| Autor: |
Porto GBF; Departments of1Neurosurgery and., Welsh CT; 2Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston; and., Chaudry MI; 3Department of Neuroradiology and Neuroendovascular Surgery, Greenville Memorial Hospital, Greenville, South Carolina., Eskandari R; Departments of1Neurosurgery and. |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of neurosurgery. Pediatrics [J Neurosurg Pediatr] 2020 May 08; Vol. 26 (2), pp. 145-149. Date of Electronic Publication: 2020 May 08 (Print Publication: 2020). |
| DOI: |
10.3171/2020.3.PEDS2045 |
| Abstrakt: |
Cystic angiomatosis is a rare bone condition with complex presentation and difficult treatment. Current management strategies have poorly tolerated side effects and a low likelihood of disease eradication. The control of calvarial lesions that are symptomatic usually involves surgical excision and subsequent cranioplasty. This paradigm can present with a risk of morbidity and mortality depending on the anatomy of the lesion. Here, the authors present a novel approach to a difficult-to-treat occipital calvarial lesion directly overlying the transverse sinus, performing a small, partial-thickness craniectomy and alcohol sclerotherapy in a combined neurosurgery-neuroendovascular approach. At 3 years after treatment, the authors noted a complete, encouraging radiographic and clinical outcome. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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