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儿童原发性镰旁软骨肉瘤。

Primary parafalcine chondrosarcoma in a child.

作者信息

Gerszten P C, Pollack I F, Hamilton R L

机构信息

Department of Neurosurgery, University of Pittsburgh School of Medicine, Children's Hospital of Pittsburgh, PA 15213, USA.

出版信息

Acta Neuropathol. 1998 Jan;95(1):111-4. doi: 10.1007/s004010050773.

Abstract

Intracranial cartilaginous tumors are rare lesions, usually arising from the skull base in older individuals. We report the case of a 12-year-old girl with a low-grade type chondrosarcoma arising from the falx cerebri. To our knowledge this is the first such case reported in a child. She was treated with gross total surgical resection followed by external beam radiation because there was evidence of dural infiltration by tumor in and around the superior sagittal sinus. The patient remains progression free 9 months after surgery.

摘要

颅内软骨肿瘤是罕见的病变,通常发生于老年个体的颅底。我们报告一例12岁女孩,患有起源于大脑镰的低级别软骨肉瘤。据我们所知,这是首例在儿童中报道的此类病例。由于在矢状窦上方及其周围有肿瘤硬脑膜浸润的证据,她接受了肿瘤全切手术,随后进行了外照射放疗。术后9个月,患者病情无进展。

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