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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1996-12-20
|
| pubmed:abstractText |
Von Recklinghausen neurofibromatosis (NF1) is the most common hereditary syndrome predisposing to neoplasia. The most common symptomatic manifestation of NF1 is the plexiform neurofibroma. We describe the case of a patient with classical von Recklinghausen neurofibromatosis presenting with a giant cell tumor (GCT) of the occipital bone infiltrating a surrounding plexiform neurofibroma.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0722-5091
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
15
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
226-30
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:8836608-Adult,
pubmed-meshheading:8836608-Bone Neoplasms,
pubmed-meshheading:8836608-Giant Cell Tumor of Bone,
pubmed-meshheading:8836608-Humans,
pubmed-meshheading:8836608-Male,
pubmed-meshheading:8836608-Neoplasm Invasiveness,
pubmed-meshheading:8836608-Neurofibromatosis 1,
pubmed-meshheading:8836608-Occipital Bone
|
| pubmed:articleTitle |
Giant cell tumor of the occipital bone in a case of von Recklinghausen neurofibromatosis.
|
| pubmed:affiliation |
Department of Neuropathology, University of Tübingen, Germany.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|