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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-4-96</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-4-12-11</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Muscle Disease</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>MRI in Childhood Dermatomyositis</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>12</month>
<year>1990</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>08</month>
<year>2016</year>
</pub-date>
<volume>4</volume>
<issue>12</issue>
<fpage>96</fpage>
<lpage>96</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1990 The Author(s)</copyright-statement>
<copyright-year>1990</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="10.1016/S0022-3476(05)80686-9" vol="117" page="546">
<article-title>Magnetic resonance imaging appearance of the muscles in childhood dermatomyositis</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The demonstration of muscle involvement using the MRI in four patients with dermatomyositis is reported from the Departments of Radiology and Pediatrics, University of Michigan Hospitals, Ann Arbor, MI.</p>
</abstract>
<kwd-group>
<kwd>Dermatomyositis</kwd>
<kwd>Intensity Ratio</kwd>
<kwd>Progressive Clinical Improvement</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The demonstration of muscle involvement using the MRI in four patients with dermatomyositis is reported from the Departments of Radiology and Pediatrics, University of Michigan Hospitals, Ann Arbor, MI. Ages ranged from 4&#x00BD; to 18 years (median 8 years). The affected muscles had increased signal intensity on the T2 weighted images and normal appearance on the T1 weighted sequence. The mean intensity ratio for the patients with dermatomyositis differed significantly from that of four normal control children. Muscle groups with higher intensity ratios had lower scores on functional testing. Follow-up MRI scans demonstrated normal findings after treatment, coincident with progressive clinical improvement. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p><underline>COMMENT</underline>. The authors concluded that the MRI may be useful in the evaluation of dermatomyositis in children because it 1) is noninvasive, 2) has clear signal changes in affected muscle, 3) shows positive results at an early stage, 4) is a guide for biopsy, and 5) may assist in monitoring of the disease progress. The MRI appearances of muscles affected by hypotonic syndromes and muscular dystrophies differ from those of muscles affected by dermatomyositis. Ultrasound has been used in the diagnosis of patients with muscular dystrophy.</p>
</disp-quote>
</body>
<back>
<ref-list>
<ref id="CIT0001">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Hernandez</surname>
<given-names>RJ</given-names>
</name>
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<surname>Keim</surname>
<given-names>DR</given-names>
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<article-title>Magnetic resonance imaging appearance of the muscles in childhood dermatomyositis</article-title>
<source>J Pediatr</source>
<year>1990</year>
<month>Oct</month>
<volume>117</volume>
<issue>4</issue>
<fpage>546</fpage>
<lpage>50</lpage>
<pub-id pub-id-type="doi">10.1016/S0022-3476(05)80686-9</pub-id>
<pub-id pub-id-type="pmid">2213376</pub-id>
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</ref-list>
</back>
</article>