Cakirer S, Karaarslan E
Istanbul Sisli Etfal Hospital, Department of Radiology, Istanbul, Turkey.
Acta Radiol. 2004 Oct;45(6):669-73. doi: 10.1080/02841850410001150.
A patient with neurofibromatosis type I (NF1) was followed-up with serial magnetic resonance imaging (MRI) studies over a period of 6 years. A contrast-enhancing lesion of the internal capsule, histologically proven to be pilocytic astrocytoma through stereotactic brain biopsy with mass effect and associated edema, was detected to reveal spontaneous involution on follow-up MRI studies. Although spontaneous regression of gliomas of the optic pathway-hypothalamus in patients with NF1 is relatively common in the literature, spontaneous involution of non-optic (i.e. areas other than optic pathways and hypothalamus) gliomas is rarely reported. Conservative management with follow-up MRI studies should be considered for non-optic glial tumors and tumor-like masses in patients with NF1, and surgical treatment should not be considered unless the lesions exhibit a rapid or unrelenting growth on serial MRI studies or produce significant clinical deterioration.
对一名患有I型神经纤维瘤病(NF1)的患者进行了为期6年的系列磁共振成像(MRI)随访研究。通过立体定向脑活检组织学证实为毛细胞型星形细胞瘤的内囊强化病变,伴有占位效应和相关水肿,在随访MRI研究中显示自发消退。虽然NF1患者视路 - 下丘脑胶质瘤的自发消退在文献中相对常见,但非视路(即视路和下丘脑以外的区域)胶质瘤的自发消退很少有报道。对于NF1患者的非视路神经胶质瘤和肿瘤样肿块,应考虑采用随访MRI研究进行保守治疗,除非病变在系列MRI研究中显示快速或持续生长或导致明显的临床恶化,否则不应考虑手术治疗。