Source:http://linkedlifedata.com/resource/pubmed/id/18284939
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2008-5-19
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pubmed:abstractText |
Hemophilic pseudotumor is an unusual complication occurring in only 1% to 2% of patients with severe factor VIII or IX deficiency, and manifests as a progressive enlargement of hematoma by recurrent hemorrhage, often resulting in bone destruction or resorption due to the chronic pressure of osseous hemorrhage. Cranial hemophilic pseudotumors are extremely rare, with only 4 previous cases associated with mild or moderate factor XIII deficiency.
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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 |
Jun
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pubmed:issn |
0090-3019
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
647-51; discussion 651
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pubmed:meshHeading | |
pubmed:year |
2008
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pubmed:articleTitle |
Cranial hemophilic pseudotumor associated with factor IX deficiency: case report.
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pubmed:affiliation |
Department of Neurosurgery, Aomori Prefectural Central Hospital, Aomori 030-8553, Japan. tomoo49@nsg.med.tohoku.ac.jp
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pubmed:publicationType |
Journal Article,
Case Reports
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