Syringomyelia-like syndrome in neuromyelitis optica spectrum disorder complicated with Sjogren’s syndrome: a case report
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Besides CSF-flow obstruction, syringomyelia is associated with inflammatory spinal cord lesions. However, syringomyelia-like syndrome concomitant with neuromyelitis optica spectrum disorder (NMOSD) and primary Sjogren’s syndrome (pSS) is extremely rare. Here, we would like to report a case of a patient with syringomyelia-like syndrome in NMOSD complicated with Sjogren’s Syndrome.
A 64-old male Han Chinese, presented with three episodes of acute demyelinating processes in the central nervous system within 5 years. Firstly, he presented with ascending left lower extremity weakness and numbness, and initially progressive loss of vision in the right eye before 5 years, and subsequently in the right eye 2 months later. High dose corticosteroid therapy was prescribed for this attack. Second, he suffered from refractory gastrointestinal symptoms.
such as nausea, vomiting, abdominal pain and early satiety. After the second episode, he received long-term azathioprine and prednisone treatment in low dosages. Six months before admission, he developed the lower back pain and numbness in lower limbs, and urinary incontinence. This time, he complained of acute onset of right lower limb paralysis, paresthesia and urinary incontinence. MRI of the spine revealed a syringomyelia extending from the C7 to T4 levels with serum positive anti-aquaporin-4 antibodies (AQP4-Ab) (indirect immunofluorescence on AQP4 transfected cells). he was serologically positive for both anti-Sjögren’s syndrome-related antigen A and B antibodies and there was reduced salivary flow on scintigraphy. Lip salivary gland (LSG) biopsies were graded (grade four lymphocytic infiltration) according to the Chisholm and Mason classification system and by morphometric analysis. And finally, diagnosed as syringomyelia-like syndrome in NMOSD complicated with Sjogren’s syndrome.
Although extremely rare, This index patient highlights that syringomyelia could be associated with underlying NMOSD and pSS, and autoimmune disorders should be considered in the initial differential diagnosis, This is very helpful for the therapeutic implications and evaluating curative effect.
KeywordsNeuromyelitis optica spectrum disorder Aquaporin-4 antibodies Oligoclonal bands Syringomyelia-like syndrome Sjogren’s syndrome
Neuromyelitis optica spectrum disorder
Syringomyelia is a chronic, progressive and degenerative disorder, characterized by a cystic or cavitary formation within the spinal cord. The exact pathogenesis and development of syringomyelia is uncertain. Syringomyelia coexisting with multiple sclerosis (MS) has been described in various case reports/series. However, literatures describing syringomyelia coexisting with neuromyelitis optica spectrum disorder (NMOSD) and primary Sjogren’s syndrome (pSS) are extremely rare, and only a few syringomyelia in NMOSD have been reported [1, 2, 3, 4, 5]. We report a case of syringomyelia-like syndrome coexisting with NMOSD and pSS.
Discussion and conclusion
Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune inflammatory disease of the central nervous system (CNS) associated with antibodies against aquaporin 4 (AQP4), the target antigen of NMO-IgG was confirmed to be AQP4, the water channel protein which mainly expressed on astrocytic foot processes at the optic nerves, spinal cord, and certain areas of the brain. The cervical and thoracic cords are the most frequent sites involved in NMOSD, resulting in subsequent motor and sensory deficits presentations. Similarly, the common signs and symptoms of syringomyelia include muscle weaknesses, absence of pain, temperature sensations, and these symptoms often fluctuate in severity and duration, vary widely depending on the extent and the location of the syrinx inside the spinal to develop slowly but also occur abruptly [6, 7]. Many cases of syringomyelia have been reported as an incidental finding in multiple sclerosis (MS) or NMO [2, 8, 9, 10]. Syringomyelia.
during the course of the disease in patients presenting with clinically definite MS has been described in 4.5% of MS patients [8, 10]. However, there is only limited information regarding syringomyelia and NMOSD.
We evaluated many possible causes of syringomyelia in our patient. Finally diagnosis of the syringomyelia coexisting with NMOSD and pSS was confirmed. Other causes of myelopathy was excluded neurosarcoidosis sarcoidosis [11, 12], Behcet’s disease, vitamin B12 hypovitaminosis, and so on. The evaluation revealed a syringomyelia throughout the thoracic cord, from the C7 to T4 levels with anti-aquaporin-4 antibodies(NMO-IgG is a disease-specific autoantibody against AQP4 for NMOSD)positive and oligoclonal bands negative [13, 14]. Anti-Sjogren’s syndrome A and B antigen antibodies were positive, and there was reduced salivary flow on scintigraphy. Salivary gland biopsy showed lymphocytic infiltration. Sjogren’s syndrome met the diagnostic criteria of the 1968 Chisholm & Mason . the clinical, serological, pathological biopsy and image features were fully consistent with the diagnosis of syringomyelia coexisting with NMOSD and pSS.
Growing evidence suggests autoimmune diseases more likely represent coexistent NMOSD rather than neurological complications of them. The wide spectrum of neurological manifestations in pSS have been reported, the prevalence of neurological symptoms of pSS range from 8.5 to 70%. However, Central nervous system (CNS) involvement is not common in PSS, approximately 2 to 25%, vary in presentation from focal, multifocal to additive or progressive, accompanying with a clinical course of fixed or cumulative deficits [16, 17]. The occurrence of myelopathy in pSS appears to be far from exceptional. Spinal cord involvement counld develop severe acute syndrome (acute transverse myelitis) or chronic progressive myelopathy [19, 20, 21, 22]. Acute transverse myelitis is the most common form of spinal cord involvement in the course of pSS. The spectrum of clinical symptoms are diverse, relating to the region of the lesion. Our patient showed both prior acute attack and chronic progressive condition. pSS presenting as chronic progressive myelopathy, although rare, has previously been reported [19, 20, 21, 22].
The exact mechanism of syringomyelia formation in the setting of NMOSD and Sjögren syndrome remained unclear [18, 23]. Increasing evidence about AQP4-IgG antibody binding to astrocytic AQP4 is involved in the pathogenesis of NMOSD, which causes cascade activation through complement dependent cytotoxicity (CDC), the infiltration of inflammatory cells, blood brain barrier disruption and oligodendrocyte injury and demyelination. Therefore, inflammatory lesions in NMOSD tend to be localized in site of high AQP4 expression, and in central gray matter. The pathogenesis of the gray matter damage is associated with primary selective area of high AQP4 expression, and speculate that anti-aquaporin 4 antibody play a crucial role in development of ‘syringomyelia-like’ syndrome, which causes blood brain barrier disruption, inflammation, necrosis of astrocytes and oligodendroglias, demyelination, and interferes with the circulation of CSF [2, 8, 10]. Other possible reasons include: interaction between the autoantibodies and the multiple targets tissues, shared common genetic, antigens and/or environmental factors which trigger an immune response cross-reacting, immunologic regulation disorder between NMOSD and pSS.
Therefore, Occasional previous reports have indicated that a fluid-filled syrinx-like cavity in the cord may be seen during the acute phase of myelitis in NMOSD. Futhermore, the fluid disappears on follow-up MRI and may not reappear during a subsequent attack of myelitis. This type of fluid accumulation is quite different from the usual type of chronic syringomyelia which is probably related in most cases to obstruction or impairment of CSF flow and not associated with myelitis. Syringomyelia is a consequence of the inflammatory demyelinating pathology or a part of clinical features of the NMOSD with pSS or a coincidental finding in a patient presenting with acute myelitis. Given the limited literature available, further research is necessary to elucidate the relationship between syringomyelia and NMOSD. Especially, long-term follow-up is crucial to clarify the spinal cord fluid in this patient which is transient or chronic. Since NMOSD and pSS coexist together, the diagnosis either condition should warrant further evaluation for the other condition due to potential treatment consideration .
This case report illustrates that ‘syringomyelia-like’ syndrome could be associated with underlying NMOSD and pSS. This finding may further emphasize the necessity and the importance of investigating for autoimmune disorders in ‘syringomyelia-like’ syndrome and subsequent therapeutic implications.
The authors thank BMC Neurology and the reviewers for revising and proofreading the manuscript.
This work was supported by the Shang dong Provincial Nature Fund Joint Special Fund Project(ZR2018LH006); National Natural Science Foundation of China (No. 81870943); Postdoctoral Research Fund of Xuzhou Medical University (NO:2015107026).
Availability of data and materials
All data are presented in the manuscript. There are no additional data.
XL contributed to the concept, drafting and reporting of the case. ZL contributed the reporting and revising the report. YW contributed to the analysis and interpreting the results and revising the report. All authors read and approved the final manuscript. All authors read and approved the contents of the case report.
Ethics approval and consent to participate
This research was approved by the ethics committee of the Affiliated Hospital of Wei fang Medical University and the patient gave written informed consent prior to obtain the data. This study was performed in accordance with the Declaration of Helsinki and all authors agreed the publish statements of BMC Neurology. All authors have no competing interests or conflicts of interest declare.
Consent for publication
Ethic approval was waived as a case report, and the consent to participate was obtained from the patient in a written informed consent form including the consent for the publication of all the personal, medical details and images.
The authors declare that they have no competing interests.
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