Source:http://linkedlifedata.com/resource/pubmed/id/20850638
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2010-9-20
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pubmed:abstractText |
Kaposiform hemangioendothelioma (KHE) is a rare, locally aggressive vascular neoplasm that mainly occurs during childhood. Although KHE may involve various organs, involvement of the choledochus has not been reported. We report a case of KHE in a 5-month-old male infant. The patient was admitted with icterus and acholic stool. Contrast computed tomography revealed a vascular tumor in the hepatic portal region causing biliary obstruction. Excision of the extrahepatic duct and hepatoportoenterostomy were performed successfully, and he has been well during 3 years of postoperative follow-up.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1531-5037
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pubmed:author |
pubmed-author:FukunagaMasaharuM,
pubmed-author:HishikiTomoroT,
pubmed-author:KambeMichiyoM,
pubmed-author:NakataniYukioY,
pubmed-author:SacchiM CMC,
pubmed-author:SaitoErikoE,
pubmed-author:SaitoTakeshiT,
pubmed-author:SatoYoshiharuY,
pubmed-author:TakenouchiAyakoA,
pubmed-author:TeruiKeitaK,
pubmed-author:YoshidaHideoH
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pubmed:copyrightInfo |
Copyright © 2010 Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1887-9
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pubmed:meshHeading |
pubmed-meshheading:20850638-Cholestasis,
pubmed-meshheading:20850638-Common Bile Duct Neoplasms,
pubmed-meshheading:20850638-Hemangioendothelioma,
pubmed-meshheading:20850638-Humans,
pubmed-meshheading:20850638-Infant,
pubmed-meshheading:20850638-Jaundice, Obstructive,
pubmed-meshheading:20850638-Male
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pubmed:year |
2010
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pubmed:articleTitle |
Kaposiform hemangioendothelioma of the choledochus.
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pubmed:affiliation |
Department of Pediatric Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8677, Japan. kta@cc.rim.or.jp
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pubmed:publicationType |
Journal Article,
Case Reports
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