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Kaposiform hemangioendothelioma arising from the internal auditory canal
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chang, J M | - |
dc.contributor.author | Kwon, B J | - |
dc.contributor.author | Han, M H | - |
dc.contributor.author | Kang, H S | - |
dc.contributor.author | Chang, K H | - |
dc.date.accessioned | 2009-10-05T03:18:06Z | - |
dc.date.available | 2009-10-05T03:18:06Z | - |
dc.date.issued | 2006 | - |
dc.identifier.citation | AJNR Am J Neuroradiol 2006;27:931-33 | en |
dc.identifier.issn | 0195-6108 | - |
dc.identifier.uri | https://hdl.handle.net/10371/10062 | - |
dc.description.abstract | Kaposiform hemangioendothelioma is a rare vascular tumor and locally aggressive endothelial-derived spindle cell neoplasm, which occurs almost exclusively in infants and adolescents. Radiologically, hemangioendothelioma, including Kaposiform hemangioendothelioma, is seen as a highly vascularized well-enhancing tumor, but no characteristic findings differentiate Kaposiform hemangioendothelioma from other soft-tissue tumors, particularly when the tumor is too small to have any locally aggressive features or identifiable large vessels. We present a case of Kaposiform hemangioendothelioma in the internal auditory canal that had no differential features on initial MR images and rapidly grew into a huge mass in a few months. | en |
dc.language.iso | en | - |
dc.publisher | American Society of Neuroradiology | en |
dc.title | Kaposiform hemangioendothelioma arising from the internal auditory canal | en |
dc.type | Article | en |
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