Abstract
We present the first and unique case of a rapid-growing skull hemangioma in a patient with Klippel-Tr,naunay-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.
Original language | English |
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Pages (from-to) | 397-400 |
Number of pages | 4 |
Journal | Acta Neurochirurgica |
Volume | 159 |
Issue number | 2 |
DOIs | |
Publication status | Published - Feb 2017 |
Keywords
- Klippel-Trenaunay-Weber syndrome
- Skull hemangioma
- Hemangioma
- Skull tumor
- Surgical pathology
- KLIPPEL-TRENAUNAY-SYNDROME