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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
1996-12-13
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pubmed:abstractText |
A young child was admitted with a cauda equina syndrome believed to be progressive, but unrelated to a congenital anomaly. Magnetic resonance imaging studies revealed the presence of an intradural tumor in the cauda equina. A yellow pasty tumor with nerve root infiltration was identified at surgery. Histologic features were pathognomonic for histiocytosis X. The patient's management and review of the literature are discussed.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0887-8994
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
14
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
231-5
|
pubmed:dateRevised |
2006-5-23
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pubmed:meshHeading |
pubmed-meshheading:8736408-Cauda Equina,
pubmed-meshheading:8736408-Child, Preschool,
pubmed-meshheading:8736408-Histiocytosis, Langerhans-Cell,
pubmed-meshheading:8736408-Humans,
pubmed-meshheading:8736408-Magnetic Resonance Imaging,
pubmed-meshheading:8736408-Male,
pubmed-meshheading:8736408-Nerve Compression Syndromes
|
pubmed:year |
1996
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pubmed:articleTitle |
Cauda equina histiocytosis X.
|
pubmed:affiliation |
Department of Neurosurgery, Montreal Children's Hospital, Quebec, Canada.
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pubmed:publicationType |
Journal Article,
Review,
Case Reports
|