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无神经纤维瘤病的小儿患者中低级胶质瘤的自发消退

Spontaneous regression of low-grade gliomas in pediatric patients without neurofibromatosis.

作者信息

Rozen Warren Matthew, Joseph Samuel, Lo Patrick Anthony

机构信息

Department of Neurosurgery, Royal Melbourne Hospital, Parkville, Vic., Australia.

出版信息

Pediatr Neurosurg. 2008;44(4):324-8. doi: 10.1159/000134925. Epub 2008 May 27.

Abstract

OBJECTIVE

Pediatric low-grade gliomas comprise a diverse range of central nervous system tumors, sharing the usual course of a slow progression in growth. In individual cases however, the natural history can be variable, and rarely spontaneous regression has been described. This paper describes factors associated with spontaneous regression.

METHODS

A literature review was performed to identify factors associated with spontaneous regression. A unique case is described to contribute to the findings.

RESULTS

Low-grade gliomas occurring in association with neurofibromatosis are more likely to spontaneously regress. Only 14 cases of spontaneous regression of low-grade gliomas in patients without neurofibromatosis have been described, and of these, the vast majority regress in association with optic chiasm gliomas. We describe the first documented case of spontaneous regression of a temporal lobe pilocytic astrocytoma in a patient without neurofibromatosis.

CONCLUSION

Spontaneous regression of low-grade gliomas can occur for tumors in a diversity of anatomical locations, at varying ages and in both sexes. This may have implications for management. As such, spontaneous tumor regression is an important outcome to be considered for pediatric low-grade gliomas and pilocytic astrocytomas.

摘要

目的

小儿低级别胶质瘤包括多种中枢神经系统肿瘤,通常生长缓慢。然而,在个别病例中,其自然病程可能有所不同,很少有自发消退的报道。本文描述了与自发消退相关的因素。

方法

进行文献综述以确定与自发消退相关的因素。描述了一个独特病例以补充研究结果。

结果

与神经纤维瘤病相关的低级别胶质瘤更有可能自发消退。在无神经纤维瘤病的患者中,仅有14例低级别胶质瘤自发消退的病例被报道,其中绝大多数与视交叉胶质瘤相关。我们描述了首例无神经纤维瘤病患者颞叶毛细胞型星形细胞瘤自发消退的记录病例。

结论

低级别胶质瘤的自发消退可发生于不同解剖部位、不同年龄及不同性别的肿瘤。这可能对治疗有影响。因此,自发肿瘤消退是小儿低级别胶质瘤和毛细胞型星形细胞瘤需要考虑的一个重要结果。

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