Source:http://linkedlifedata.com/resource/pubmed/id/10617810
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2000-1-28
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pubmed:abstractText |
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma of children. Tumors arising in the extrahepatic biliary tree are extremely rare (less than 1% of cases). In this location, most are RMS of the botryoid type. We report a case of a 10-year-old child with embryonal RMS arising in the mesenchyma of the hepatic pedicle. Most tumor cells were large, round with abundant eosinophilic cytoplasm. A few cells were small round or spindle-shaped. Tumor cells showed positive immunostaining for muscle markers: desmin and sarcomeric actin. Electron microscopy revealed 2 types of cells: some were undifferentiated and others showed striated muscle differentiation features.
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pubmed:commentsCorrections | |
pubmed:language |
fre
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0242-6498
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
521-4
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pubmed:dateRevised |
2009-12-17
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pubmed:meshHeading | |
pubmed:year |
1999
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pubmed:articleTitle |
[Unusual site of an embryonal rhabdomyosarcoma of the mesenchymal hepatic pedicle].
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pubmed:affiliation |
Anatomie et Cytologie Pathologiques, CHU de Bicêtre, Le Kremlin-Bicêtre.
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
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