Optic perineuritis (OPN) is a rare inflammatory disorder in which the inflammation is confined to optic nerve sheath. It can be idiopathic or secondary to underlying systemic autoimmune disorder. It usually presents with unilateral progressive diminution of vision with pain on eye movements and optic disc oedema. Hence, clinically OPN mimics optic neuritis resulting in delayed diagnosis and suboptimal treatment. In contrast to optic neuritis, patients with OPN are usually of older age group and more likely show sparing of central vision. MRI is an important tool for diagnosis of OPN apart from optic nerve sheath biopsy. Perineural enhancement on MRI is diagnostic of OPN. Oral corticosteroid therapy gives dramatic and rapid improvement in signs and symptoms. Rapid tapering of steroids increases the risk of relapse. Overall, prognosis of OPN is generally good if adequate treatment is given timely.
- treatment medical
- optic nerve
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Optic perineuritis (OPN), also known as perioptic neuritis, is a rare form of orbital inflammatory disease in which the optic nerve sheath is inflamed, resulting in marked thickening due to non-specific fibrosis1 as opposed to the inflammation of the optic nerve axons in optic neuritis (ON). It is usually isolated and idiopathic in nature (primary OPN) but can occur secondary to infections and autoimmune diseases (secondary OPN) such as Antineutrophil Cytoplasmic antibodies (ANCA)-associated vasculitis,2 sarcoidosis,3 4 syphilis5 6 and Crohn’s disease.7 First described by Edmunds and Lawford,8 OPN usually presents with pain, disc oedema and various features of optic nerve dysfunction. Radiologically, OPN may simulate optic nerve sheath meningioma,9 but clinically, it more often mimics acute demyelinating ON, thus resulting in late diagnosis and treatment. It is important to distinguish between these two entities due to differences in their treatment and prognosis.
In the past, OPN was originally described as an optic neuropathy with optic disc oedema but without optic nerve dysfunction in the setting of normal intracranial pressure.10 This often occurs with syphilis infection of the optic nerve.11 However, with the emergence of modern neuroimaging techniques (MRI) that enabled imaging of the nerve sheath, the clinical and radiological features of OPN were revised.
Method of literature search
We conducted a systematic review using the Cochrane methodology and reported the findings according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses. CINAHL, EMBASE, Cochrane Library, MEDLINE, OTSeeker, PEDro and PsycINFO databases were searched using the terms ‘optic neuritis’, ‘optic perineuritis’, ‘demyelinating’ and ‘multiple sclerosis’. Related definitions and descriptions were extracted. Two independent reviewers determined whether the studies met inclusion the inclusion criteria: reviews or randomised controlled trials; categorised interventions based on the name, core components and diagnostic populations; rated the quality of evidence and determined the strengths of recommendations using the GRADE criteria; and made recommendations using the evidence alert traffic light system.
Edmunds and Lawford described two forms of OPN: an exudative form, in which there is localised non-suppurative pachymeningitis; 9 12 and a purulent form, in which the leptomeningitis extends to involve the subarachnoid space around the optic nerve. In such cases, optic nerve function is considered to be normal as the inflammatory infiltrate is loosely organised around the optic nerve.
The common pathological reaction in OPN involves marked inflammatory thickening of the optic nerve sheath due to non-specific fibrosis.9 Visual loss in OPN has been attributed to secondary ischaemic infarction of the optic nerve due to circumferential compression of the optic nerve periphery by the mass of the thickened optic nerve sheath.13 Various stages of predominantly lymphocytic infiltration of the sheath and adjacent optic nerve parenchyma are usually present in biopsy specimens. Few authors have reported the presence of foci having degenerating (necrobiotic) collagen and vasculitic changes in the optic nerve sheath in cases of chronic inflammation.13 In their study, Dutton and Anderson showed the presence of granulomatous inflammation in the optic nerve sheath of one out of four patients.9 In chronic cases, the perivascular lymphocytic infiltration of the small optic nerve vessels (vascultits) has also been identified in a few patients.14 15 Some cases have immune-mediated inflammation within the nerve sheath along with a few axons of optic nerve being affected. The degree and location of the optic nerve sheath inflammation defines the range of signs and symptoms seen in the disease. However, most cases are idiopathic.
OPN is usually seen in older patients as compared with ON, which is more prevalent in the middle age group. Purvin et al reported a case series in 2001 involving 14 patients with OPN, where the mean age of presentation was 41 years.1 OPN is more common in women. Unlike ON, OPN is not associated with multiple sclerosis.
Most cases of OPN are idiopathic, isolated and include primary OPN. However, many cases have been reported to occur secondary to systemic disorders such as Myelin Oligodendrocyte protein (MOG) antibody-associated demyelinating disease mimicking typical multiple sclerosis, sarcoidosis,3 4 giant cell arteritis (GCA),16 tuberculosis,17 herpes simplex virus,18 herpes zoster virus,17 leukaemia,19 syphilis,5 6 wegener’s granulomatosis2 primary or metastatic malignancy,20 Crohn’s disease,7 IgG4-related disease20 and neuroretinitis.21 Lai et al stated that majority of patients with OPN were diagnosed with Behcet’s disease, suggesting that OPN might be a precursor to other autoimmune diseases.21 22
Patients with OPN often present with acute vision loss progressing over several weeks and eye pain exacerbated with eye movement similar to ON, but the pain is more severe or longer lasting. Visual loss can range from none to severe, described by patients as blurring of vision, dimming, splotches or ‘spots’ in vision.1 On fundus examination, OPN patients have disc oedema in the affected eye. Usually, there is sparing of central vision with defects in the visual field such as paracentral scotomas, arcuate defects, centrocaecal scotomas, peripheral islands and altitudinal defects, and rarely, central scotomas. In addition, patients have signs and symptoms of optic nerve dysfunction, such as the possible presence of an relative afferent pupillary defect dyschromatopsia and poor contrast sensitivity. Unlike isolated ON, OPN may present with orbital signs and symptoms such as ophthalmoplegia, ptosis and exophthalmos,17 and rarely with intraocular lesions such as retinal necrosis, scleritis and episcleritis.
OPN is often clinically difficult to differentiate from ON and other inflammatory conditions because of their similar signs and symptoms. However, it is important to differentiate between the two entities due to their different therapeutic and prognostic implications. Patients with ON are at increased risk of developing multiple sclerosis and need to be counselled accordingly, whereas OPN is not associated with a risk for developing multiple sclerosis but is associated with recurrent visual loss. In addition, the treatment recommended for OPN (oral glucocorticoids) is contraindicated in ON because of the chance of recurrence of ON with oral steroids. The key differences between ON and OPN are shown in table 1.
OPN is diagnosed on the basis of clinical and radiographic findings.1 Ideally, to detect the classic perineural enhancement optic nerve sheath in OPN, a fat-suppressed, Gadolinium-enhanced T1 weighted MRI of the orbits should be performed.9 Unlike ON, wherein optic nerve enhancement is seen on MRI, the characteristic finding in OPN is the contrast enhancement of the optic nerve sheath with sparing of the optic nerve. This perioptic enhancement in OPN appears as ‘Tram Tracks’ in the axial view and as a ‘Doughnut’ in the coronal view.1 However, this tram track sign is not specific to OPN as it can also be seen in other inflammatory or neoplastic diseases affecting the optic nerve sheath, such as optic nerve sheath meningioma, sarcoidosis, lymphoma, leukaemia, orbital pseudotumor, perioptic haemorrhage and metastasis.23 Optic nerve sheath meningioma can be differentiated on the basis of calcifications, which can be seen using CT if the diagnosis is unclear.3 It is important to not confuse the tram track sign with normal enhancement of the dural sheath due to its rich vascular supply.23 Other findings that can be seen in OPN are the subtle enhancement of the sclera and extraocular muscles, which may present as a mild motility limitation leading to diplopia and the streaky enhancement of orbital fat.1 A CT scan can also be done to examine these features, but its spatial resolution cannot sufficiently differentiate intraneural enhancement from perineural enhancement.1 During the pre-MRI era, OPN was misdiagnosed as ‘atypical corticosteroid-responsive ON’. (table 2)
The diagnosis of OPN can be confirmed with optic nerve biopsy, but it is usually not routinely indicated.17 It is usually useful in patients showing no response to corticosteroids and in those with no defining underlying aetiology for OPN.17 Optic nerve sheath inflammation is evidenced by predominantly lymphocytic infiltration and/or detection of perineural fibrous tissue.1 9
Apart from neuroimaging, other laboratory tests can be performed in cases where no clear underlying aetiology can be detected. These include serological tests for syphilis24; serum ACE for sarcoidosis25; Mantoux test and chest X-ray for tuberculosis15; ANCA, IgG4, erythrocyte sedimentation rate for GCA,26 granulomatosis with polyangitis2 27 and Behcet’s disease22 and lumbar puncture CSF analysis to rule out central nervous system malignancy and infection. Thus, evaluation of patients with suspected infectious optic neuropathy may include testing complete blood count; erythrocyte sedimentation rate; C reactive protein; serological testing; blood cultures; PCR or antibody assessment of aqueous humour, vitreous, serum or cerebrospinal fluid; a tuberculin skin test and/or quantification; tomodensitometry and MRI. Since serum ACE has low yield for the detection of neurosarcoidosis, patient evaluation should include a chest CT or Positron emission tomography (PET)-CT scan of the body. Similarly, the evaluation for tuberculosis would include an Interferon-Gamma Release Assay (IGRA) test in addition to chest imaging.
Orbital inflammatory syndromes (idiopathic, sarcoidosis, granulomatous).
Neoplasms (optic nerve sheath meningioma, leukaemia, lymphoma).
Infectious causes (tuberculosis, syphilis).
Posterior scleritis, secondary disc oedema associated with uveitis.
MOG antibody-associated demyelinating disease mimicking typical multiple sclerosis.
The main treatment for OPN is corticosteroid therapy, which causes rapid and dramatic improvement in signs and symptoms typically within hours or within a day. However, recurrence has been reported with a short course of treatment, thus requiring a longer course of treatment with very slow tapering of the dose. The dosage depends on the frequency and rate of recurrence.28 Few cases have been reported that showed no improvement in vision even with corticosteroid therapy.22 This was attributed to chronic inflammatory infiltration along with fibrous tissue deposition in the dural sheath causing compressive optic neuropathy and ischaemic infarction.31 In a case study conducted by Purvin et al, indomethacin was used instead of steroids and was able to successfully treat two patients.1 Although steroids are the mainstay of OPN therapy, radiation therapy and immunosuppressants such as azathioprine have also been reported to be successful for refractory cases.17
OPN is not self-limiting; that is, it does not resolve without treatment. Corticosteroid therapy improves final visual outcomes in OPN unlike in ON, while treatment with intravenous steroids only speeds up the visual recovery but does not affect final visual outcomes.1 Additionally, the dose and route of steroid administration differ. The preferred mode of treatment for OPN is oral and requires a higher dose of steroids (80 mg/day), whereas in ON, the preferred mode is intravenous since there is a higher risk of recurrence reported with the use of oral steroids in ON. A short course of treatment used in ON (approximately 2 weeks) is generally not long enough to achieve lasting remission in OPN.1 The relapse of symptoms after cessation of therapy is more common in OPN. Hence, if a patient treated for ON shows relapse after therapy, the possibility of OPN should be considered.
OPN usually has a relatively good visual prognosis. Unlike ON, OPN is not associated with multiple sclerosis. The prognosis is influenced by the gap between the onset of visual loss and the initiation of steroid therapy. Another factor that influences prognosis is the frequency of recurrent attacks. OPN secondary to Behcet’s disease has been reported to have a poor prognosis.22 A long duration of treatment with high-dose steroids can lead to complications in OPN.
OPN is a rare heterogeneous disease presenting with inflammation restricted to the optic nerve sheath rather than being more extensive within the orbit, as in other orbital inflammatory diseases.3 An older patient presenting with the classic triad of pain, optic neuropathy (relative afferent pupillary defect, loss of colour vision and contrast sensitivity), and optic disc swelling should be examined for possible OPN, especially if central vision is spared. A full history, as well as an ocular and systemic examination should be performed to rule out any underlying systemic disease. A fat-suppressed, gadolinium-enhanced T1-weighted MRI of the brain and orbit is of utmost importance for the diagnosis of OPN. It is useful for differentiating OPN from ON, other orbital inflammatory diseases and neoplasms. Optic nerve sheath biopsy is indicated in refractory cases and if the underlying aetiology is not known. Once OPN is diagnosed, high-dose oral steroids are administered for a period of months. Poor prognosis has been reported in cases with delayed initiation of treatment. Hence, early diagnosis and treatment of OPN are important.
Contributors All the authors were involved in the concept and design of the study, data acquisition, data analysis and interpretation, drafting manuscript, technical support and final review of the manuscript.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.