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脑膜周围神经鞘瘤:一种以前未被认识到的中枢神经系统部位的良性周围神经鞘瘤,类似于脑膜瘤。

Meningial perineurioma: a benign peripheral nerve sheath tumor in a previously unrecognized central nervous system location, mimicking meningioma.

机构信息

Neuropathology Service, Institute of Pathology, University of Bern, Switzerland.

出版信息

Pathol Res Pract. 2011 Sep 15;207(9):592-6. doi: 10.1016/j.prp.2011.07.003. Epub 2011 Aug 9.

Abstract

Perineurioma is an uncommon, mostly benign, spindle-cell tumor of peripheral nerve sheath origin with a predilection for the soft tissues. Although increasing awareness points to the sites of involvement by perineurioma possibly being as ubiquitous as those frequented by schwannian tumors, only one intracerebral example has been described to date. We report on a surgically resected perineurioma of the falx cerebri in an 86-year-old woman. Preoperative imaging showed an enhancing extraaxial mass of 6 cm × 5.7 cm × 3.7 cm. Histologically, the tumor consisted of a proliferation of spindle cells interwoven by a lattice of basal lamina. Alongside a prevailing soft tissue perineurioma pattern, sclerosing and reticular areas were seen as well. Tumor cells coexpressed EMA and GLUT-1, and a minority immunoreacted for smooth muscle actin. Pericellular basal lamina was decorated with collagen type IV. No staining for S100 protein was detected. Mitotic activity was virtually absent, and the MIB1 labeling index averaged 2%. Ultrastructural examination revealed abundant pinocytotic vesicles within and conspicuous tight junctions between slender cytoplasmic processes which, in turn, were encased by discontinuous basal lamina. FISH analysis confirmed loss of at least part of one chromosome 22q. This observation calls attention to perineurioma as a novel item in the repertoire of low-grade meningial spindle cell neoplasms, in the differential diagnostic context of which it is apt to being misconstrued as either meningioma, solitary fibrous tumor, or neurofibroma. Confusion with the latter bears the risk of overgrading innocuous features of perineurioma as criteria for malignancy.

摘要

神经鞘瘤是一种罕见的、主要为良性的、起源于周围神经鞘的梭形细胞肿瘤,倾向于发生在软组织中。尽管人们对神经鞘瘤的受累部位的认识不断提高,认为其可能与雪旺细胞瘤一样无处不在,但迄今为止仅描述了一例颅内神经鞘瘤。我们报告了一例 86 岁女性大脑镰的神经鞘瘤。术前影像学显示 6cm×5.7cm×3.7cm 的增强性外轴肿块。组织学上,肿瘤由梭形细胞增生组成,由基底层的晶格交织而成。除了普遍存在的软组织神经鞘瘤模式外,还可见硬化和网状区域。肿瘤细胞共表达 EMA 和 GLUT-1,少数细胞对平滑肌肌动蛋白呈免疫反应。细胞周围基底层被 IV 型胶原修饰。未检测到 S100 蛋白染色。有丝分裂活性几乎不存在,MIB1 标记指数平均为 2%。超微结构检查显示在细长的细胞质突起内有丰富的胞饮小泡,并且在这些突起之间有明显的紧密连接,这些突起反过来又被不连续的基底层包裹。FISH 分析证实至少部分 22q 染色体缺失。这一观察结果提醒人们注意神经鞘瘤作为低级别脑膜梭形细胞肿瘤谱中的一个新成员,在鉴别诊断中,它很容易被误诊为脑膜瘤、孤立性纤维肿瘤或神经纤维瘤。与后者混淆有可能将神经鞘瘤的良性特征误认为恶性标准而过度分级。

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