Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2013
Giant cell reparative granuloma of the pediatric cranium: case report and review of the literature.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Conley Adam, Cho Brian H, Tye Gary W, Reavey-Cantwell John, Coelho Daniel, Fuller Christine E, Rhodes Jennifer L
Аннотация
PURPOSE: Giant cell reparative granulomas are rare bone tumors. Although benign, these tumors are locally destructive and can be highly vascular. They seldom occur in the cranial vault. We describe a multidisciplinary approach to a case of giant cell reparative granuloma of the cranium in a 3-year-old patient.
CASE REPORT: A 3-year-old girl female referred to the pediatric neurosurgery department for evaluation of a retro-auricular mass. She had a history of recurrent otitis media with two subsequent courses of antibiotics without resolution. CT imaging revealed an expansive lesion located in the right mastoid region. Open surgical biopsy revealed a hemorrhagic tumor consistent with a giant cell reparative granuloma. Angiography identified a hypervascular tumor blush that was supplied by the occipital artery. Preoperative transcatheter embolization was performed followed by a multidisciplinary surgical resection and reconstruction. Blood loss was minimal, and the patient recovered well after surgery.
CONCLUSION: Preoperative endovascular embolization and a multidisciplinary intraoperative approach with primary resection and cranial vault reconstruction is an effective approach to hypervascular giant cell reparative granulomas.
CASE REPORT: A 3-year-old girl female referred to the pediatric neurosurgery department for evaluation of a retro-auricular mass. She had a history of recurrent otitis media with two subsequent courses of antibiotics without resolution. CT imaging revealed an expansive lesion located in the right mastoid region. Open surgical biopsy revealed a hemorrhagic tumor consistent with a giant cell reparative granuloma. Angiography identified a hypervascular tumor blush that was supplied by the occipital artery. Preoperative transcatheter embolization was performed followed by a multidisciplinary surgical resection and reconstruction. Blood loss was minimal, and the patient recovered well after surgery.
CONCLUSION: Preoperative endovascular embolization and a multidisciplinary intraoperative approach with primary resection and cranial vault reconstruction is an effective approach to hypervascular giant cell reparative granulomas.
Предметные рубрики MeSH
BiopsyCerebral AngiographyChild, PreschoolDiagnosis, DifferentialEmbolization, TherapeuticFemaleGranuloma, Giant CellHumansMagnetic Resonance ImagingNeurosurgical ProceduresPatient Care PlanningPatient Care TeamPostoperative ComplicationsRisk Reduction BehaviorSkullSkull NeoplasmsTomography, X-Ray ComputedTreatment Outcome