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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1990-11-21
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pubmed:abstractText |
Cytogenetic studies of three rare childhood brain tumors were performed. Two children presented with pure rhabdoid tumors. The third child had a tumor composed of a mixture of rhabdoid elements with neuroepithelial, epithelial, and mesenchymal tissue - an atypical teratoid tumor. All three tumors demonstrated monosomy 22 as the only cytogenetic abnormality. The cytogenetic findings suggest that loss of a gene or genes on chromosome 22 may be involved in the initiation or progression of these malignant tumors. Further studies on additional fresh tumor specimens are warranted; however, it is possible that cytogenetic studies may be used as an additional means of diagnosing rhabdoid or atypical teratoid tumors of the brain.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0022-3085
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
73
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
710-4
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2213160-Brain Neoplasms,
pubmed-meshheading:2213160-Chromosomes, Human, Pair 22,
pubmed-meshheading:2213160-Female,
pubmed-meshheading:2213160-Humans,
pubmed-meshheading:2213160-Immunoenzyme Techniques,
pubmed-meshheading:2213160-Infant,
pubmed-meshheading:2213160-Karyotyping,
pubmed-meshheading:2213160-Male,
pubmed-meshheading:2213160-Monosomy,
pubmed-meshheading:2213160-Rhabdomyosarcoma,
pubmed-meshheading:2213160-Teratoma
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pubmed:year |
1990
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pubmed:articleTitle |
Monosomy 22 in rhabdoid or atypical tumors of the brain.
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pubmed:affiliation |
Division of Human Genetics and Molecular Biology, Children's Hospital of Philadelphia, Pennsylvania.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Case Reports
|