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Multimodal treatment of Kasabach-Merritt syndrome arising from tufted angioma: A case report
Kasabach-Merritt syndrome (KMS) is a rare type of vascular tumor associated with a severely decreased platelet count. No standard guidelines for the treatment of the disease have been established so far. In the present study, a 1-year-old pediatric patient with KMS arising from tufted angioma was su...
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| Vydáno v: | Oncol Lett |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
D.A. Spandidos
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5453004/ https://ncbi.nlm.nih.gov/pubmed/28599491 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2017.6064 |
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