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1型神经纤维瘤病患者的胶质母细胞瘤:一例病例报告及文献综述

Glioblastoma in a patient with neurofibromatosis type 1: a case report and review of the literature.

作者信息

Jeong Tae-Seok, Yee Gi-Taek

机构信息

Department of Neurosurgery, Gil Medical Center, Gachon University, Incheon, Korea.

出版信息

Brain Tumor Res Treat. 2014 Apr;2(1):36-8. doi: 10.14791/btrt.2014.2.1.36. Epub 2014 Apr 29.

DOI:10.14791/btrt.2014.2.1.36
PMID:24926470
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4049554/
Abstract

Neurofibromatosis type 1 (NF1) is an autosomal dominantly inherited familial tumor syndrome. Benign tumors such as pilocytic astrocytoma, optic glioma make up the majority of intracranial neoplasms in patients with NF1. There have only been a handful of cases in which adult glioblastoma presented with NF1. A 32-year-old male presented with headache and radiological studies showing a high grade intra-axial tumor. The patient underwent gross total surgical excision and the pathology revealed glioblastoma. After the surgery, he received concomitant chemo-radiotherapy with temozolomide and adjuvant temozolomide chemotherapy. We report a NF1 patient who developed glioblastoma and reviewed related articles.

摘要

1型神经纤维瘤病(NF1)是一种常染色体显性遗传的家族性肿瘤综合征。良性肿瘤如毛细胞型星形细胞瘤、视神经胶质瘤构成了NF1患者颅内肿瘤的大部分。仅有少数成胶质细胞瘤患者伴有NF1的病例报道。一名32岁男性因头痛就诊,影像学检查显示轴内高级别肿瘤。该患者接受了肿瘤全切手术,病理检查显示为成胶质细胞瘤。术后,他接受了替莫唑胺同步放化疗及辅助化疗。我们报告了一例发生成胶质细胞瘤的NF1患者并回顾了相关文献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b9/4049554/1ad17b5e8f3d/btrt-2-36-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b9/4049554/3363d6377a96/btrt-2-36-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b9/4049554/790bf0bc958f/btrt-2-36-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b9/4049554/1ad17b5e8f3d/btrt-2-36-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b9/4049554/3363d6377a96/btrt-2-36-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b9/4049554/790bf0bc958f/btrt-2-36-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b9/4049554/1ad17b5e8f3d/btrt-2-36-g003.jpg

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