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儿童期残余毛细胞型星形细胞瘤放疗13年后诱发胶质肉瘤和非典型脑膜瘤。

Induction of gliosarcoma and atypical meningioma 13 years after radiotherapy of residual pilocytic astrocytoma in childhood.

作者信息

Jager Beatrice, Schuhmann Martin U, Schober Ralf, Kortmann Rolf-Dieter, Meixensberger Juergen

机构信息

Klinik und Poliklinik fur Neurochirurgie, Universitat Leipzig, Leipzig, Deutschland.

出版信息

Pediatr Neurosurg. 2008;44(2):153-8. doi: 10.1159/000113120. Epub 2008 Jan 24.

Abstract

BACKGROUND

Malignant transformation of pilocytic astrocytomas in children is rare and often linked to previous radiotherapy.

METHODS AND RESULTS

We report a patient who underwent subtotal resection of a right temporal and insular pilocytic astrocytoma at age 8 in 1988 followed by high-dose radiation therapy. A local recurrence, grade WHO III, with signs of focal sarcomatous transformation, was subtotally resected 13 years later in 2001. A new and fast growing right frontal meningioma, grade WHO II, was removed in 2003. In 2004 a second glioma recurrence was partially resected, this time graded gliosarcoma WHO IV. The patient was treated thereafter with repeated courses of temozolomide. Another tumor mass reduction in 2005 was followed by stereotactic radiotherapy. Nevertheless, he deceased 3 months later.

CONCLUSION

Most of the reported cases of malignant transformation of pilocytic astrocytomas received radiation therapy beforehand. Irradiation-induced meningiomas in children are known to occur, however not following radiotherapy of low-grade hemispheric gliomas. The presented case illustrates why adjuvant radiotherapy of residual pilocytic astrocytoma in children is not recommended anymore. For children who underwent radiotherapy in the past, we recommend MRI surveillance on a yearly basis far beyond 10 years, even in those who seem to have achieved total remission.

摘要

背景

儿童毛细胞型星形细胞瘤的恶性转化罕见,且常与既往放疗相关。

方法与结果

我们报告一例患者,1988年8岁时接受了右侧颞叶和岛叶毛细胞型星形细胞瘤次全切除术,随后接受了高剂量放射治疗。13年后的2001年,出现局部复发,WHO III级,伴有局灶性肉瘤样转化迹象,再次进行了次全切除。2003年切除了一个新出现且生长迅速的右侧额叶WHO II级脑膜瘤。2004年,第二次胶质瘤复发,部分切除,此次为WHO IV级胶质肉瘤。此后患者接受了多次替莫唑胺疗程治疗。2005年肿瘤再次缩小,随后进行了立体定向放射治疗。然而,3个月后患者死亡。

结论

大多数报道的毛细胞型星形细胞瘤恶性转化病例之前都接受过放射治疗。已知儿童放疗可诱发脑膜瘤,但低级别半球胶质瘤放疗后不会出现这种情况。本病例说明了为何不再推荐对儿童残留毛细胞型星形细胞瘤进行辅助放疗。对于过去接受过放疗的儿童,我们建议即使那些似乎已完全缓解的儿童,也要在10年以上每年进行MRI监测。

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