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Case Report Diplopia: A Rare Manifestation of Neuroborreliosis Ayushi Dixit , 1 Yesika Garcia, 1 Lauren Tesoriero, 2 Charles Berman, 1 and Vincent Rizzo 1 1 NYC Health + Hospitals/Queens, Icahn School of Medicine at Mount Sinai, USA 2 New York Institute of Technology College of Osteopathic Medicine, USA Correspondence should be addressed to Ayushi Dixit; [email protected] Received 2 February 2018; Revised 22 May 2018; Accepted 25 June 2018; Published 9 July 2018 Academic Editor: Chin-Chang Huang Copyright © 2018 Ayushi Dixit et al. is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Early disseminated Lyme disease typically presents with cardiac, rheumatologic, or neurologic symptoms. ough uncommon, Borrelia burgdorferi can invade the central nervous system and cause neuroborreliosis. In these patients, facial palsy, headache, and stiffness of the neck are the most common presenting symptoms. Our case describes a patient with oculomotor nerve palsy manifesting as double vision as the initial presentation of neuroborreliosis. 1. Introduction Lyme disease is caused by the spirochete Borrelia burgdorferi and is the most common vector-borne disease in the United States. It most commonly presents with erythema migrans or flu-like symptoms. Neuroborreliosis is a term used to describe Lyme disease of the central nervous system. e most common complications of neuroborreliosis include meningitis, facial nerve palsy, and peripheral neuropathy. Diagnosis of the disease is usually clear when the patient recalls a tick bite and/or rash before the onset of symptoms. We present a case of neuroborreliosis manifesting with diplopia. 2. Case Presentation A 69-year-old male with past medical history of type 2 dia- betes and hypertension presented to the emergency depart- ment in New York City in August complaining of headache and diplopia. His headache abruptly began one week ago, was localized to the right occipital region, and gradually moved to his right orbit. Five days later he developed diplopia. One month prior to symptom onset, he hiked in a rural area of New York State, but he denied any tick bites or rash development. On presentation, our patient was hemo- dynamically stable, did not have any signs of acute infection, and denied any fevers or chills. He stated he had double vision when opening both eyes; however if he covered his right eye his vision normalized. Physical exam was significant for leſt sided cranial nerve 3 palsy. e rest of his physical and neurological examinations were normal. MRI and MRA were both negative. Syphilis serology was negative. Lumbar showed glucose of 101, protein of 77, and 74 white blood cells (84% lymphocytes and atypical lymphocytes). CSF was negative for VDRL, cryptococcal antigen, varicella zoster, HSV 1 and 2, and West Nile virus. He had positive Lyme titers by ELISA at 6.04 (negative < 0.90) and western blot showed five IgG and two IgM bands. He was started on acyclovir and ceſtriaxone and experienced resolution of headache but continued to complain of diplopia. Lyme antibody in CSF was checked by ELISA and was reactive at 0.532 (reactive cutoff 0.144). Although the CSF-to-serum ratio of IgG by Eliza was only 0.0880, patient was treated for oculomotor nerve palsy secondary to Lyme meningitis. Acyclovir was discontinued. He was treated with ceſtriaxone for four weeks as per e Sanford Guide to Antimicrobial erapy guidelines. His diplopia resolved and he was asymptomatic two months aſter initiation of therapy. 3. Conclusion is case is an example of a rare presentation of neurobor- reliosis. Although Lyme is known to affect the neurologi- cal system it usually does not manifest in the extraocular muscles. Approximately three-fourths of patients with Lyme- associated cranial neuropathies present with a facial nerve Hindawi Case Reports in Neurological Medicine Volume 2018, Article ID 9720843, 2 pages https://doi.org/10.1155/2018/9720843

CaseReport Diplopia: A Rare Manifestation of Neuroborreliosis · CaseReportsinNeurologicalMedicine palsy[] .Lymediseaserelatedocularcomplicationsare uncommon,butvariousmanifestationshavebeendescribed

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  • Case ReportDiplopia: A Rare Manifestation of Neuroborreliosis

    Ayushi Dixit ,1 Yesika Garcia,1 Lauren Tesoriero,2 Charles Berman,1 and Vincent Rizzo1

    1NYC Health + Hospitals/Queens, Icahn School of Medicine at Mount Sinai, USA2New York Institute of Technology College of Osteopathic Medicine, USA

    Correspondence should be addressed to Ayushi Dixit; [email protected]

    Received 2 February 2018; Revised 22 May 2018; Accepted 25 June 2018; Published 9 July 2018

    Academic Editor: Chin-Chang Huang

    Copyright © 2018 Ayushi Dixit et al. This is an open access article distributed under the Creative Commons Attribution License,which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

    Early disseminated Lyme disease typically presents with cardiac, rheumatologic, or neurologic symptoms. Though uncommon,Borrelia burgdorferi can invade the central nervous system and cause neuroborreliosis. In these patients, facial palsy, headache,and stiffness of the neck are the most common presenting symptoms. Our case describes a patient with oculomotor nerve palsymanifesting as double vision as the initial presentation of neuroborreliosis.

    1. Introduction

    Lyme disease is caused by the spirochete Borrelia burgdorferiand is the most common vector-borne disease in the UnitedStates. It most commonly presents with erythema migransor flu-like symptoms. Neuroborreliosis is a term used todescribe Lyme disease of the central nervous system. Themost common complications of neuroborreliosis includemeningitis, facial nerve palsy, and peripheral neuropathy.Diagnosis of the disease is usually clear when the patientrecalls a tick bite and/or rash before the onset of symptoms.We present a case of neuroborreliosis manifesting withdiplopia.

    2. Case Presentation

    A 69-year-old male with past medical history of type 2 dia-betes and hypertension presented to the emergency depart-ment in New York City in August complaining of headacheand diplopia. His headache abruptly began one week ago,was localized to the right occipital region, and graduallymoved to his right orbit. Five days later he developed diplopia.One month prior to symptom onset, he hiked in a ruralarea of New York State, but he denied any tick bites orrash development. On presentation, our patient was hemo-dynamically stable, did not have any signs of acute infection,and denied any fevers or chills. He stated he had doublevision when opening both eyes; however if he covered his

    right eye his vision normalized. Physical examwas significantfor left sided cranial nerve 3 palsy. The rest of his physicaland neurological examinations were normal. MRI and MRAwere both negative. Syphilis serology was negative. Lumbarshowed glucose of 101, protein of 77, and 74 white bloodcells (84% lymphocytes and atypical lymphocytes). CSF wasnegative for VDRL, cryptococcal antigen, varicella zoster,HSV 1 and 2, andWest Nile virus. He had positive Lyme titersby ELISA at 6.04 (negative < 0.90) and western blot showedfive IgG and two IgM bands. He was started on acyclovirand ceftriaxone and experienced resolution of headache butcontinued to complain of diplopia. Lyme antibody inCSFwaschecked by ELISA and was reactive at 0.532 (reactive cutoff0.144). Although the CSF-to-serum ratio of IgG by Eliza wasonly 0.0880, patient was treated for oculomotor nerve palsysecondary to Lyme meningitis. Acyclovir was discontinued.He was treated with ceftriaxone for four weeks as per TheSanford Guide to Antimicrobial Therapy guidelines. Hisdiplopia resolved and he was asymptomatic two months afterinitiation of therapy.

    3. Conclusion

    This case is an example of a rare presentation of neurobor-reliosis. Although Lyme is known to affect the neurologi-cal system it usually does not manifest in the extraocularmuscles. Approximately three-fourths of patients with Lyme-associated cranial neuropathies present with a facial nerve

    HindawiCase Reports in Neurological MedicineVolume 2018, Article ID 9720843, 2 pageshttps://doi.org/10.1155/2018/9720843

    http://orcid.org/0000-0001-9678-5428https://doi.org/10.1155/2018/9720843

  • 2 Case Reports in Neurological Medicine

    palsy [1]. Lyme disease related ocular complications areuncommon, but various manifestations have been describedincluding conjunctivitis, keratitis, and extraocular musclepalsies [2]. Additionally, few cases of optic nerve papillitishave been reported [3]. Upon our review very few casesof Lyme disease affecting extraocular muscles have beenreported in literature and we were unable to find any thathighlighted that the third cranial nerve alone, as seen in ourpatient, was affected.

    4. Discussion

    Nervous system involvement occurs in up to fifteen percent ofpatients with untreated B. burgdorferi infection [4]. Patientswith early Lyme neuroborreliosis usually present in thesummer and early fall, with cranial neuropathy, particularlyseventh nerve palsy [5]. In our case the third cranial nervewas the only nerve affected. Although neuroborreliosis iscommonly associated with facial nerve palsy it may accountfor otherwise unexplained neurological manifestations andwarrants evaluation with lumbar puncture and CSF studies.Treatment with recommended antibiotics is effective in Lymeneuroborreliosis, and patients with early disease usuallyhave excellent outcomes. Recovery is slower and may beincomplete in patients with late disease [1]. Patients withunexplained symptoms and lab findings prompt furtherinvestigation of history in detail. It has been speculated thatonly about twenty-five percent of patients with Lyme diseaserecall a tick bite [6], further stressing the importance of an in-depth history and physical exam, with suspicion in patientsvisiting endemic regions. Identifying the early Lyme diseaseis vital for immediate treatment to prevent worsening andchronicity of disease.

    Conflicts of Interest

    The authors declare that there are no conflicts of interestregarding the publication of this paper.

    Authors’ Contributions

    All authors have seen and approved the manuscript andcontributed significantly to the work.

    References

    [1] J. J. Halperin, “Lyme Disease,” Continuum: Lifelong Learning inNeurology, vol. 18, no. 6, pp. 1338–1350, 2012.

    [2] A. Z. Burakgazi and C. S. Henderson, “Unusual presentation ofunilateral isolated probable lyme optic neuritis,”Case Reports inNeurological Medicine, vol. 2016, pp. 1–4, 2016.

    [3] K. McVeigh and G. Vakros, “Case report: papillitis as the soleocular sign in Lyme disease,” Clinical Ophthalmology, vol. 6, pp.1093–1097, 2012.

    [4] J. J. Halperin, “Nervous System Lyme Disease,” Clinics inLaboratory Medicine, vol. 35, no. 4, pp. 779–795, 2015.

    [5] A. R. Marques, “Lyme Neuroborreliosis,” CONTINUUM: Life-long Learning in Neurology, vol. 21, no. 6, pp. 1729–1744, 2015.

    [6] H. Raja, M. R. Starr, and S. J. Bakri, “Ocular manifestations oftick-borne diseases,” Survey of Ophthalmology, vol. 61, no. 6, pp.726–744, 2016.

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