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<front>
<journal-meta>
<journal-id journal-id-type="issn">1043-3155</journal-id>
<journal-id journal-id-type="nlm-ta">Pediatr Neurol Briefs</journal-id>
<journal-id journal-id-type="pmc">pedneurbriefs</journal-id>
<journal-id journal-id-type="iso-abbrev">Pediatr Neurol Briefs</journal-id>
<journal-title-group>
<journal-title>Pediatric Neurology Briefs</journal-title>
<abbrev-journal-title>Pediatr Neurol Briefs</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2166-6482</issn>
<issn pub-type="ppub">1043-3155</issn>
<issn-l>2166-3155</issn-l>
<publisher>
<publisher-name>Pediatric Neurology Briefs Publishers</publisher-name>
<publisher-loc>Chicago, IL, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">PNB-3-64</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-3-8-10</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>CNS Infections</subject>
</subj-group>
<subj-group subj-group-type="Discipline-v2">
<subject>Neurology</subject>
<subject>Pediatrics</subject>
<subject>Nervous System Diseases</subject>
<subject>Child Development</subject>
<subject>Brain Diseases</subject>
<subject>Neurosurgery</subject>
<subject>Child</subject>
<subject>Infant</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Lyme Disease</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-0173-7931</contrib-id>
<name>
<surname>Millichap</surname>
<given-names>J. Gordon</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="aff" rid="AF0002">2</xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
</contrib>
</contrib-group>
<aff id="AF0001">
<label>1</label>Division of Neurology, Children&#x0027;s Memorial Hospital, Chicago, IL</aff>
<aff id="AF0002">
<label>2</label>Departments of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL</aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Correspondence: Dr. J. Gordon Millichap, E-mail: <email xlink:href="jgmillichap@northwestern.edu">jgmillichap@northwestern.edu</email>
</corresp>
</author-notes>
<pub-date date-type="pub" publication-format="print">
<month>08</month>
<year>1989</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>06</month>
<year>2016</year>
</pub-date>
<volume>3</volume>
<issue>8</issue>
<fpage>64</fpage>
<lpage>64</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1989 The Author(s)</copyright-statement>
<copyright-year>1989</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This work is licensed under the <uri xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</uri>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<related-article id="R1" related-article-type="commentary-article" ext-link-type="doi" xlink:href="10.1001/archneur.1989.00520430086023" vol="46" page="790">
<article-title>Central nervous system manifestations of Lyme disease</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Six patients with central nervous system manifestations of Lyme disease are reported from the Department of Neurology, Georgetown University School of Medicine, Washington, DC.</p>
</abstract>
<kwd-group>
<kwd>Lyme Disease</kwd>
<kwd>Lymphocytic Pleocytosis</kwd>
<kwd>Meningitis-Like Symptoms</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Six patients with central nervous system manifestations of Lyme disease are reported from the Department of Neurology, Georgetown University School of Medicine, Washington, DC. Behavioral changes, ataxia, and/or weakness in bulbar or peripheral muscles developed weeks to years after the initial infection. Four patients had lymphocytic pleocytosis in the CSF and two had MRI evidence of demyelination. All patients had elevated antibody titers to B burgdorferi in serum and all were treated with high-dose intravenous penicillin. Four had recovered completely within one to three months. One patient had persistent brief episodes of vestibular neuronitis and optic neuritis 15 months after antibiotic therapy for myelitis. One patient in whom antibiotic therapy had been delayed for two years after the onset of CSF abnormalities failed to respond to repeated courses of IV penicillin and showed a progressive neurologic involvement with bilateral peripheral facial weakness, double vision, weakness of triceps, wrist and finger flexors and loss of sensation in hands and arms. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p>COMMENT. A case of latent Lyme neuroborreliosis is reported in a 17 year old boy from the University of Munich, Germany [<xref ref-type="bibr" rid="CIT0002">2</xref>]. Borrelia burgdorferi was isolated from the CSF, serum IgG antibody titers were elevated, but concurrent inflammatory signs of CSF as well as intrathecal antibody production were absent. Bilateral tinnitus was the only clinical symptom and this could not definitely be attributed to the Borrelial infection.</p>
<p>Lyme disease is the subject of Medical Progress [<xref ref-type="bibr" rid="CIT0003">3</xref>]. Lyme disease commonly begins in summer with a characteristic skin lesion, erythema migrans, accompanied by flu-like or meningitis-like symptoms. Weeks or months later the patient may have neurologic or cardiac abnormalities, migratory musculoskeletal pain or arthritis. After the first several weeks of infection almost all patients have a positive antibody response to the spirochete and serologic determinations are currently considered the most practical laboratory aid in diagnosis. The author concludes that appropriate antibiotics are usually curative but longer courses of therapy are often needed later in the illness and some patients may not respond. The fetus may be at risk in mothers treated for the disease; a pregnant woman in Europe whose erythema migrans was treated with oral antibiotics gave birth to an infant who died of Lyme encephalitis. [<xref ref-type="bibr" rid="CIT0004">4</xref>]</p>
</disp-quote>
</body>
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