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Parainfectious Optic Neuritis
Mostafa El Manhaly
Vitreoretinal Consultant
Msc/PhD/FRCSEd
Causes of Optic Neuritis
1. Idiopathic
2. Demylinating disorders
a) Multiple sclerosis
b) Devics disease
c) Schilder disease
d) acute disseminated encephalomyelitis
3. Infectious
sinus related (ethmoiditis) , cat scratch fever , syphilis , lyme disease, cryptococcal
meningitis
Parainfectious Optic Neuritis
Definition
Parainfectious optic neuritis is defined when optic nerve inflammation occurs after
presumably/confirmed systemic infectious disease, particularly of viral aetiology;
measles , mumps, chicken pox or following immunisation.
Differential diagnosis is extensive, particularly with other subtypes of optic
neuropathies.
To date, there is limited information about this entity in the literature.
Parainfectious Optic Neuritis
Pathogensis
The pathogenesis behind this disease is still uncertain but an autoimmune mechanism
is the most probable cause.
Parainfectious Optic Neuritis
Clinical picture
• Children are affected much more frequently than adults.
• Presentation is usually 1–3 weeks after a viral infection,
Acute
Severe
Bilateral
painless visual loss
• Bilateral papillitis is the rule;
occasionally there may be a neuroretinitis or the discs may be normal.
Parainfectious Optic Neuritis
• Children tend to manifest visual symptoms sooner after the antecedent
infection
• More often bilaterally
• In conjunction with ADEM (acute disseminated enchpalomyeilitis).
• The causative agent is isolated less frequently in children compared with
adults.
Parainfectious Optic Neuritis
Management and prognosis
The prognosis for spontaneous visual recovery is very good, and treatment is not
required in the majority of patients.
However, when visual loss is severe and bilateral or involves an only seeing eye,
intravenous steroids should be considered, with antiviral cover where appropriate.
Covid-19
Parainfectious Optic Neuritis
Covid-19 era: Postvaccination
Parainfectious Optic Neuritis
Covid-19: Myelin Oligodendrocyte Glycoprotein Antibody
MOG antibodies can circulate freely but do not exhibit a pathologic effect, unless they gain
access to the CNS through disruption of the blood– brain barrier, typically as a result of
inflammation or infection
Once access to the CNS is gained, pathology is mediated by T cells and complement-fixing
antibodies, leading to the varied clinical features associated with MOG antibody–mediated
CNS disease, including
• optic neuritis
• transverse myelitis
• encephalitis
• acute disseminated encephalomyelitis (ADEM)
Parainfectious Optic Neuritis
MOG associated optic neuritis post-Covid-19
27 male presented with Bilateral, subacute, sequential vision loss
Pain with eye movements preceded the vision symptoms in each eye.
Disc edema
OD HM and RAPD/ OS 20/250
He reported a few days of progressive dry cough before the onset of eye pain and vision loss.
He also endorsed numbness on the soles of his feet and neck discomfort with forward flexion
but denied shooting, electric-like pain.
SARSCoV- 2 polymerase chain reaction (PCR) testing was justified,
Lab: Quantiferon TB Gold Plus, rapid plasma reagin,
fluorescent treponemal antibody absorption test, anti-
nuclear antibody, anti-neutrophil cytoplasmic antibodies,
and aquaporin-4 (AQP4) and MOG-IgG cell-based
assays.
(Serum AQP4 antibodies were not detected; however,
MOG-IgG was highly positive at a titer of 1:1,000
1gm IV methylprednisolone was administered daily for 5
days, followed by an oral prednisone taper.
Visual acuity improved rapidly and incrementally to the
level of 20/50 in each eye by the time of discharge on
the seventh day after admission.
revealed avid, uniform enhancement and thickening
of both optic nerves extending from the globe to their
intracranial prechiasmal segments
To sum-up
• Parainfectious optic neuritis is commonly related to viral illnesses and post
immunizations.
• It occurs as a bilateral optic nerve affection and more common in children.
• Spontaneous visual recovery is warranted in the majority of cases.
• Covid-19 related optic neuritis with or without MOG antibodies are commonly
seen nowadays and may require systemic steroids in cases with severe
diminution of vision and disc edema.
Thank you

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Parainfectious optic neuritis

  • 1. Parainfectious Optic Neuritis Mostafa El Manhaly Vitreoretinal Consultant Msc/PhD/FRCSEd
  • 2. Causes of Optic Neuritis 1. Idiopathic 2. Demylinating disorders a) Multiple sclerosis b) Devics disease c) Schilder disease d) acute disseminated encephalomyelitis 3. Infectious sinus related (ethmoiditis) , cat scratch fever , syphilis , lyme disease, cryptococcal meningitis
  • 3. Parainfectious Optic Neuritis Definition Parainfectious optic neuritis is defined when optic nerve inflammation occurs after presumably/confirmed systemic infectious disease, particularly of viral aetiology; measles , mumps, chicken pox or following immunisation. Differential diagnosis is extensive, particularly with other subtypes of optic neuropathies. To date, there is limited information about this entity in the literature.
  • 4. Parainfectious Optic Neuritis Pathogensis The pathogenesis behind this disease is still uncertain but an autoimmune mechanism is the most probable cause.
  • 5. Parainfectious Optic Neuritis Clinical picture • Children are affected much more frequently than adults. • Presentation is usually 1–3 weeks after a viral infection, Acute Severe Bilateral painless visual loss • Bilateral papillitis is the rule; occasionally there may be a neuroretinitis or the discs may be normal.
  • 6. Parainfectious Optic Neuritis • Children tend to manifest visual symptoms sooner after the antecedent infection • More often bilaterally • In conjunction with ADEM (acute disseminated enchpalomyeilitis). • The causative agent is isolated less frequently in children compared with adults.
  • 7. Parainfectious Optic Neuritis Management and prognosis The prognosis for spontaneous visual recovery is very good, and treatment is not required in the majority of patients. However, when visual loss is severe and bilateral or involves an only seeing eye, intravenous steroids should be considered, with antiviral cover where appropriate.
  • 10. Parainfectious Optic Neuritis Covid-19: Myelin Oligodendrocyte Glycoprotein Antibody MOG antibodies can circulate freely but do not exhibit a pathologic effect, unless they gain access to the CNS through disruption of the blood– brain barrier, typically as a result of inflammation or infection Once access to the CNS is gained, pathology is mediated by T cells and complement-fixing antibodies, leading to the varied clinical features associated with MOG antibody–mediated CNS disease, including • optic neuritis • transverse myelitis • encephalitis • acute disseminated encephalomyelitis (ADEM)
  • 11. Parainfectious Optic Neuritis MOG associated optic neuritis post-Covid-19 27 male presented with Bilateral, subacute, sequential vision loss Pain with eye movements preceded the vision symptoms in each eye. Disc edema OD HM and RAPD/ OS 20/250 He reported a few days of progressive dry cough before the onset of eye pain and vision loss. He also endorsed numbness on the soles of his feet and neck discomfort with forward flexion but denied shooting, electric-like pain. SARSCoV- 2 polymerase chain reaction (PCR) testing was justified,
  • 12. Lab: Quantiferon TB Gold Plus, rapid plasma reagin, fluorescent treponemal antibody absorption test, anti- nuclear antibody, anti-neutrophil cytoplasmic antibodies, and aquaporin-4 (AQP4) and MOG-IgG cell-based assays. (Serum AQP4 antibodies were not detected; however, MOG-IgG was highly positive at a titer of 1:1,000 1gm IV methylprednisolone was administered daily for 5 days, followed by an oral prednisone taper. Visual acuity improved rapidly and incrementally to the level of 20/50 in each eye by the time of discharge on the seventh day after admission. revealed avid, uniform enhancement and thickening of both optic nerves extending from the globe to their intracranial prechiasmal segments
  • 13. To sum-up • Parainfectious optic neuritis is commonly related to viral illnesses and post immunizations. • It occurs as a bilateral optic nerve affection and more common in children. • Spontaneous visual recovery is warranted in the majority of cases. • Covid-19 related optic neuritis with or without MOG antibodies are commonly seen nowadays and may require systemic steroids in cases with severe diminution of vision and disc edema.

Editor's Notes

  1. Basically there are many cause for optic nerve inflammation, as idiopathic , demyelination with MS as the most common cause, infectious and post infection neuritis
  2. Still the pathogenesis is unclear, however it is thought to be of autoimmune origin
  3. In children, parainfectious optic neuritis occurs sooner , with bilateral affection more disseminated neurologically and the causative organism is not commonly isolated
  4. Typically the inflammation resolves spontaneously with good visual prognosis, however systemic steroid is indicated in severe visual loss
  5. To date, there was limited information about parainfectious optic neuritis in the literature.
  6. However , In the covid era, vaccination was claimed to be one of the causes of vision loss with one of the reports showing more than 50%of the patients had optic neuritis post vaccination
  7. Of the known causes of optic neuritis is the MOG ( myelin oligodendrocyte glycoprotein antibody)
  8. This is the first case reported in literature of
  9. All the lab studies were normal except for significant rise of the MOG antibody The patient received systemic steroids and he regained his vision.