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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-24-59</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-24-8-3</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Infectious Disorders</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>Acute Necrotizing Encephalopathy with H1N1 Influenza a Virus Infection</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>2010</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>01</month>
<year>2016</year>
</pub-date>
<volume>24</volume>
<issue>8</issue>
<fpage>59</fpage>
<lpage>60</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2010 The Author(s)</copyright-statement>
<copyright-year>2010</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="10.1002/ana.21996" vol="68" page="111">
<article-title>Acute necrotizing encephalopathy during novel influenza A (H1N1) virus infection</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>A case of acute necrotizing encephalopathy (ANE) associated with the novel H1N1 influenza A virus is reported in a 2-year-old European girl treated at the Catholic University, Rome, Italy.</p>
</abstract>
<kwd-group>
<kwd>Acute Necrotizing Encephalopathy</kwd>
<kwd>Central Necrosis of Lesions</kwd>
<kwd>Lumbar Regions</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>A case of acute necrotizing encephalopathy (ANE) associated with the novel H1N1 influenza A virus is reported in a 2-year-old European girl treated at the Catholic University, Rome, Italy. She was admitted with recurrent seizures, fever, sore throat, and altered mental status. She had nuchal rigidity and severe opisthotonus. Nasal swab was positive for the novel swine influenza A virus (H1N1). CSF showed no pleocytosis, and PCR was negative for influenza A, cytomegalovirus, Epstein-Barr virus, varicella-zoster, and enterovirus. EEG showed generalized medium-high voltage theta-delta waves. MRI hyperintense T-2 weighted lesions were present in the midbrain, brainstem meninges, and cervical cord, and swelling of subcortical white matter of insulae, thalami, geniculate bodies, and pons tegmentum. With diagnosis of H1N1 ANE the patient received antivirals, and after exclusion of herpes virus involvement, methylprednisolone (1 mg/kg/day for 5 days) was added with definite clinical improvement. Repeat MRI with contrast after 8 days showed ring-enhancement with central necrosis of lesions, and extension of spinal cord involvement to thoracic and lumbar regions. Clinical improvement of mental status and speech occurred by 20 days, but neurologic and eye examinations showed divergent strabismus of left eye, visual field abnormalities, and unsteady gait. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. ANE is a potentially fatal subtype of influenza-associated encephalopathy, characterized by multiple, symmetrical brain lesions involving thalami, brainstem tegmentum, and cerebral white matter. The authors cite 3 previous reports of neurological complications of H1N1 virus infection, including one of fatal ANE in a 12-year-old child [<xref ref-type="bibr" rid="CIT0002">2</xref>]. Another case of fatal HIN1-associated ANE in a 7-year-old girl of Chinese descent is recently reported from Children&#x2019;s Hospital, Chattanooga, TN [<xref ref-type="bibr" rid="CIT0003">3</xref>]. Increased intracranial pressure, herniation, and brain death occurred within 4 days of onset of fever and respiratory symptoms. A further case of H1N1-associated ANE in a 3-year-old Italian girl was complicated by tonsillar herniation and hydrocephalus. Consciousness improved after shunting and treatment with acyclovir and oseltamivir but voluntary movements and speech were impaired and MRI at 40 days showed residual evidence of cavitation in cerebellar hemispheres, thalami, corpus callosum, and frontal white matter. [<xref ref-type="bibr" rid="CIT0004">4</xref>]</p>
<p>H1N1 influenza virus was complicated by acute hemorrhagic leukoencephalitis and hypoxic brain injury in a 40-year-old man who failed to respond to treatment and remained in a comatose state 2 months after onset. [<xref ref-type="bibr" rid="CIT0005">5</xref>]</p>
<p>The majority of children with pandemic H1N1 influenza-associated hospitalizations in Milwaukee, WI, April to August 2009, had uncomplicated illness. Of 75 admitted, neurological disorders included seizures in 5 (6.6%), febrile seizure in 1 (1.3%), cognitive dysfunction in 6 (8%), and neuromuscular disorder in 7 (9.3%). None had encephalopathy. [<xref ref-type="bibr" rid="CIT0006">6</xref>]</p>
<p><bold>Abnormal behavior during influenza virus infection and use of Tamiflu</bold>. In Japan, oseltamivir (Tamiflu) is prescribed at the onset of influenza infection as prophylactic therapy for encephalopathy. The media has questioned whether the treatment might trigger the behavior disorder and suicidal thoughts sometimes associated with influenza virus infection. A study of 22 children admitted to hospital with abnormal behavior in Osaka, Japan, during the 2004-2007 influenza seasons, found the behavior appeared before treatment in 13 and after medication was started in 9. Oseltamivir was continued for 3-5 days after admission. Meaningless speech and involuntary movements were most frequent (16 children), and illusions, delusions, and altered awareness occurred in 14. Fear and excitement affected 6 children. All children recovered without development of severe encephalopathy. The clinical course was similar in the pre-Tami and post-Tami groups. The researchers concluded that abnormal behavior associated with some epidemics of influenza virus is not caused by oseltamivir, but further study is needed to determine the value of this treatment in prevention of encephalopathy [<xref ref-type="bibr" rid="CIT0007">7</xref>]. Abnormal behavior complicating the presenting symptoms of influenza should warn of an impending encephalopathy.</p>
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