Source:http://linkedlifedata.com/resource/pubmed/id/15821360
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2005-4-11
|
pubmed:abstractText |
Malignant tumors arising within dysrhaphic malformations are very rare and are mostly teratomas; so far, only one rhabdomyosarcoma has been reported in this context. We report another case of a girl with lipomyelomeningocele who developed a lumbar rhabdomyosarcoma 2 years after birth and primary closure of the neural tube defect. We present clinical, radiological and pathological findings, discuss possible mechanisms of malignant transformation and review the literature.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
1016-2291
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
40
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
293-6
|
pubmed:dateRevised |
2005-11-16
|
pubmed:meshHeading |
pubmed-meshheading:15821360-Child, Preschool,
pubmed-meshheading:15821360-Female,
pubmed-meshheading:15821360-Humans,
pubmed-meshheading:15821360-Lumbar Vertebrae,
pubmed-meshheading:15821360-Meningomyelocele,
pubmed-meshheading:15821360-Rhabdomyosarcoma, Embryonal,
pubmed-meshheading:15821360-Sacrum,
pubmed-meshheading:15821360-Spinal Cord Neoplasms
|
pubmed:articleTitle |
Spinal rhabdomyosarcoma in a child with lipomyelomeningocele.
|
pubmed:affiliation |
Department of Neurosurgery, Section of Pediatric Neurosurgery, University Hospitals, Mainz, Germany. wagner@nc.klinik.uni-mainz.de
|
pubmed:publicationType |
Journal Article,
Review,
Case Reports
|