Source:http://linkedlifedata.com/resource/pubmed/id/15163230
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2004-5-27
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pubmed:abstractText |
We describe the case of a 31-week fetus who died in utero with an invasive retroperitoneal kaposiform hemangioendothelioma. This rare vascular neoplasm usually presents as a localized violaceous skin lesion in infants and behaves in a benign fashion; however, kaposiform hemangioendothelioma may present as an invasive neoplasm of the chest or abdominal cavity, where it can lead to the Kasabach-Merritt syndrome, which consists of thrombocytopenia, consumptive coagulopathy, and microangiopathic anemia in association with a vascular anomaly. The case we describe is unique in that the tumor presented in utero and led to intrauterine nonimmune fetal hydrops. Kaposiform hemangioendothelioma has been described in utero; however, to our knowledge, intrauterine fetal death as a direct consequence has not been reported previously in the literature.
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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 |
Jun
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pubmed:issn |
1543-2165
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
128
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
678-81
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:15163230-Female,
pubmed-meshheading:15163230-Fetal Death,
pubmed-meshheading:15163230-Fetal Diseases,
pubmed-meshheading:15163230-Hemangioendothelioma,
pubmed-meshheading:15163230-Humans,
pubmed-meshheading:15163230-Hydrops Fetalis,
pubmed-meshheading:15163230-Neoplasm Invasiveness,
pubmed-meshheading:15163230-Pregnancy,
pubmed-meshheading:15163230-Retroperitoneal Neoplasms
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pubmed:year |
2004
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pubmed:articleTitle |
Kaposiform hemangioendothelioma associated with nonimmune fetal hydrops.
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pubmed:affiliation |
Arkadi M. Rywlin MD Department of Pathology and Laboratory Medicine, Mount Sinai Medical Center, Miami Beach, Fla 33140, USA. amartin2@msmc.com
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pubmed:publicationType |
Journal Article,
Case Reports
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