| pubmed-article:20870869 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20870869 | lifeskim:mentions | umls-concept:C0001554 | lld:lifeskim |
| pubmed-article:20870869 | lifeskim:mentions | umls-concept:C0011900 | lld:lifeskim |
| pubmed-article:20870869 | lifeskim:mentions | umls-concept:C0265950 | lld:lifeskim |
| pubmed-article:20870869 | lifeskim:mentions | umls-concept:C1273870 | lld:lifeskim |
| pubmed-article:20870869 | lifeskim:mentions | umls-concept:C1519814 | lld:lifeskim |
| pubmed-article:20870869 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:20870869 | pubmed:dateCreated | 2010-9-27 | lld:pubmed |
| pubmed-article:20870869 | pubmed:abstractText | The aim of this review was to discuss the current knowledge on aetiopathogenesis, diagnosis and therapeutic management of venous malformations (VMs). VMs are slow-flow vascular anomalies. They are simple, sporadic or familial (cutaneomucosal VMs or glomuvenous malformations), combined (e.g. capillaro-venous and capillaro-lymphaticovenous malformations) or syndromic (Klippel-Trenaunay, blue rubber bleb naevus and Maffucci). Genetic studies have identified causes of familial forms and of 40% of sporadic VMs. Another diagnostic advancement is the identification of elevated D-dimer level as the first biomarker of VMs within vascular anomalies. Those associated with pain are often responsive to low-molecular-weight heparin, which should also be used to avoid disseminated intravascular coagulopathy secondary to intervention, especially if fibrinogen level is low. Finally, development of a modified sclerosing agent, ethylcellulose-ethanol, has improved therapy. It is efficient and safe, and widens indications for sclerotherapy to sensitive and dangerous areas such as hands, feet and periocular area. | lld:pubmed |
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| pubmed-article:20870869 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20870869 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20870869 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:20870869 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20870869 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:20870869 | pubmed:issn | 1758-1125 | lld:pubmed |
| pubmed-article:20870869 | pubmed:author | pubmed-author:DompmartinAA | lld:pubmed |
| pubmed-article:20870869 | pubmed:author | pubmed-author:VikkulaMM | lld:pubmed |
| pubmed-article:20870869 | pubmed:author | pubmed-author:BoonL MLM | lld:pubmed |
| pubmed-article:20870869 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20870869 | pubmed:volume | 25 | lld:pubmed |
| pubmed-article:20870869 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20870869 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20870869 | pubmed:pagination | 224-35 | lld:pubmed |
| pubmed-article:20870869 | pubmed:dateRevised | 2011-11-10 | lld:pubmed |
| pubmed-article:20870869 | pubmed:meshHeading | pubmed-meshheading:20870869... | lld:pubmed |
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