Source:http://linkedlifedata.com/resource/pubmed/id/19589466
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2009-7-10
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pubmed:abstractText |
A reversible splenial lesion of the corpus callosum has been recognized in patients with mild encephalitis/encephalopathy associated with various infectious diseases. All reported cases of encephalitis/encephalopathy, by definition, present with neurologic signs, many of which involve seizures or mildly altered states of consciousness, such as drowsiness. We report an 8-year-old boy with influenza A infection not associated with neurologic signs, whose brain magnetic resonance images incidentally revealed a reversible splenial lesion in the corpus callosum. This case indicates that a transient splenial lesion in the corpus callosum may occur during a febrile illness, without neurologic manifestations. Therefore, physicians should not diagnose or treat a patient as encephalopathic merely because of the presence of a splenial lesion on magnetic resonance imaging.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1873-5150
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
41
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
143-5
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pubmed:meshHeading |
pubmed-meshheading:19589466-Child,
pubmed-meshheading:19589466-Corpus Callosum,
pubmed-meshheading:19589466-Diagnosis, Differential,
pubmed-meshheading:19589466-Encephalitis, Viral,
pubmed-meshheading:19589466-Humans,
pubmed-meshheading:19589466-Influenza, Human,
pubmed-meshheading:19589466-Influenza A virus,
pubmed-meshheading:19589466-Magnetic Resonance Imaging,
pubmed-meshheading:19589466-Male,
pubmed-meshheading:19589466-Treatment Outcome
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pubmed:year |
2009
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pubmed:articleTitle |
Is a reversible splenial lesion a sign of encephalopathy?
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pubmed:affiliation |
Department of Pediatrics, Kobe City Medical Center General Hospital, Kobe, Japan. mtsujimd@ybb.ne.jp
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pubmed:publicationType |
Journal Article,
Case Reports
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