首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >Intraparenchymal myofibromatosis of the brain in an adult: report of an unusual case.
【24h】

Intraparenchymal myofibromatosis of the brain in an adult: report of an unusual case.

机译:成人脑实质内肌纤维瘤病:一例罕见病例的报告。

获取原文
获取原文并翻译 | 示例
           

摘要

An unusual case of intraparenchymal myofibromatosis of the brain occurring in a 29-year-old woman is described. Preoperative CT and MRI examinations revealed two well-circumscribed nodular masses localized in the wall of the left lateral ventricle and right temporal lobe, respectively. Both masses were completely resected, and the patient remains disease-free 2 years post-surgery. Histopathologically, the lesions were characterized by stratification. From outer to inner, there was a reactive glial component, lamellated well-differentiated muscle-like cells, densely compact collagen fibers and cellular tumor with nodular and hemangiopericytoma-like patterns, respectively. The myofibroblastic nature of this tumor was verified by immunohistochemical staining and ultrastructural analysis. Intraparenchymal myofibromatosis may be confused with, and should be distinguished from, meningioma, myopericytoma, solitary fibrous tumor, leiomyoma and inflammatory myofibroblastic tumor for accurate diagnosis and optimal treatment.
机译:描述了一名29岁女性发生脑内实质性肌纤维瘤病的罕见病例。术前CT和MRI检查分别发现了两个界限清楚的结节性肿块,分别位于左心室壁和右颞叶壁。两种肿块均已完全切除,术后2年患者仍无病。在组织病理学上,病变以分层为特征。从外到内,分别有一个反应性神经胶质成分,层状分化良好的肌肉样细胞,致密的胶原纤维和具有结节样和血管周皮瘤样模式的细胞瘤。通过免疫组织化学染色和超微结构分析证实了该肿瘤的肌纤维母细胞性质。实质性肌纤维瘤病可能与脑膜瘤,肌细胞瘤,孤立性纤维瘤,平滑肌瘤和炎性肌纤维母细胞瘤相混淆,并应加以区别,以进行准确的诊断和最佳治疗。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号