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01.12.2017 | Case report | Ausgabe 1/2017 Open Access

Journal of Medical Case Reports 1/2017

Opsoclonus myoclonus syndrome in a patient with Japanese encephalitis: a case report

Zeitschrift:
Journal of Medical Case Reports > Ausgabe 1/2017
Autoren:
Subatharshini Sountharalingam, H. M. M. T. B. Herath, Dharshana Wijegunasinghe, Sunethra Senanayke
Abbreviations
ACTH
Adrenocorticotropic hormone
ALT
Alanine aminotransferase
AST
Aspartate aminotransferase
bpm
Beats per minute
CSF
Cerebrospinal fluid
EEG
Electroencephalogram
FLAIR
Fluid-attenuated inversion recovery
JE
Japanese encephalitis
K
Potassium
MRI
Magnetic resonance imaging
Na
Sodium
NMDA
N-methyl-D-aspartate
OMS
Opsoclonus myoclonus syndrome
SpO2
Blood oxygen saturation
WHO
World Health Organization

Background

Japanese encephalitis (JE) is a mosquito-borne viral encephalitis caused by a Flavivirus closely related to West Nile and St. Louis encephalitis viruses [1]. Humans are an incidental dead-end host while pigs and birds are the amplifying hosts. The culicine mosquito species Culex tritaeniorhynchus and Culex gelidus are the principal vectors. However, some other culicine mosquito species such as Culex vishnui, Culex pseudovishnui, and Culex fuscocephala are also responsible for the transfer of the virus to humans from amplifying hosts [1, 2]. A majority of infections are asymptomatic and only less than 1% manifest as encephalitis [1]. Nearly 35,000 to 50,000 cases of JE are reported to the World Health Organization (WHO) each year, resulting in an estimated 10,000 to 15,000 deaths annually. The case fatality rate varies between 5 and 30%, while 30 to 50% of survivors have significant neurological sequelae [1].
The clinical course is divided into prodromal phase, acute encephalitic stage, and late phase. The prodromal phase starts before the onset of encephalitis, with fever and constitutional symptoms. Altered sensorium, nuchal rigidity, and abnormal movements characterize the encephalitic stage. Recovery or persistence of central nervous system signs occurs in the late phase [1]. Cases of opsoclonus myoclonus syndrome (OMS) caused by JE have not been reported previously. Here we discuss a patient with JE who presented with OMS.

Case presentation

A 31-year-old previously healthy Sri Lankan woman from southern parts of Sri Lanka presented with fever for 3 days and altered level of consciousness for 1 day. The fever was associated with headache and myalgia and she did not have nausea, vomiting, or skin rashes. On admission to our hospital she was afebrile and nuchal rigidity was present. She was conscious but aphasic. Her Glasgow Coma Scale was 11/15 (E 4, V 1, M 6). There were involuntary conjugate fast eye movements in all the directions of gaze without a saccadic interval, suggestive of opsoclonus. There were no ophthalmoplegia or other cranial nerve palsies. Her pupils were equally reacting to light. Fundoscopy revealed papilledema. There were involuntary twitching movements on the right side of her face, mandible, and tongue, which increased with movement and disappeared during sleep. Both upper and lower limb tone were normal and she was able to move her limbs against gravity, but not against resistance (power 3/5). The deep tendon reflexes were present. Bilateral plantar responses were flexor. Her other vital signs were stable with a heart rate of 68 beats per minute (bpm), blood pressure of 130/80 mmHg, and blood oxygen saturation (spO2) on air was 96%. All other system examinations were unremarkable.
Her full blood count revealed a neutrophil leukocytosis: white blood cells, 14 × 103/μL; neutrophills (N), 78%; lymphocytes (L), 11%; eosinophills (E), 02%; basophills (B), 5%; platelets, 280 × 103/μL; and hemoglobin, 13 g/dl. Her erythrocyte sedimentation rate was 66 mm in the first hour but her C-reactive protein was less than 6 mg/dl. Her serum electrolytes and renal and liver profiles were normal: sodium (Na), 133 mmol/l; potassium (K), 4.5 mmol/l; serum calcium, 2.3 mmol/l; magnesium, 0.99 mmol/l; aspartate aminotransferase (AST), 40 U/l; and alanine aminotransferase (ALT), 47 U/l. Her thyroid stimulating hormone was 0.34 IU/L. Blood and urine culture, blood film for malaria parasite, rheumatoid factor, antinuclear antibody, and human immunodeficiency virus serology were negative. Thyroid microsomal antibody was less than 10 IU/ml and N-methyl-D-aspartate (NMDA) receptor antibody was also negative. A non-contrast computed tomography of her brain showed cerebral edema. Cerebrospinal fluid (CSF) opening pressure was 180 mmH2O and full report showed high level of proteins of 130 mg/dl with 60 lymphocytes/mm3. Polymorphs and red blood cells were absent in CSF. CSF glucose was 3.4 mmol/l (corresponding random blood sugar was 5.5 mmol/l). Herpes simplex virus polymerase chain reaction in CSF was negative. IgM for JE became positive in both serum and CSF. Magnetic resonance imaging (MRI) of her brain showed symmetrical bilateral high signal intensities in basal ganglia, head of the caudate, and midbrain in T2 and fluid-attenuated inversion recovery (FLAIR) without diffusion restriction (Fig. 1). Serial electroencephalograms (EEGs) were done which showed various epileptiform discharges. Initial EEG showed bilateral periodic lateralized epileptiform discharges (Fig. 2) and the second EEG after 2 days showed left-sided lateralization with background slowing.
She was given supportive care and once JE was confirmed we administered methylprednisolone pulses intravenously (1000 mg per day) for 5 days. With this, she improved gradually with reduction in opsoclonus and myoclonic movements. Her limb muscle power and speech also improved slowly. After approximately 2 weeks of the disease duration, epileptic discharges and background slowing in an EEG showed improvement. During the course of her illness she became rigid and a quarter of a tablet of levodopa-carbidopa (250/25 mg) was started at a frequency of three times a day to alleviate the extrapyramidal symptoms.

Discussion

Viral encephalitis classically causes fever, headache, altered sensorium, neuropsychiatric manifestations, catatonia, and abnormal movements such as orolingual tremors, myokymia, and lip smacking, and mandibulo-faciolingual tremors are also reported [3, 4]. Even though OMS is not commonly caused by infections, there are case reports of viral encephalitis which had caused OMS such as varicella zoster, West Nile encephalitis [5], and mumps [6]. OMS after influenza vaccination was also reported [7] and in India OMS due to malaria had been reported [8].
OMS also known as myoclonic encephalopathy (Kinsbourne syndrome) and “dancing eyes-dancing feet syndrome”, is a rare neurological disorder that occurs at a prevalence of 1 in 10,000,000. It usually occurs in children with neuroblastoma as a paraneoplastic manifestation and in adults due to underlying lung cancer and gynecological malignancies. Toxins and autoimmune diseases like Hashimoto encephalopathy are known to cause OMS as well [9]. Opsoclonus is defined as chaotic, conjugate, multivector, back-to-back, saccadic eye movements without intersaccadic latency. It is also called saccadomania [9]. It is thought to occur due to damage of the omnipause cells in the pontine raphe nucleus [9]. Our patient had opsoclonus and involuntary twitching movements of the right side of her face suggestive of myoclonus. Ataxia and cerebellar involvement could not be assessed in our patient.
Diagnosis of JE depends on imaging and CSF analysis. Characteristic MRI appearance is T2 and FLAIR hyperintensities in thalamus, basal ganglia, caudate, and midbrain bilaterally. Although CSF pressure is elevated in approximately 50% of cases, it was normal in our patient. A CSF full report showed elevated protein with CSF lymphocytosis typical of JE. JE-specific IgM antibody was positive in CSF as well as in serum in the second week of illness. Ultrasound imaging of her abdomen and a chest X-ray that were done to exclude underlying malignancies were normal. Hashimoto encephalopathy and autoimmune encephalitis also can cause a similar clinical picture but thyroid peroxidase antibody and NMDA receptor antibody were negative in our patient.
Various therapies have been tried successfully in patients with OMS and they include corticosteroids, intravenously administered immunoglobulin, immunosuppressants, plasma exchange, rituximab, adrenocorticotropic hormone (ACTH), and clonazepam. In our case, a significant improvement was observed with intravenously administered methylprednisolone pulses over a short period of time. Parkinsonism features improved dramatically after a small dose of levodopa-carbidopa.

Conclusions

We intended to highlight that OMS can also be a feature of JE and that this virus can be added to the list of viruses that can cause OMS. Currently there is no well-accepted treatment in OMS and intravenously administered methylprednisolone pulses and immunosuppressants can be used successfully in these patients for early recovery.

Acknowledgements

This case report was supported by doctors working in Ward 16, National Hospital of Sri Lanka, in acquisition, analysis, and interpretation of data. We are thankful to the patients’ relatives for the support given in providing data.

Funding

No source of funding.

Availability of data and materials

The datasets supporting the conclusions of this article are included within the article.

Ethics approval and consent to participate

Not applicable.

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-in-Chief of this journal.

Competing interests

The authors declare that they have no competing interests.

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