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Abstract

Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory disorder of the central nervous system (CNS) mostly manifesting as optic neuritis and/or myelitis, which are frequently recurrent/bilateral or longitudinally extensive, respectively. As the autoantibody to aquaporin-4 (AQP4-Ab) can mediate the pathogenesis of NMOSD, testing for the AQP4-Ab in serum of patients can play a crucial role in diagnosing NMOSD. Nevertheless, the differential diagnosis of NMOSD in clinical practice is often challenging despite the phenotypical and serological characteristics of the disease because: (1) diverse diseases with autoimmune, vascular, infectious, or neoplastic etiologies can mimic these phenotypes of NMOSD; (2) patients with NMOSD may only have limited clinical manifestations, especially in their early disease stages; (3) test results for AQP4-Ab can be affected by several factors such as assay methods, serologic status, disease stages, or types of treatment; (4) some patients with NMOSD do not have AQP4-Ab; and (5) test results for the AQP4-Ab may not be readily available for the acute management of patients. Despite some similarity in their phenotypes, these NMOSD and NMOSD-mimics are distinct from each other in their pathogenesis, prognosis, and most importantly treatment. Understanding the detailed clinical, serological, radiological, and prognostic differences of these diseases will improve the proper management as well as diagnosis of patients.

Keywords

aquaporin-4 antibody Devic’s disease differential diagnosis longitudinally extensive transverse myelitis multiple sclerosis myelin oligodendrocyte glycoprotein antibody neuromyelitis optica spectrum disorders optic neuritis

Introduction

Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory disease of the central nervous system (CNS), mostly involving the optic nerve and the spinal cord.¹ Though it is a rare disease, a recent epidemiologic study estimated its prevalence to be as high as 10 per 100,000 in an Afro-Caribbean population.² NMOSD characteristically shows a high female predominance from 3:1 to 9:1,^3–5 is accompanied by severe disruption of the blood–brain barrier during attacks,⁶ mostly has a disease-specific autoantibody to aquaporin-4 (AQP4-Ab),⁷ and frequently manifests as severe bilateral/recurrent optic neuritis or severe longitudinally extensive transverse myelitis (LETM).⁸ However, diverse diseases such as multiple sclerosis (MS), other inflammatory diseases,⁹ malignancy, infection, or vascular disease can mimic NMOSD by either involving optic nerves and/or spinal cords, manifesting bilateral optic neuritis or LETM,¹⁰ showing brain lesions resembling those of NMOSD, or even having false-positive AQP4-Ab assay results.^11–13 Moreover, some of the NMOSD can manifest as atypical or milder forms¹⁴ or test negative in the AQP4-Ab assay,^1,15 thereby complicating the diagnosis. In this review we will cover the history of the diagnostic criteria of NMOSD, the advantage and pitfalls of the AQP4-Ab assays, and diverse diseases that can mimic NMOSD, including the key features that can distinguish them from NMOSD.

Diagnosis of NMOSD

Neuromyelitis optica (NMO) was first reported by Dr. Eugène Devic in the late 19th century as a monophasic disease characterized by both severe bilateral optic neuritis and transverse myelitis (TM).¹⁶ In addition to the classic concept of the 19th century, recent studies have revealed that NMO is often relapsing rather than monophasic,¹⁷ frequently associated with a disease-specific autoantibody against AQP4-Ab,¹⁸ and can also involve the brain as well as the optic nerve and spinal cord.¹⁹

With deeper understanding of NMO, the diagnostic criteria of NMO also evolved from the version in 1999,¹⁷ through the revised one in 2006,²⁰ and finally to the first international consensus criteria in 2015.¹ The new criteria have adopted the broader term of NMOSD⁸ to include patients with limited manifestations. Moreover, they have stratified NMOSD into two types: NMOSD with AQP4-IgG (NMOSD-AQP4); and NMOSD without AQP4-IgG or with unknown AQP4-IgG status. According to the new diagnostic criteria, NMOSD-AQP4 refers to patients (1) who have at least one core clinical characteristics of NMOSD in either optic nerve, spinal cord, dorsal medullar, brainstem, diencephalon, or cerebrum; (2) who were tested positive for AQP4-IgG; and (3) in whom alternative diagnoses are excluded.¹

The AQP4-Ab assay: implications and caveats

The AQP4-Ab is a disease-specific autoantibody to NMOSD. If tested by proper assay methods this autoantibody is rarely found in patients having other neurological diseases nor in healthy subjects.²¹ Therefore, the presence of serum AQP4-Ab is a highly specific diagnostic test of NMOSD as set out in the recent international consensus criteria.¹ Moreover, the presence of AQP4-Ab in patients with NMOSD can predict their long-term prognosis as well as therapeutic response.¹⁴

Currently, diverse methods such as indirect immunofluorescence (IIF), enzyme-linked immunosorbent assay (ELISA), cell-based assay (CBA), and flow cytometry assay (FACS-assay) are available for detecting AQP4-Ab. Among these, the CBAs are strongly recommended according to the 2015 international consensus diagnostic criteria.¹ CBA can be performed using either live cells expressing human M23-AQP4 (live-CBA) or a commercial kit coated with pre-fixed cells expressing human M1-AQP4 (fixed-CBA). The fixed-CBA is currently widely used as it is ready-to-use and has relatively good accuracy. The live-CBA seems to have higher accuracy than the fixed-CBA, but demands a high level of technical expertise and is time-consuming, which limits its use to some specialized centers.^12,22 Therefore, if AQP4-Ab assay results, performed with the fixed-CBA results, were distinct from the clinical and/or radiological manifestations of patients, it would be reasonable to re-test their samples with the live-CBA. Some studies reported that the FACS-assay, using free-floating live cells expressing human AQP4, yielded a higher sensitivity than the fixed-CBA²³ or even the live-CBA.^22,24 The FACS-assay could also be advantageous in that it can yield quantitative results and a cut-off discriminator. Nevertheless, as the accuracy of the FACS-assay varied greatly according to the methodological details and experience of the examiners,¹² further studies for the optimal protocol of FACS-assay are needed. The IIF was the first assay to identify NMO-IgG,⁷ and can be useful as a screening tool for diverse antibodies against the CNS antigens, including AQP4-Ab, at a relatively low cost.²⁵ The ELISA may easily quantify the titer of AQP4-Ab²⁶ but has a relatively low accuracy.^12,22,24

Other than the assay methods, various clinical and serological situations can lower the accuracy of AQP4-Ab assay (Table 1).

Table 1.

Conditions that may affect the diagnostic accuracy of the AQP4-Ab assay.

• Sera sampled immediately after or during plasmapheresis/high-dose corticosteroid often lowers the titers of AQP4-Ab.²⁷

• Sera sampled during B-cell-depleting treatment (e.g. rituximab) or during remission stage may have lower titers of AQP4-Ab and be tested false-negative.²²

• Sera with polyclonal B-cell activation can cause non-specific binding to cells and may give false-positive results.²¹

• Pre-fixation of the AQP4-expressing cells and/or using an M1-AQP4 isoform can interfere with the formation of the orthogonal array of particles of AQP4, and might give false-negative results.^28,29

• Sera with lower titers of AQP4-Ab may be tested negative in a fixed-CBA.²³

• Sera with highly active AQP4-Ab can destroy AQP4-expressing cells, and thereby may mask the binding of the AQP4-Ab in assays using live cells (either live-CBA or FACS-assay).¹³

• Recently a case report showed that natalizumab can directly interact with the AQP4-expressing cells, and thereby might cause false-positive AQP4-Ab assay results in patients being treated with natalizumab.³⁰

Differential diagnosis of NMOSD

According to the 2015 international panel criteria, the presence of AQP4-Ab in the sera of patients is central in diagnosing NMOSD-AQP4. Nevertheless, clinical and radiological differential diagnoses of NMOSD-AQP4 remains important for the following reasons: (1) in clinical practice, the AQP4-Ab assay may not be performed for all the patients with inflammatory disease of the CNS, or not be readily available everywhere. Rather, clinicians need to identify patients with probable NMOSD-AQP4, in whom the AQP4-Ab assay needs to be performed; (2) the test result for AQP4-Ab could be affected by such factors as types of assay and clinical and serological situations; (3) many diseases, including inflammatory, infectious, or neoplastic conditions, can involve the CNS and mimic the clinical and radiological phenotypes of NMOSD-AQP4; and lastly (4) some patients with NMOSD do not have AQP4-Ab.¹

Multiple sclerosis

Both MS and NMO are inflammatory diseases of the CNS with relapsing courses, especially in their early disease stages.^31,32 As these two diseases share some phenotypic features, there have been long debates on whether these two diseases are fundamentally different. However, since the discovery of the disease-specific autoantibody to NMO (AQP4-Ab), subsequent studies have confirmed that these two diseases have distinct features in their epidemiology, serology, pathology, response to treatment, and prognosis. These characteristics provide important clues in differentiating the two diseases, as summarized in Table 2. Differential diagnosis of MS from NMOSD is critically important because disease-modifying treatment for MS, such as interferon-β,^33,34 fingolimod,³⁵ natalizumab,^36,37 and alemtuzumab,³⁸ are inefficacious in or may aggravate NMOSD.³⁹

Table 2.

Distinctive characteristics of MS from those of NMOSD.

		MS	NMOSD	References
Epidemiology
Prevalence, per 100,000⁵ people	Denmark	154.5 nationwide	4.4 in southern Denmark	Asgari et al.,⁴⁰ Bentzen et al.⁴¹
	US	177 in Olmsted county	3.9 in Olmsted county	Mayr et al.⁴²
	Martinique, France		10 in Martinique	Flanagan et al.²
	UK	203.4 nationwide	1.96 in southeast Wales	Cossburn et al.,⁴³ Mikaeloff et al.⁴⁴
	Japan	10 nationwide	3.65 nationwide	Ochi and Fujihara,⁴⁵ Miyamoto⁴⁶
F:M ratio		Moderate female predominance	High female predominance (9:1–3:1).	Kim et al.,^5,47 Koch-Henriksen and Sorensen⁴⁸
Age of onset		Median of 29 years, uncommon in children and >50 years	Mean of 40–45 years, with wide distribution from young children to elderly	Kitley et al.,⁴ Kim et al.,⁵ Wingerchuk and Lucchinetti⁴⁹
Symptoms and signs
Optic neuritis	Visual field defect other than cecocentral scotoma (per se, complete blindness, altitudinal hemianopsia, etc.)	Uncommon	Relatively common (up to 25%)	Nakajima et al.⁵⁰
	Severe visual loss (bilaterally ⩽0.1) in the chronic stage	Uncommon (4.2% in 11 years of disease onset)	Common (50% in 10 years of disease onset)	Merle et al.⁵¹
Myelitis	Severe myelitis causing complete paraplegia	Rare	Relatively common (30–70% at first attack)	Wingerchuk⁵²
	Painful tonic spasm associated with myelitis	Rare	Relatively common (up to 25%)	Kim et al.⁵³
Brain	Intractable hiccup and nausea (associated with area postrema lesions)	Rare	Relatively common (12–17%)	Apiwattanakul et al.,⁵⁴ Misu et al.⁵⁵
MRI findings
Spinal cord	Longitudinally extensive spinal lesion extending three or more vertebral segments	Adult: rare (<5%)Pediatric: relatively uncommon (14%)	Adult: very common (up to 94%)Pediatric: very common (up to 100%)	Wingerchuk et al.,²⁰ Banwell et al.⁵⁶
	Location of spinal lesions on axial image	Asymmetrical and peripheral, often posterior involvement	Central gray matter involvement	Kim et al.⁵⁷
	Bright spotty lesions, defined as very hyperintense spotty lesions on axial T2WI	Rare (3%)	Common (54%)	Yonezu et al.⁵⁸
Brain	Multiple patchy enhancement with blurred margin in adjacent regions (cloud-like enhancement)	Uncommon (8%)	Common (90%)	Ito et al.⁵⁹
	Pattern of callosal lesions	Small, isolated, and non-edematous	Can be large and edematous	Nakamura et al.⁶⁰
	Lesions perpendicular to a lateral ventricle (Dawson fingers)	Common	Rare	Matthews et al.⁶¹
	Lesions adjacent to lateral ventricle and the inferior temporal lobe	Common	Rare	Matthews et al.⁶¹
	Large and confluent white matter lesions, sometimes resembling pattern of PRES	Very rare	Sometimes	Kim et al.,⁶² Magana et al.,⁶³ Pittock et al.⁶⁴
	Cortical or juxtacortical lesions	Common	Rare	Matthews et al., Calabrese et al.⁶⁵
Optic nerve	Optic chiasmal involvement	Rare	Relatively common (25–75%)	Storoni et al.,⁶⁶ Lim et al.,⁶⁷ Khanna et al.⁶⁸
Pattern of CNS atrophy
		More severe atrophy of the brain	More severe atrophy of the spinal cord	Liu et al.⁶⁹
Serology
	Serum AQP4-Ab	Not present	Can be present in average of 72% of NMO by in-house cell-based assay (results vary greatly according to the types of assay methods and definition of the sample populations)	Jarius and Wildemann²¹
Cerebrospinal fluid study
	Pleocytosis	Mild to moderate	Can be severe (up to 1,000/mm³)	Kim et al.,⁶ Wingerchuk et al.¹⁷
	Oligoclonal bands	Present in most patients (up to 97% with repeated test); rarely disappear in follow-up sampling	Can be present in some patients (33–43%); mostly disappear in follow-up sampling	Wingerchuk et al.,¹⁷ Bergamaschi et al.⁷⁰
	Polyspecific antiviral humoral immune response (e.g. against measles, rubella, varicella)	Common (88%)	Rare (5%)	Jarius et al.⁷¹
Optical coherence tomography
	Retinal nerve fiber layer thickness reduction	Mostly in temporal quadrant	Mostly in superior/inferior quadrant	Schneider et al.,⁷² Bennett et al. ⁷³
Pathology
	AQP4 immunoreactivity	Relatively preserved	Lost in the early stage	Lucchinetti et al.,⁷⁴ Misu et al.,⁷⁵ Roemer et al.,⁷⁶ Misu et al.⁷⁷
	GFAP immunoreactivity	Relatively preserved	Can be lost in the early stage;some lesions can show clasmatodendrosis
	Perivascular deposition of the immunoglobulin and complement	Rare	Common
Prognosis
	Secondary progressive course	Common	Proposed to be uncommon (2%; data were based on the 2006 NMO criteria, data based on 2015 criteria have not been evaluated yet)	Wingerchuk et al.³²
	Rate of disability progression	Relatively slow (median duration of 23.1 years from onset to EDSS 6 reported in earlier study, recent studies show milder disease courses)	Can be fast (median 12 years to EDSS 6)	Kim et al.,⁴⁷ Confavreux et al.,⁷⁸ Cree et al.^79,80
	Mortality	Low (life expectancy is reduced by 7–14 years compared with the general, healthy population)	Can be high (the five-year survival can be as low as 68%, as identified in an earlier study)	Wingerchuk et al.,¹⁷ Scalfari et al.⁸¹

AQP4, aquaporin-4; AQP4-Ab, autoantibody to aquaporin-4; EDSS, expanded disability status scale; GFAP, glial fibrillary acidic protein; MS, multiple sclerosis; NMOSD, neuromyelitis optica spectrum disorder; PRES, posterior reversible encephalopathy syndrome.

Acute disseminated encephalomyelitis

Acute disseminated encephalomyelitis (ADEM) is a rare inflammatory demyelinating disorder of the CNS. It typically causes multiple simultaneous or consecutive lesions in the CNS, thereby manifesting as polyfocal neurologic symptoms including encephalopathy, motor and sensory symptoms originating from the brain, optic neuritis, and/or TM (Figure 1).^82,83 Though ADEM is often monophasic, recent studies reported that relapses can occur in 10–18% of cases.^44,84,85 ADEM can manifest as LETM, bilateral multiple cerebral lesions of the white matter,⁸⁶ bilateral optic neuritis,⁸⁷ or deep gray matter lesions,⁸⁸ all of which can be seen in NMOSD.¹ Moreover, a considerable number of patients diagnosed with ADEM in clinical practice did not meet the current diagnostic criteria for ADEM,⁸⁴ highlighting the difficulties in defining ADEM.

Figure 1.

Polyfocal manifestation of acute disseminated encephalomyelitis. A = fat-suppressed T1-weighted image with gadolinium enhancement; B = T2-weighted image; C, D, E, and F = fluid-attenuated inversion recovery (FLAIR).

ADEM differs from NMOSD in that it has no AQP4-Ab, less or no female predominance, more polyfocal neurologic symptoms at onset, typically a monophasic disease course, and is relatively more common among pediatric patients than the latter.^83,84 Moreover, the major symptom of ADEM is encephalopathy that can manifest as either alteration in consciousness or behavioral change;⁸³ by contrast, the major symptom of NMOSD is either optic neuritis or myelitis, and only a minor proportion (about 8%) of patients with NMOSD have symptomatic cerebral syndrome at disease onset.⁸⁹

Another characteristic feature of ADEM distinguishing it from NMOSD is that most patients with ADEM experience preceding infection (up to 61%) or vaccination (up to 4%) within 4 weeks before the onset of neurologic deterioration.⁸⁴ A recent study on the brain lesion distribution in ADEM and NMOSD reported that brain lesions in the putamen favor the diagnosis of ADEM, whereas lesions in the hypothalamus favor the diagnosis of NMOSD.⁸⁸ Though patients with ADEM have initial severe neurologic impairment and show polyfocal/diffuse MRI lesions, most of their symptoms and MRI lesions recover over the long term (Figure 1).⁸⁵ Classically, uniform enhancement of all MRI lesions has been considered to be a feature that favors diagnosis of ADEM, since all lesions in ADEM can be theoretically in their same disease stage.⁹⁰ Nevertheless, care should be taken in applying this features to the diagnosis of ADEM in clinical practice because enhancing MRI lesions can be found in a limited number of patients with ADEM (30–66%);^82,85 moreover, some patients with ADEM may experience multiphasic disease courses⁸³ with lesions having diverse disease stages.

Interestingly, the original concept of NMO, proposed by Dr. Eugine Devic in 1894, more closely resembled the current concept of ADEM^82,83 than that of NMOSD,¹ because the original concept of NMO suggested a monophasic disease course and polyfocal manifestation of optic neuritis and TM occurring at the same time or in quick succession.¹⁶ Even now, it seems that the current concept of ADEM still contains some overlaps with those of MS and NMOSD. According to the recent criteria and expert opinion for pediatric ADEM, patients with ADEM can be re-diagnosed as having either MS or NMOSD according to the number/types of relapses or test result for AQP4-Ab, respectively.^83,91 These overlaps in phenotypes should be considered especially in diagnosing pediatric ADEM patients, since a relatively higher portion (up to 9%) of pediatric NMOSD-AQP4 cases can manifest as symptoms of encephalopathy mimicking ADEM.⁹²

Idiopathic acute transverse myelitis

Acute transverse myelitis (ATM) refers to a heterogeneous group of inflammatory spinal cord disorders, resulting in motor, sensory, and/or bowel and bladder dysfunction. ATM can be a symptom of either MS, NMO, systemic connective tissue disease, infectious disease, radiation, or malignancy. However, despite extensive diagnostic workup, etiologies in some cases of ATM are unknown (idiopathic ATM, iATM). According to the definition of the Transverse Myelitis Consortium Working Group (TMCWG), iATM should have symptoms arising from the spinal cord, bilateral signs and/or symptoms, a clear sensory level, no extra-axial compression of the spinal cord, evidence of inflammation within the spinal cord, and progression to nadir in 4 h to ~21 days. Moreover, iATM should not have evidence of aforementioned other etiologies that cause secondary inflammation of the spinal cord.⁹³

Although the presence of LETM is an important feature in differentiating NMOSD from MS,²⁰ LETM can be a feature of other diseases and, conversely, short TM can occur in NMOSD-AQP4 patients.^94,95 Studies in Asians and individuals of European ancestry showed that positivity of AQP4-Ab among inflammatory disease patients with LETM was as low as 18% and 53%, respectively,^14,96 implying that diverse diseases, including iATM, can manifest as LETM.

A study in Europe showed that about 80% of patients with a first episode of ATM converted to MS after a mean follow-up period of 6.2 years.⁹⁷ Meanwhile, the majority of ATM in the Asian cohort did not convert to MS after a mean follow-up period of 5.3 years.⁹⁸ Therefore it seems that the prognosis and clinical significance of isolated ATM may depend on the ethnic background and the prevalence of MS among the population.

Notably, contrary to the definition of iATM by TMCWG, which suggested a time to nadir in 4 hours to ~21 days in iATM, myelopathy with a progressive course over months has also been reported in NMOSD,^99,100 which could be attributable to successive or clustering of individual relapses of myelitis in NMOSD.¹⁷

Among patients with ATM, painful tonic spasms, defined as a paroxysmal episode of intense pain that accompanies tonic posturing of the limbs, have been reported to be more common in NMOSD than in iATM groups (25% versus 2%, respectively).⁵³ Female gender, recurrent disease course, higher expanded disability status scale (EDSS) at the nadir of acute attack, and poor response to acute steroid treatment were also associated with the presence of AQP4-Ab among patients with isolated LETM, implying these factors can be an important clue in differentiating LETM of NMOSD from idiopathic LETM.¹⁴

Idiopathic optic neuritis

Optic neuritis is probably the most common cause of unilateral visual loss among young adults. The general features of optic neuritis includes reduction in visual acuity, field defects relative to afferent pupillary defect combined with ocular pain (92%), impaired color vision (94%), and female predominance (77%).¹⁰¹ Most patients begin to recover within 3 weeks from the onset of optic neuritis¹⁰² and >90% of patients have a good recovery in visual acuity of 20/40 or better in 1 year.¹⁰³

As isolated optic neuritis can be idiopathic as well as a manifestation of NMOSD with distinct therapeutic responses and prognoses, differentiation of idiopathic optic neuritis from optic neuritis of NMOSD is important. Relapsing disease course, bilateral simultaneous optic nerve involvements,¹ and poor visual outcome¹⁰⁴ are often the features of NMOSD that may indicate testing for AQP4-Ab.

In patients who are suspected of having an idiopathic optic neuritis, MRI can also yield useful clues in their differential diagnoses and prognoses. As the asymptomatic lesions on brain MRI raise the risk of developing MS (78% in 15 years),¹⁰⁵ lesions on spinal MRI might suggest underlying pathophysiology of NMOSD,¹ and peri-neural enhancement patterns on orbit MRI might imply the presence of antibody against myelin oligodendrocyte glycoprogein (MOG-Ab).^106,107

Interestingly, even within idiopathic optic neuritis, there is a diverse range of prognoses, ranging from isolated optic neuritis, relapsing isolated optic neuritis, or chronic relapsing inflammatory optic neuropathy,¹⁰⁸ thus suggesting a heterogeneous pathogenesis of idiopathic optic neuritis.

Inflammatory diseases associated with antibody to myelin oligodendrocyte glycoprotein

The myelin oligodendrocyte glycoprotein (MOG) is a member of the immunoglobulin superfamily, and is expressed on the surface of oligodendrocytes and myelin.¹⁰⁹ Although the presence of MOG-Ab in a subgroup of patients with inflammatory demyelinating disease of the CNS has been an important issue, clinical implications of this antibody in earlier studies were highly controversial.^110,111 Most of these controversies seem to stem from the methodological issues in the antibody assays, such as the selection of (1) linearized or denatured MOG proteins,¹¹² (2) short-length or full-length MOG, or (3) secondary antibody against human IgG (H + L).¹¹³ At this time, the cell-based assay with the full length of human MOG-transfectant and secondary antibody against human IgG1 seem to be most useful in detecting conformation-sensitive MOG-Ab with clinical implications.^113,114

The inflammatory diseases associated with MOG-Ab can manifest as a phenotype of NMOSD because they frequently have recurrent or bilateral optic neuritis^106,115 and/or LETM.^115,116 Nevertheless, in an adult cohort of inflammatory disease, MOG-Ab-positive patients differed from the NMOSD-AQP4 group in that the former more frequently manifested as isolated optic neuritis (83% versus 8%, respectively), had more optic nerve involvements at onset (82% versus 37%), fewer spinal cord relapses (0% versus 84%), and fewer relapsing disease courses (29% versus 90%). Interestingly, the MOG-Ab-positive patients showed a characteristic MRI feature of peri-neural enhancement on orbital MRI, which was observed in neither MS nor NMOSD with AQP4-Ab (Figure 2).¹⁰⁶ In pediatric cohorts, MOG-Ab was frequently found in patients with ADEM (up to 43%), most of whom had two or more episode of attacks (up to 100%).¹¹⁷

Figure 2.

Peri-neural enhancement pattern in orbit MRI of MOG-Ab-associated optic neuritis.

As inflammatory disease with MOG-Ab had distinctive radiological, clinical, and prognostic features from both MS and NMOSD-AQP4,¹⁰⁶ and also as the MOG-Ab were rarely found among patients with AQP4-Ab,^106,115,116 this MOG-Ab may be a specific biomarker for a disease that has a distinct pathogenic mechanism. Nevertheless, further studies, especially on the optimal assay method for detecting MOG-Ab, are needed for the exact clinical utility of this autoantibody.

Interestingly, a recent multicenter study on a cohort in Europe reported that one-third of patients with MOG-Ab can also have brainstem involvements ranging across diverse symptoms from asymptomatic cases to fatal rhombencephalitis,¹¹⁸ some of which might mimic brainstem involvements of NMOSD-AQP4.

Sarcoidosis

Sarcoidosis is a systemic granulomatous disease that commonly involves the lymph node, skin, lung, eye, and nervous system. The incidence of sarcoidosis is estimated to be 10.9–35.5 cases per 100,000, which was higher among female African Americans.¹¹⁹ Though a limited number (5–15%) of patients with sarcoidosis experience clinical involvement in the nervous system (neurosarcoidosis), both the optic nerve and the spinal cord seem to be relatively frequently involved.¹²⁰ Moreover, the optic nerve (Figure 3) and spinal cord (Figure 4) involvement in neurosarcoidosis can be bilateral and longitudinally extensive, respectively,^121,122 which resembles the phenotypes of NMOSD.¹ As most patients with neurosarcoidosis can have systemic involvements of sarcoidosis, searching for the systemic manifestations of sarcoidosis, such as bilateral hilar adenopathy on chest radiography (Figure 3), erythema nodosum, uveitis, or macular/papular skin lesions, may be first diagnostic clues.^123,124 Nevertheless, in neurosarcoidosis cases without systemic involvements, histopathologic evaluation of the CNS tissue may be needed to confirm the diagnosis.^121,125 In addition, fluorodeoxyglucose positron emission tomography (FDG-PET) can be useful in both identifying the systemic involvement of sarcoidosis and deciding on the biopsy site.^121,126 Currently, two sets of diagnostic criteria for neurosarcoidosis are available.^125,127 Among those, the most recent criteria of the World Association of Sarcoidosis and Other Granulomatous Diseases (WASOG) suggested a category of highly probable neurosarcoidosis in the presence of a clinical picture consistent with granulomatous inflammation of the nervous system plus MRI findings of neurosarcoidosis or CSF examination suggestive of inflammation.¹²⁷

Figure 3.

Right optic neuropathy and thoracic lymphadenopathies in patients with sarcoidosis.

Figure 4.

Neurosarcoidosis manifesting LETM.

LETM in sarcoidosis can be differentiated from LETM in NMOSD in that the former has a greater prevalence of elevated angiotensin converting enzyme, dorsal cord subpial gadolinium enhancement extending over two or more vertebral segments, and persistent contrast-enhancement (>2 months),¹²¹ but these features may not always be present.

CNS involvement in patients with systemic autoimmune disease

Sjogren’s syndrome

Most myelitis cases associated with Sjogren’s syndrome (SS) have longitudinally extensive spinal cord involvement, meet the diagnostic criteria for definite NMO, or are tested positive for AQP4-Ab (Figure 5). Moreover, their clinical, radiological, and prognostic spectrum do not differ from NMO patients without SS.¹²⁸ Given the fact that the AQP4-Ab is not found in SS patients without CNS involvement¹²⁹ and the finding that brain involvement in SS is similar to that in NMOSD,¹³⁰ most of the CNS involvement in SS seem to be the manifestations of coexisting NMOSD rather than the result of the direct CNS involvement in SS.¹²⁸

Figure 5.

Coexistence of the neuromyelitis optic spectrum disorder and SS.

Systemic lupus erythematous

Unlike SS, systemic lupus erythematous (SLE) can involve the CNS (CNS lupus) in a diverse way. Most patients with CNS lupus manifest as headache (54%), seizure (42%), hemiparesis (24%), or memory impairment (24%), and only a small number of patients have optic neuritis (7.3%) or myelitis (4.9%).¹³¹ Though most of these symptoms in CNS lupus are distinct from those in NMOSD,^47,132 some patients with SLE have coexisting NMOSD-AQP4, or vice versa, which could be attributable to a susceptibility to multiple autoimmunity in those patients.^129,133

CNS lymphoma

Primary CNS lymphoma can sometimes be misdiagnosed as NMOSD for a number of reasons. (1) The brain MRI patterns of primary CNS lymphomas are highly variable.¹³⁴ Moreover, brain lesions in NMOSD can frequently be large, confluent, or tumefactive.¹ (2) Both the primary CNS lymphoma (Figure 6) and NMOSD can develop longitudinally extensive spinal cord lesions,¹³⁵ and about 40% of patients with spinal cord lymphoma have intramedullary spinal MRI lesions without swelling of the spinal cord mimicking non-tumorous etiology. (3) Treatment with corticosteroid can, at least initially, lead to an improvement of both clinical symptoms and MRI findings in primary CNS lymphoma.¹³⁶

Figure 6.

Primary CNS lymphoma manifesting as a longitudinally extensive myelitis.

CSF cytology (sensitivity of 2–32%),¹³⁷ immunoglobulin heavy chain (IgH) rearrangement testing (sensitivity of 58% and specificity of 85%),¹³⁸ and other molecular diagnostic testing may help with the diagnosis of CNS lymphoma to some extent. In differentiating CNS lymphoma from NMOSD, position emission tomography (PET) can play an important role as a non-invasive diagnostic tool (Figure 6).¹³⁶ Nevertheless, histopathological confirmation using stereotactic or navigation-guided needle biopsy are recommended for the diagnostic confirmation of CNS lymphoma.¹³⁹

Patients with LETM should be suspected of having primary CNS lymphoma if they continue to worsen, with or without partial initial improvement, despite the combined treatment of methylprednisolone and plasmapheresis, if they show persistent gadolinium enhancement after 3 months of onset, or if they have hypermetabolic lesions on FDG-PET. In patients who are highly suspected to have primary CNS lymphoma, corticosteroid treatment is generally avoided before the biopsy, because it might obscure the histopathological findings.¹³⁹

Neuro-Behçet’s disease

Behçet’s disease (BD) is a multi-systemic vasculitis that can present as painful mucocutaneous lesions combined with diverse systemic involvement. Its prevalence is higher in the Middle East and Pacific Rim than in Western countries (420/100,000 in Turkey versus 5/100,000 in the US).^140,141 Nervous system involvement (neuro-Behçet’s disease, NBD) can be found in a pooled average of 9.4% of BD patients, most of which involve the CNS rather than the peripheral nervous system.¹⁴² CNS involvement of NBD is categorized as either parenchymal (multifocal/diffuse, brainstem, spinal cord, cerebral, or optic nerve) or non-parenchymal (cerebral venous thrombosis, intracranial aneurysm, cervical aneurysm/dissection, or acute meningeal syndrome).¹⁴³ A recent study showed that most (80%) of the spinal cord involvement of NBD was longitudinally extensive lesions, and thereby could resemble LETM of NMOSD¹⁴⁴ (Figure 7).

Figure 7.

NBD manifesting LETM and progressive brain atrophy.

The international study group for BD earlier proposed that the presence of oral ulcers plus two of the following four minor criteria are needed for the diagnosis of BD: genital ulcers, eye lesions, skin lesions, and positive pathergy test.¹⁴⁵ Nevertheless, neurological manifestations in BD can sometimes precede its systemic manifestations, thereby delaying the proper diagnosis of NBD.¹⁴⁶ Recently, two levels of diagnostic criteria for NBD – definite and probable NBD – were proposed in those without systemic manifestations.¹⁴³

The distinctive features of NBD, from those of NMOSD, includes the presence of headache with or without meningoencephalitis (about 70%),¹⁴² a progressive course (38%),¹⁴⁷ and severe brainstem/cerebral atrophy and/or leukoencephalopathy in brain MRI.^148,149 Of note, as spinal cord involvement in NBD is considered a poor prognostic factor (60% of patients became dependent or died after a mean follow-up of 67 months),¹⁵⁰ NBD patients mimicking NMOSD need careful monitoring and intensive treatment.

Spinal dural arteriovenous fistula

Spinal dural arteriovenous fistula (SDAVF) is the most common type of vascular malformation in the spinal cord. It predominantly affects males in their fifth or sixth decades.¹⁵¹ The exact pathophysiology of SDAVF is not entirely clear, but a reduced arteriovenous pressure gradient followed by a decreased tissue perfusion of the spinal cord has been proposed to be causative.¹⁵² Patients with SDAVF mostly experience a subacute onset and progressive myelopathy with acute deteriorations of symptoms after exercise or prolonged rest.¹⁵³ The spinal cord MRI of SDAVF generally reveals longitudinally extensive T2-hyperintense lesions, thereby mimicking LETM of NMOSD. The key radiological difference between SDAVF and LETM in NMOSD when present are the abnormal dilated intradural veins of the spinal cord on T2-weighted MRI (flow void) and/or serpentine enhancing vascular structures on T1-weighted contrast-enhanced MRI, mostly in the dorsal surface of the spinal cord. However, these findings in conventional MRI may not be observed or easily differentiated from the normal vascular structures of the spinal cord, especially in the early stage of disease^154,155 (Figure 8). Though some advocate the use of spinal MR angiography in the diagnosis of SDAVF,¹⁵⁵ catheter angiography remains a diagnostic procedure of choice (Figure 8). SDAVF can be treated by either endovascular embolization or surgical ligation of the fistula.¹⁵⁶

Figure 8.

Two cases of SDAVF.

Infections

Syphilis

Syphilis is a sexually transmitted infectious disease caused by the spirochete bacterium Treponema pallidum (T. pallidum). If not properly treated, this infectious disease can progress through four stages of primary (penetration of the T. pallidum, 10–90 days), secondary (hematogeneous dissemination of the T. pallidum, 4–10 weeks), latent (asymptomatic, up to decades), and tertiary syphilis (localized granuloma or severe diffuse inflammation involving cardiovascular organs or CNS).^157–159

Although optic nerve involvement by syphilis (neurosyphilis-optic neuritis) is relatively uncommon, it causes bilateral severe visual loss and pain that can mimic NMOSD-optic neuritis. It can present in any four stages of syphilis and its mode of onset can be variable, as acute, subacute, or chronic progressive.^160–163

Some neurosyphilis-optic neuritis cases can manifest as optic perineuritis rather than optic neuritis, especially in the early stages, with constricted visual fields and preserved central vision, an atypical pattern for NMOSD-optic neuritis (Figure 9).^162,163 As this neurosyphilis-optic neuritis requires specific treatment, screening for neurosyphilis is important in bilateral optic neuritis cases with poor response to steroid, positive serum treponemal test, history of untreated syphilis, HIV infection and/or constricted pattern of visual field defect.

Figure 9.

Bilateral optic neuropathy in neurosyphilis.

Neurosyphilis can also rarely manifest as a form of LETM that should be treated by intravenous penicillin.¹⁶⁴

Miscellaneous infections

Though rare, infections such as herpes virus (Herpes simplex,¹⁶⁵ Epstein–Barr virus,¹⁶⁶ and cytomegalovirus¹⁶⁷), human T-lymphotrophic virus 1 (HTLV-1),¹⁶⁸ dengue virus,¹⁶⁹ Borrelia burgdorferi (Lyme),¹⁷⁰ tuberculosis,¹⁷¹ Mycoplasma pneumoniae,¹⁷² and Streptococcus pneumoniae¹⁵ can manifest as LETM and/or optic neuritis.

The differential diagnosis of infectious LETM from NMOSD-LETM can sometimes be challenging as some NMOSD cases can show high pleocytosis.¹⁷ Nevertheless, infectious myelitis can differ from NMOSD-LETM, in that the former can have either fever with high C-reactive protein/low CSF glucose level (bacterial), history of pulmonary tuberculosis with low CSF adenosine deaminase level (tuberculosis), chronic progressive course (HTLV-1), presence of the skin lesion, or diffuse arthralgia (miscellaneous). Moreover, AQP4-Ab is not detected in the sera of patients with most of the infectious myelitis. If infectious etiology were suspected in patients with LETM, further evaluations including culture of the specific infectious agents, PCR analysis, and serology for the specific infectious agent are needed. If bacterial LETM cannot be ruled out in the initial diagnostic phase (with AQP4-Ab serostatus unavailable), antibiotics and steroid may be administered according to the management of bacterial meningitis, pending the AQP4-Ab serostatus.

Interestingly, though most of the infectious myelitis cases reported absence of AQP4-Ab,^15,166–173 several cases have shown that NMOSD with AQP4 can develop several days after zoster infection.^174–176 These findings might imply at least some pathogenic overlap between these two distinctive diseases of NMOSD and herpes zoster.

Leber hereditary optic neuropathy

Leber hereditary optic neuropathy (LHON) is an inherited optic neuropathy caused by mutations in the mitochondrial DNA (the three most common mitochondrial mutations in LHON are at nucleotide positions 11778, 14484, and 3460).¹⁷⁷ It predominantly affects males (80%) in their second or third decade of life and is probably one of the most common hereditary optic neuropathies, with a prevalence of more than 3.22 per 100,000 in northeast England.¹⁷⁸ Although it is an inherited disease, only about 40% of LHON patients are aware of their family member having symptoms of LHON, which could be attributable to the low penetrance of LHON (only 27% in males and 8% in females).¹⁷⁹ It mostly manifests as bilateral simultaneous or consecutive painless central scotoma that progress to visual loss over weeks or months (Figure 10). Currently, there is no established treatment for LHON and most patients are left with bilateral visual acuities ⩽20/200.¹⁸⁰ The major difference compared to NMOSD-optic neuritis is the male predominance, more progressive course, more bilateral optic nerve involvement from onset, presence of a family history, absence of gadolinium enhancement in the optic nerve on MRI, absence of the response to immune-modulating/suppressing treatment, and mutations in the mitochondrial DNA. Interestingly, some patients with LHON can have systemic involvement beyond the optic nerve (LHON-plus), including the brain and the spinal cord, just like the CNS lesions seen in MS. A recent report suggested that the spinal cord involvement of LHON-plus could be distinctive from that of NMOSD in that the former involved predominantly the posterior column of the spinal cord.¹⁸¹

Figure 10.

Progressive visual field defect in a patient with LHON.

Conclusion

Diverse neurological diseases including inflammatory, infectious, malignant, vascular, and hereditary etiologies can resemble the phenotypes of NMOSD. Nevertheless, as these NMOSD-mimics are distinct from NMOSD in treatment as well as pathophysiology, early differential diagnosis and appropriate individualized treatment will improve the outcome of such patients.

Footnotes

Acknowledgements

The authors thank Ms. Chihiro Ono for secretarial assistance.

Funding

This work was supported in part by the Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (#26293205), by the Grants-in-Aid for Scientific Research from the Ministry of Health, Welfare and Labor of Japan, and by grant No. 2014R1A1A2055741 from the Korea National Research foundation fund.

Conflict of interest statement

Prof. Kazuo Fujihara serves on scientific advisory boards for Bayer Schering Pharma, Biogen Idec, Mitsubishi Tanabe Pharma Corporation, Novartis Pharma, Chugai Pharmaceutical, Ono Pharmaceutical, Nihon Pharmaceutical, Merck Serono, Alexion Pharmaceuticals, Medimmune and Medical Review; has received funding for travel and speaker honoraria from Bayer Schering Pharma, Biogen Idec, Eisai Inc., Mitsubishi Tanabe Pharma Corporation, Novartis Pharma, Astellas Pharma Inc., Takeda Pharmaceutical Company Limited, Asahi Kasei Medical Co., Daiichi Sankyo, and Nihon Pharmaceutical; serves as an editorial board member of Clinical and Experimental Neuroimmunology (2009 to present) and an advisory board member of the Sri Lanka Journal of Neurology; has received research support from Bayer Schering Pharma, Biogen Idec Japan, Asahi Kasei Medical, The Chemo-Sero-Therapeutic Research Institute, Teva Pharmaceutical, Mitsubishi Tanabe Pharma, Teijin Pharma, Chugai Pharmaceutical, Ono Pharmaceutical, Nihon Pharmaceutical, and Genzyme Japan.

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Differential diagnosis of neuromyelitis optica spectrum disorders

Abstract

Keywords

Introduction

Diagnosis of NMOSD

The AQP4-Ab assay: implications and caveats

Differential diagnosis of NMOSD

Multiple sclerosis

Acute disseminated encephalomyelitis

Idiopathic acute transverse myelitis

Idiopathic optic neuritis

Inflammatory diseases associated with antibody to myelin oligodendrocyte glycoprotein

Sarcoidosis

CNS involvement in patients with systemic autoimmune disease

Sjogren’s syndrome

Systemic lupus erythematous

CNS lymphoma

Neuro-Behçet’s disease

Spinal dural arteriovenous fistula

Infections

Syphilis

Miscellaneous infections

Leber hereditary optic neuropathy

Conclusion

Footnotes

Acknowledgements

Funding

Conflict of interest statement

References