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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2008-8-20
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pubmed:abstractText |
Osteoblastoma is a rare, bone-forming neoplasm accounting for 1% of primary bone tumors. It arises in young patients and develops in long bones and posterior elements of the spine. Osteoblastoma is characterized by interconnecting trabeculae of woven bone and rimmed by prominent osteoblasts. In the current study we characterize osteoblastoma by its demographic and anatomic prevalence. We looked at rates of recurrence as related to treatment.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1096-9098
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
98
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
179-83
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pubmed:meshHeading |
pubmed-meshheading:18561158-Adolescent,
pubmed-meshheading:18561158-Adult,
pubmed-meshheading:18561158-Aged,
pubmed-meshheading:18561158-Bone Neoplasms,
pubmed-meshheading:18561158-Child,
pubmed-meshheading:18561158-Child, Preschool,
pubmed-meshheading:18561158-Curettage,
pubmed-meshheading:18561158-Female,
pubmed-meshheading:18561158-Humans,
pubmed-meshheading:18561158-Infant,
pubmed-meshheading:18561158-Male,
pubmed-meshheading:18561158-Middle Aged,
pubmed-meshheading:18561158-Neoplasm Recurrence, Local,
pubmed-meshheading:18561158-Osteoblastoma,
pubmed-meshheading:18561158-Time Factors,
pubmed-meshheading:18561158-Treatment Outcome
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pubmed:year |
2008
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pubmed:articleTitle |
Osteoblastoma: a 30-year study of 99 cases.
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pubmed:affiliation |
Harvard Medical School, Boston, Massachusetts, USA.
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pubmed:publicationType |
Journal Article
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