原发性颅内黏液样软骨肉瘤1例

Hayam E. Rashed, Aziza E. Abdelrahman, Wael Elmesallamy, A. Obaya
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引用次数: 2

摘要

目的:颅内骨外黏液样软骨肉瘤是一种罕见的肿瘤;到目前为止,只报告了10例病例。病例报告:我们报告了一例65岁的女性,因右侧偏瘫入院,逐渐发作,病程进展超过三周。磁共振成像(MRI)显示左侧轴内顶枕占位性病变,低密度伴环形强化,周围弥漫性水肿。患者采用声纳引导开颅术进行肿块次全切除。组织病理学和免疫组织化学评估证实了骨骼外粘液样软骨肉瘤的诊断。初次出院一个月后,患者接受放疗。术后6个月的随访检查显示患者病情恶化并死亡。结论:颅内骨外黏液样软骨肉瘤是一种罕见的恶性软骨肿瘤。病理诊断是金标准,根治是标准治疗
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Intracranial Myxoid Chondrosarcoma: A case report
Objective: Intracranial extraskeletal myxoid chondrosarcoma is a rare tumor; up to date, only ten cases have been reported. Case report: We present a case report of a 65-year-old female admitted for right side hemiplegia of gradual onset and progressive course over three weeks. Magnetic resonance imaging (MRI) revealed left intra-axial parieto-occipital space occupying lesion, hypodense with ring enhancement surrounded by diffuse edema. The patient underwent subtotal resection of the mass using sonar guided craniotomy. The histopathological and immunohistochemical evaluation confirmed a diagnosis of extraskeletal myxoid chondrosarcoma. One month after initial discharge, the patient underwent radiotherapy. A follow-up examination 6 months after surgery revealed that the patient was deteriorated and died. Conclusion: intracranial extraskeletal myxoid chondrosarcoma is a rare malignant cartilaginous tumor. Pathological diagnosis is the gold standard and radical excision is the standard treatment
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