We present the first and unique case of a rapid-growing skull hemangioma in a patient with Klippel-Trénaunay-Weber syndrome. This case report provides evidence that not all rapid-growing, osteolytic skull lesions need to have a malignant character but certainly need a histopathological verification. This material offers insight into the list of rare pathological diagnoses in an infrequent syndrome.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241322 | PMC |
http://dx.doi.org/10.1007/s00701-016-3012-0 | DOI Listing |
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