18个月大女孩额骨巨细胞瘤1例报告。

Central European Neurosurgery Pub Date : 2010-05-01 Epub Date: 2010-01-13 DOI:10.1055/s-0029-1243200
M O Ulu, H Biceroglu, F Ozlen, B Oz, N Gazioglu
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引用次数: 7

摘要

巨细胞瘤(GCT)是一种良性的,但局部侵袭性的原发性骨肿瘤,常发生在长骨的骨骺。不到1%的gct主要累及颅骨,主要发生在蝶骨和颞骨。在儿科年龄组,这种情况极为罕见。病例报告:作者报告了一个18个月大的女孩的GCT累及额骨的处理。患者接受了广泛的手术切除病变,治疗后30个月仍无肿瘤复发的临床和放射学证据。结论:虽然罕见,但gct应作为儿科患者快速扩大的颅脑肿块病变的鉴别诊断。总的手术切除消除了辅助放疗的潜在风险。然而,考虑到这些病变的侵袭性和潜在的恶性,建议仔细的长期临床和影像学随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant cell tumor of the frontal bone in an 18-month-old girl: a case report.

Introduction: Giant cell tumors (GCT) are benign, but locally aggressive primary bone neoplasms, that frequently occur in the epiphyses of the long bones. Less than 1% of all GCTs primarily involve the skull where they are preferentially seen in the sphenoid and temporal bones. In the pediatric age group they are exceptionally rare.

Case report: The authors report the management of a GCT involving the frontal bone in an 18-month-old girl. The patient underwent wide surgical excision of the lesion and remains free of clinical and radiological evidence of tumoral recurrence thirty months after treatment.

Conclusion: Although rare, GCTs should be taken into consideration as a differential diagnosis of rapidly enlarging cranial mass lesions in pediatric patients. Gross total surgical excision eliminates the potential risks of adjuvant radiotherapy. However, considering the aggressive nature and potential malignancy of these lesions, careful long-term clinical and imaging follow-up is recommended.

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Central European Neurosurgery
Central European Neurosurgery CLINICAL NEUROLOGY-NEUROSCIENCES
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