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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1996-6-21
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pubmed:abstractText |
Alveolar rhabdomyosarcoma is an aggressive childhood tumor that exhibits muscle cell differentiation. Cytogenetically, it is characterized by t(2;13)(q35;q14); no consistent secondary abnormalities have been reported. Cytogenetic analysis of bone marrow in a case of alveolar rhabdomyosarcoma revealed t(2;13)(q35;q14) and der(16)t(1;16)(q21;q13). The present case and a review of the literature suggest that up to 11% of these tumors possess der(16)t(1;16)(q21;q13). This is similar to the incidence observed in the Ewing family of tumors, where unbalanced der(16)t(1;16) translocations, resulting in partial trisomy of 1q, are regarded as a consistent secondary cytogenetic change.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0165-4608
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
87
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
179-81
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:8625268-Child,
pubmed-meshheading:8625268-Chromosomes, Human, Pair 1,
pubmed-meshheading:8625268-Chromosomes, Human, Pair 16,
pubmed-meshheading:8625268-Humans,
pubmed-meshheading:8625268-Karyotyping,
pubmed-meshheading:8625268-Male,
pubmed-meshheading:8625268-Rhabdomyosarcoma, Alveolar,
pubmed-meshheading:8625268-Soft Tissue Neoplasms,
pubmed-meshheading:8625268-Translocation, Genetic
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pubmed:year |
1996
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pubmed:articleTitle |
der(16)t(1;16)(q21;q13) as a secondary change in alveolar rhabdomyosarcoma. A case report and review of the literature.
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pubmed:affiliation |
Section of Pediatrics, Institute of Cancer Research, Sutton, Surrey, U.K.
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pubmed:publicationType |
Journal Article,
Case Reports
|