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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1995-7-24
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pubmed:abstractText |
Chordoma is generally thought to be a locally invasive tumour of low metastatic potential. Review of the literature suggests that metastatic spread from chordoma is not an uncommon occurrence, but that the metastases are usually clinically silent. We present an unusual case where a metastasis from a sacrococcygeal chordoma produced a syndrome of lumbar root compression after resection of the primary lesion.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0009-9260
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
50
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
416-7
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:7789030-Adult,
pubmed-meshheading:7789030-Chordoma,
pubmed-meshheading:7789030-Female,
pubmed-meshheading:7789030-Humans,
pubmed-meshheading:7789030-Nerve Compression Syndromes,
pubmed-meshheading:7789030-Pelvic Neoplasms,
pubmed-meshheading:7789030-Sacrococcygeal Region,
pubmed-meshheading:7789030-Spinal Neoplasms,
pubmed-meshheading:7789030-Tomography, X-Ray Computed
|
pubmed:year |
1995
|
pubmed:articleTitle |
Case report: symptomatic metastasis from a sacrococcygeal chordoma.
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pubmed:affiliation |
Department of Diagnostic Radiology, Charing Cross Hospital, London, UK.
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pubmed:publicationType |
Journal Article,
Case Reports
|