ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2023
Kaposiform hemangioendothelioma of skull base with dura invasion in a pediatric patient: a case report.
Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed, 3 citations in OpenAlex.
- Dural composite hemangioendothelioma: The first intracranial case.Surgical neurology international · 2024Article
- Diagnosis and differentiation of Kaposiform hemangioendothelioma based on ultrasound radiomics.American journal of cancer research · 2024Article
- Case Report: Recurrent blepharal kaposiform hemangioendothelioma in an adult patient.Frontiers in surgery · 2023Article
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6 authors at 2 institutions in 1 country.
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Abstract
Kaposiform hemangioendothelioma is an extremely rare vascular tumor which shows aggressive local growth. We present a case of rapid growing vascular skull tumor with dura invasion in a pediatric patient with neurofibromatosis type 1. A 14-year-old male complained of headache and dizziness for 1 month after minor head trauma. Brain magnetic resonance imaging (MRI) revealed a 5-cm-sized tumor in the left frontotemporal bone with internal hemorrhage and cystic changes. The gross total resection of tumor was done. At the 7-month follow-up, brain MRI revealed a recurrent skull tumor with intracranial dura mass. He underwent second surgery, and the pathologic diagnosis was suggestive of Kaposiform hemangioendothelioma. For this vascular proliferative tumor, mTOR inhibitor was treated for 6 months, and there was the recurred nodular-enhancing mass along the sphenoid ridge. After additional 2 months of medication, the following MRI revealed a decreased nodular-enhancing mass.
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