Source:http://linkedlifedata.com/resource/pubmed/id/15390294
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2004-10-7
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pubmed:abstractText |
A child with an unusual association of cancers is described. The patient first presented with a rhabdomyosarcoma of the right scapular muscle, and was successfully treated with chemotherapy. Six years after diagnosis of the first malignancy, the child presented with two synchronous malignancies: osteosarcoma of the jaw and adrenocortical carcinoma. Genetic mutation analysis was performed and revealed a germline p53 mutation of CGT > CAT at codon 273. The family history was negative for any other cancer consistent with the Li-Fraumeni syndrome. This case highlights the need for close surveillance of patients with p53 mutation for malignancy and describes the occurrence of two malignancies synchronously.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1545-5009
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pubmed:author | |
pubmed:copyrightInfo |
(c) 2004 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
683-6
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pubmed:dateRevised |
2009-1-12
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pubmed:meshHeading |
pubmed-meshheading:15390294-Adrenal Cortex Neoplasms,
pubmed-meshheading:15390294-Child,
pubmed-meshheading:15390294-Follow-Up Studies,
pubmed-meshheading:15390294-Germ-Line Mutation,
pubmed-meshheading:15390294-Humans,
pubmed-meshheading:15390294-Infant,
pubmed-meshheading:15390294-Magnetic Resonance Imaging,
pubmed-meshheading:15390294-Osteosarcoma,
pubmed-meshheading:15390294-Rhabdomyosarcoma,
pubmed-meshheading:15390294-Tomography Scanners, X-Ray Computed,
pubmed-meshheading:15390294-Tumor Suppressor Protein p53
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pubmed:year |
2004
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pubmed:articleTitle |
Rhabdomyosarcoma, osteosarcoma, and adrenocortical carcinoma in a child with a germline p53 mutation.
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pubmed:affiliation |
Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
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pubmed:publicationType |
Journal Article,
Case Reports
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