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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">JCCI</journal-id>
      <journal-title-group>
        <journal-title>Journal of Clinical Case Reports and Images</journal-title>
      </journal-title-group>
      <issn pub-type="epub">2641-5518</issn>
      <publisher>
        <publisher-name>Open Access Pub</publisher-name>
        <publisher-loc>United States</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.14302/issn.2641-5518.jcci-20-3317</article-id>
      <article-id pub-id-type="publisher-id">JCCI-20-3317</article-id>
      <article-categories>
        <subj-group>
          <subject>case-report</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Ramsay Hunt Syndrome. A Case Report</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Nicolau</surname>
            <given-names>Chafick Miguel Júnior</given-names>
          </name>
          <xref ref-type="aff" rid="idm1842016188">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Joseph</surname>
            <given-names>Bruno Bidin Brooks</given-names>
          </name>
          <xref ref-type="aff" rid="idm1842017844">2</xref>
          <xref ref-type="aff" rid="idm1842016980">*</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1842016188">
        <label>1</label>
        <addr-line>Physician. Hospital Ana Costa, Santos, São Paulo Brazil; Clínica Vila Rica, Santos, São Paulo, Brazil</addr-line>
      </aff>
      <aff id="idm1842017844">
        <label>2</label>
        <addr-line>Department of Structure and Function, UNIMES- Universidade Metropolitana de Santos, São Paulo, Brazil</addr-line>
      </aff>
      <aff id="idm1842016980">
        <label>*</label>
        <addr-line>Corresponding author</addr-line>
      </aff>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>Palaniappan</surname>
            <given-names>Ramasamy</given-names>
          </name>
          <xref ref-type="aff" rid="idm1842141324">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1842141324">
        <label>1</label>
        <addr-line>Director-Research, Sree Balaji Medical College and Hospital, Chennai,                       Tamilnadu, India.</addr-line>
      </aff>
      <author-notes>
        <corresp>Joseph Bruno Bidin Brooks, Universidade Metropolitana de Santos (UNIMES), Avenida Gen. Francisco Glicério 8, Santos, São Paulo 11045-002, Brazil. Phone/Fax: +55-13-3228-3400. Email: <email>joseph3b@gmail.com</email></corresp>
        <fn fn-type="conflict" id="idm1841343556">
          <p>The authors have declared that no competing interests exist.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub" iso-8601-date="2020-05-01">
        <day>01</day>
        <month>05</month>
        <year>2020</year>
      </pub-date>
      <volume>2</volume>
      <issue>1</issue>
      <fpage>1</fpage>
      <lpage>3</lpage>
      <history>
        <date date-type="received">
          <day>13</day>
          <month>04</month>
          <year>2020</year>
        </date>
        <date date-type="accepted">
          <day>30</day>
          <month>04</month>
          <year>2020</year>
        </date>
        <date date-type="online">
          <day>01</day>
          <month>05</month>
          <year>2020</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>© </copyright-statement>
        <copyright-year>2020</copyright-year>
        <copyright-holder>Nicolau Chafick Miguel Júnior, et al.</copyright-holder>
        <license xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <self-uri xlink:href="http://openaccesspub.org/jcci/article/1340">This article is available from http://openaccesspub.org/jcci/article/1340</self-uri>
      <abstract>
        <p>This case report describes facial nerve palsy due to Ramsay Hunt syndrome, highlighting otic vesicles, audiovestibular symptoms, and imaging considerations. Management with antivirals, corticosteroids, and supportive care is summarized. Early recognition can improve outcomes and limit sequelae.</p>
      </abstract>
      <kwd-group>
        <kwd>Ramsay Hunt syndrome</kwd>
        <kwd>Magnetic Resonance Imaging</kwd>
      </kwd-group>
      <counts>
        <fig-count count="1"/>
        <table-count count="0"/>
        <page-count count="3"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <sec id="idm1841883340" sec-type="intro">
      <title>Introduction</title>
      <p>As an human alpha herpes vírus, Varicella zoster virus (VZV), causes both varicella and varicella zoster. After a incubation period of approximately 2 weeks, viral replication starts in upper respiratory mucosa and after to skin vesicular rash. Latent infection occurs through viral access to the axons of sensory and ganglion neurons and also by axonal transport. During VZV reactivation period, vesicular eruption appears in neural path dermatome. Reactivation of VZV is most commonly found in immunodepressed patients, although, it can also be found in healthy individuals.</p>
      <p>Ramsay Hunt syndrome, also named as <italic>herpes zoster oticus</italic>, is a rare condition that occurs due to (VZV) reactivation in the geniculate ganglion of the facial nerve.and in the vestibulocochlear nerve, causing sensorineural hearing loss and facial paralysis.<xref ref-type="bibr" rid="ridm1849783764">1</xref><xref ref-type="bibr" rid="ridm1849851972">2</xref><xref ref-type="bibr" rid="ridm1849865220">3</xref><xref ref-type="bibr" rid="ridm1849643868">4</xref><xref ref-type="bibr" rid="ridm1849648548">5</xref> In the present case report an unusual presentation of varicella zoster in an immunocompetent patient is reported. </p>
    </sec>
    <sec id="idm1841883052" sec-type="methods">
      <title>Methods</title>
      <p>The report of this case was submitted and approved by Universidade Metropolitana de Santos ethics committee. The patient was evaluated in a private medical clinic, as well as, complementary exams were performed in private laboratories.</p>
    </sec>
    <sec id="idm1841882980" sec-type="cases">
      <title>Case Presentation</title>
      <p>The present case refers to a 41-year-old        caucasian man with a sudden, holocranial, severe and continuous headache that lasted two days. Right after this period, the patient experienced burning pain and the appearance of vesicles throughout the right auricle. At this moment, he also noticed a decrease in auditory acuity and the presence of tinnitus in this same side associated with gait instability and decreased facial mimicry of the right side of the face. His medical history was unremarkable. He was referred for neurological evaluation at a private clinic. During neurological             examination, right facial paralysis was found                  (House-Brackmann scale grade II).<xref ref-type="bibr" rid="ridm1849636060">6</xref></p>
      <p>Otoscopic examination revealed vesicles on the right auricle. Rinne and Weber's tests showed sensorineural hearing loss; Gait instability and Romberg sign on the right side were also found.  Hematological tests were normal except for the presence of positivity on serologic (VZV) DNA polymerase chain reaction. Brain Magnetic Resonance Imaging (MRI) was performed and it was normal. Clinical evaluation and tonal audiometry were performed in a private otorhinolaryngology clinic and showed sensorineural loss on the right auricle.            Cerebrospinal fluid analyses was not performed after the main diagnosis of Ramsay Hunt Syndrome was                     postulated. After clinical diagnosis, prednisone and valacyclovir were introduced for seven days with                  satisfactory results. The clinical evolution of the VZV treatment was satisfactory; It became evident during the treatment, the presence of mild right facial paralysis (House Brackmann scale grade II). (<xref ref-type="fig" rid="idm1850403756">Figures A-E</xref>) Vertigo and postural instability treatment, as well as for tinnitus, were carried out with clonazepam and flunarizine and presented with sub-optimal response. Therapeutic                 follow-up with varicella zoster vaccine was proposed after 1 month of clinical treatment; Motor and vertigo rehabilitation were also instituted with partial results.</p>
      <fig id="idm1850403756">
        <label>Figures A-E.</label>
        <caption>
          <title> Right Auricle varicella zoster vesicles. (A) Third day of clinical evolution (B) Seventh day of clinical evolution  (C) Tenth day of clinical evolution (D) Fifteenth day of clinical evolution (E) Right facial nerve                  paralysis- House Brackmann scale grade II.</title>
        </caption>
        <graphic xlink:href="images/image1.jpeg" mime-subtype="jpeg"/>
      </fig>
    </sec>
    <sec id="idm1841880388" sec-type="discussion">
      <title>Discussion</title>
      <p>Reactivation of VZV in the geniculate                 ganglion of the facial nerve and the vestibulocochlear nerve is a rare and uncommon condition in immunocompetent individuals.. Lumbar puncture and cerebrospinal fluid collection, although not mandatory for diagnosis, is specially recommended in cases of meningoencephalitis.<xref ref-type="bibr" rid="ridm1849632820">7</xref> The presente case, highlights Ramsay Hunt clinical evolution and treatment. Mild facial paralysis and vertigo presented incomplete remission and are in accordance with current literature.<xref ref-type="bibr" rid="ridm1849783764">1</xref><xref ref-type="bibr" rid="ridm1849851972">2</xref><xref ref-type="bibr" rid="ridm1849865220">3</xref><xref ref-type="bibr" rid="ridm1849643868">4</xref><xref ref-type="bibr" rid="ridm1849648548">5</xref></p>
    </sec>
    <sec id="idm1841882476" sec-type="conclusions">
      <title>Conclusion</title>
      <p>Ramsay Hunt syndrome is not an unusual VZV clinical manifestation and thus the case report confirms the findings described in current literature and shows vestibular and facial involvement. Attention to this clinical condition and evolution may help physicians make early and correct diagnosis.</p>
    </sec>
  </body>
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