsive syndrome seemingly distinct from sarcoidosis. Brain 126:276–284
Filippi M, Yousry T, Campi A, Kandziora C, Colombo B, Voltz R, Martinelli V, Spuler S, Bressi S, Scotti G, Comi G (1996) Comparison of triple dose versus standard dose gadolinium-DTPA for detection of MRI enhancing lesions in patients with MS. Neurology 46:379–384
Silver NC, Good CD, Barker GJ, MacManus DG, Thompson AJ, Moseley IF, McDonald WI, Miller DH (1997) Sensitivity of contrast enhanced MRI in multiple sclerosis: effects of gadolinium dose, magnetization transfer contrast and delayed imaging. Brain 120:1149–1161
Compston DA, Batchelor JR, Earl CJ, McDonald WI (1978) Factors influencing the risk of multiple sclerosis developing in patients with optic neuritis. Brain 101:495–511
Barkhof F, Valk J, Hommes OR, Scheltens P (1992) Meningeal Gd-DTPA enhancement in multiple sclerosis. AJNR Am J Neuroradiol 13:397–400
Guseo A, Jellinger A (1975) The significance of perivascular infiltrations in multiple sclerosis. J Neurol 211:51–60
Ikeda H, Tansey EM (1986) Virus-induced demyelination in the optic nerve of the mouse, I: morphological and axonal transport studies. In: Hess RF, Plant GT (eds) Optic neuritis. Cambridge University Press, Cambridge, pp 255–270
Lightman S, McDonald WI, Bird AC, Francis DA, Hoskins A, Batchelor JR, Halliday AM (1987) Retinal venous sheathing in optic neuritis: its significance for the pathogenesis of multiple sclerosis. Brain 110:405–414
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S.J.H. is supported by The Wellcome Trust. The NMR Research Unit is supported by the Multiple Sclerosis Society of Great Britain and Northern Ireland.
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Hickman, S.J., Miszkiel, K.A., Plant, G.T. et al. The optic nerve sheath on MRI in acute optic neuritis. Neuroradiology 47, 51–55 (2005). https://doi.org/10.1007/s00234-004-1308-x
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DOI: https://doi.org/10.1007/s00234-004-1308-x