Recurrent post-partum rhombencephalitis associated with anti-centromere antibody: A case report

doi:10.21203/rs.2.89/v1

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Case Report

Recurrent post-partum rhombencephalitis associated with anti-centromere antibody: A case report

https://doi.org/10.21203/rs.2.89/v1

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published 14 Oct, 2019

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Background

Rhombencephalitis (RE) is a serious condition of the brain with multiple etiologies. We report a unique case of recurrent, postpartum RE that is associated with positive anti-centromere antibody (ACA). A discussion of the case, current literature on autoimmune RE and related autoantibodies are reviewed.

Case Presentation

A healthy 33-year-old Caucasian patient (gravida 2, para 2) had two episodes of progressive focal neurological deficits during postpartum periods. Signs and symptoms included right-sided dysmetria, adiadochokinesia, weakness, ataxia, and photophobia. MRI revealed rhombencephalitis involving the mesencephalon. Extensive and comprehensive investigations using blood and cerebrospinal fluid (CSF) were consistently positive only for ACA. The first episode was successfully treated with empiric antimicrobial agents and steroid. Given the negative infectious work up with the prior episode and the nearly identical clinical presentations, the second episode was treated with corticosteroid only. This led to complete resolution of her symptoms and reversal of the brain magnetic resonance imaging (MRI) lesions.

Conclusion

To the authors’ knowledge, this is the first report of a primary autoimmune RE during postpartum period that is associated with ACA. Immunologic causes should be considered early with any encephalitis. Given the risk of recurrence, relapse, and neurologic deterioration, regular monitoring is recommended, especially for female patients of child-bearing age. Consistent with the current literature on autoimmune RE, steroid seems to be an effective treatment for ACA-associated RE.

Keywords: Autoimmune disease, rhombencephalitis, anti-centromere antibody, connective tissue disease, case report

Internal Medicine Specialties

Autoimmune disease

rhombencephalitis

anti-centromere antibody

connective tissue disease

case report

Rhombencephalitis (RE) is a rare inflammatory disease affecting the hindbrain. Without prompt diagnosis and treatment, severe and life-threatening complications may ensue (1). Multiple etiologies, including infection, paraneoplastic syndrome, and autoimmune disorders, have been identified to date (1,2). Although less common, autoimmune RE may develop without an underlying immunologic disease or malignancy (3–5). A primary autoimmune RE by definition is associated with specific neuronal antibodies, and a handful have been identified to date, including anti-NMDA, anti-GAD65, and anti-Hu (6). To the best of our knowledge, there are no previous reports showing a direct link between RE and anti-centromere antibody (ACA). With an informed consent of the patient, we report a unique case of primary autoimmune RE. She was gravida two and para two; both of her postpartum periods were plagued by RE, the first of which fully resolved with treatment, only to recur after the birth of a second child. The patient was consistently seropositive for ACA. Similar to the treatment of general autoimmune encephalitis (6,7), methylprednisone proved effective for ACA-associated RE.

A healthy 33-year-old, right-handed Caucasian patient experienced two episodes of post-partum RE in 2015 and 2017 (Fig. 1). The first episode occurred five months after a normal vaginal delivery of her first child. She presented to the emergency department with progressively worsening right-sided dysmetria, adiadochokinesia, weakness, ataxia, and photophobia. Past medical history showed that the patient was well. The patient had other than an infectious mononucleosis at age 16. She started progestin oral contraceptives a few months after the deliveries and had no known allergies. She denied any substance use, including alcohol, tobacco, and recreational drugs. Review of systems and physical examinations were otherwise unremarkable. The patient’s mother had systematic lupus erythematous (SLE).

Gadolinium-enhanced MRI revealed a large area of FLAIR (Fluid attenuated inversion recovery) and T2 hyperintensity that crossed the midbrain but did not involve the colliculi nor the pons, suggesting a form of RE (Fig. 2). Extensive investigations with blood and cerebrospinal fluid failed to yield any underlying etiology, such as infectious, metabolic, vascular, or demyelinating disease. Potentially abnormal findings included the following: CBC with neutrophilia (7,800 cells/µL) and leukocytosis (5,000 cells/µL); CSF analysis with albumin 53.1 mg/dl (37-51), α1 globulin 5.4% (6.1-10.5), and β globulin 3.9% (4-7.2); and viral serology with positive Epstein-Barr virus IgG and nuclear antigen, but negative IgM. Although she had no underlying autoimmune condition, the ANA screen came back positive for ACA.

Viral and atypical infections tested were Human immunodeficiency virus, Enterovirus, Herpes simplex, Cytomegalovirus, Varicella Zoster, Powassan virus, Eastern equine encephalitis, Jamestown Canyon virus, arbovirus, West Nile virus, Toxoplasma, Mycobacterium tuberculosis, Treponema pallidum, Listeria monocytogenes, and Borrelia burgdorferi. Autoimmune screening included oligoclonal band, anti-NMO antibodies, cryoglobulins, complement levels, thyroid antibodies, and other autoimmune antibody panels associated with encephalitis and paraneoplastic syndrome. Conditions, including collagen disease, vasculitis, stroke, Behçet, and Hashimoto encephalopathy, could not be diagnosed with established criteria. Based on these findings and clinical symptoms, RE was diagnosed. Without a clear etiology, the patient was treated empirically with parenteral acyclovir 600 mg, ampicillin 2 g, and methylprednisolone 1 g. Complete resolution of symptoms and reversal of radiologic abnormalities were achieved.

Four months after the delivery of a second child, the patient presented to the ER with an acute onset of right-sided dysmetria, weakness, ataxia, photophobia, and blurred vision on the left eye. She was admitted to the hospital and seen by neurology. Physical exam revealed a slight relative afferent pupillary defect on the left eye and mild blurring of the optic disk bilaterally with normal visual field and extra-ocular movements. Comprehensive investigations were conducted with additional tests in cytology and microbiology. Whipples disease and potential malignancies were ruled out.

T2-FLAIR MRI showed hyperintensity involving the same region of midbrain, but less extensive than the one observed in the first episode, suggesting that the patient had a recurrent RE. The patient was again positive for ACA. The rest of the exams and tests were essentially normal. Given the negative infectious work up in the prior episode and the nearly identical clinical presentations, we decided to treat the patient with corticosteroid, notably IV methylprednisolone 500 mg. This fully reversed her clinical symptoms and MRI lesions with no serious adverse events. At 10 months follow-up, routine investigations and examinations were normal with no residual neurological deficits. However, ACA remained positive.

Rhombencephalitis (RE) affects individuals of all ages, sex, ethnicity, and immune status (4,8,9). Listeria monocytogenes and other infectious inflammatory causes are often cited as the most common etiology of RE (10,11). However, some studies have reported a higher proportion of immunological etiologies, causing autoimmune RE (4,8). This happens when autoantibodies target crucial biochemical components within the brainstem and/or cerebellum. Depending on the antibody involved in the inflammatory process of autoimmune RE, the initial symptoms may differ. Common initial findings for Anti-NMDAR RE include psychosis, memory impairment, dysmetria, and/or seizures (12). Anti-Hu RE patients usually present with multifocal involvement of the brain that includes cerebellum and medulla, leading to cranial nerve and motor abnormalities (13). This highlights that identifying the antibody that is associated with the suspected autoimmune RE is crucial. It may allow the treating physicians to obtain information for treatment, prognosis, and diagnosis of the underlying immunologic or neoplastic disease (6).

Autoimmune RE may occur secondary to autoimmune disease or paraneoplastic syndromes (2,7–9,14,15), but may occur without an underlying etiology – primary autoimmune RE (4,6). In this present case, the patient‘s disease can be classified as a probable primary autoimmune RE, given the lack of a defined autoimmune disease or paraneoplastic syndrome. There seems to be a link between the pregnancy and the onset of the disease following the delivery. The first episode of the autoimmune RE observed for this patient occurred during the postpartum period following the first pregnancy; and the same inflammatory process came back following the second pregnancy/delivery. Some cases of postpartum onset have been reported for anti-NMDAR encephalitis (16). The underlying mechanism is not clear. This case extends the list of primary RE that occurs during the postpartum period.

It is intriguing to speculate about the timing of the recurrent RE, as well as the positive ACA. To the best of our knowledge, this is the first case of primary autoimmune RE associated with ACA. Previous studies have linked ANA to primary autoimmune RE with unknown etiology (4). ACA is found in 13.4% of individuals with Sjögrens (17) and 50-96% with limited systemic scleroderma, also known as CREST syndrome (18). Acute disseminated encephalopathy was reported in a patient with ACA-positive Sjögren that affected bilateral cerebral hemispheres, mainly within the white matter (19). Even though it is rare, scleroderma may present with neurological manifestations involving the brainstem; and in that case it might mimic RE (20). In our case, the patient did not meet the diagnostic criteria for Sjögrens nor scleroderma. This is therefore a new case of primary autoimmune RE associated with ACA.

ACA-associated RE seems to represent a unique subset of primary autoimmune RE that has autoantibodies with unknown effects on neurons. Other similar examples include anti-SSA and anti-MOG associated with Sjögrens and demyelinating diseases respectively (7,21). The precise role and prognostic value of ACA in the development and progression of autoimmune RE are unclear. There is no data to guide long-term treatment. Due to the potential for recurrence, relapse, and worsening degree of neurological symptoms in primary autoimmune RE, however, close monitoring of the patient is warranted, especially among women of child bearing age. Having a positive family history of SLE in conjunction with ACA, the patient may also have a higher probability of developing a connective tissue disease and thus may benefit from a long-term follow-up.

In conclusion, this case study reports an unusual case of recurrent postpartum, primary autoimmune RE in association with a positive ACA. We speculate there may be a causal association. In general, the diagnosis necessitates antibody testing of CSF, brain imaging, and exclusion of other causes of encephalitis, including infection, autoimmune disorders, drugs, and malignancy. Immunologic causes should be considered early with any encephalitis, given the risk of rapid deterioration and highly effective steroid treatment. A positive ACA status in the context of RE may guide acute treatment and long-term management. This paper supports the current consensus available for autoimmune RE – to use steroid as the first-line therapy for ACA-associated RE. Further investigations on the functions of ACA in neurons are needed to better understand the pathophysiology.

ACA: Anti-centromere antibody; ANA: Anti-nuclear antibody; CSF: Cerebrospinal fluid; FLAIR: Fluid attenuated inversion recovery; MOG: Myelin oligodendrocyte glycoprotein; MRI: Magnetic resonance imaging; NMDAR: N-methyl-D-aspartate receptor; SLE: Systemic lupus erythematous; SSA: Sjögren’s syndrome related antigen A; RE: Rhombencephalitis

Acknowledgements

The authors would like to thank the patient, medical staffs, and physicians, Dr. Théophile Thériault, Dr. Émilie Bazinet, and Dr. Remi Leblanc, who were involved in the management of this patient and made it possible to report this case.

Funding

There was no funding for this study.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Author’s contributions

AM, BH, and AJ carried out the clinical examination of the patient and they have contributed to the clinical description. AJ gathered all clinical data, carried out literature review and wrote the manuscript. JM carried out literature review and contributed to the redaction of the manuscript. All authors critically reviewed the manuscript for the relevance of intellectual content and for appropriate language. All authors approved the final manuscript.

Ethics approval and consent to participate

Ethics proposal was reviewed and approved on August, 2018, by Research Ethics Board of Vitalité Health Network, New Brunswick, Canada.

Consent for publication

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the editor of this journal.

Competing interests

Authors have no conflict of interest.

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