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小儿听神经鞘瘤表现为快速生长且具有高增殖活性。

Pediatric acoustic schwannoma showing rapid regrowth with high proliferative activity.

作者信息

Harada K, Nishizaki T, Adachi N, Suzuki M, Ito H

机构信息

Department of Neurosurgery, Yamaguchi University School of Medicine, Kogushi, Ube, Japan.

出版信息

Childs Nerv Syst. 2000 Mar;16(3):134-7. doi: 10.1007/s003810050479.

Abstract

Acoustic schwannoma is a slow-growing tumor and usually occurs in adult patients. We report a rare pediatric case of acoustic schwannoma with high proliferative potential. A 10-year-old boy was diagnosed as having a right cerebellopontine angle tumor. The tumor was subtotally resected. Histological examination revealed a typical acoustic schwannoma with a few mitotic figures. Chromosomal analysis showed no abnormality on the long arm of chromosome 22 associated with neurofibromatosis type 2. The lesion re-grew rapidly as an acoustic schwannoma, necessitating subtotal resection on three occasions and CyberKnife radiosurgery. The immunohistochemical MIB-1 staining indices of the specimens obtained at the first, second, and third operations were 2.3%, 4.6% and 14.7%, respectively. The immunohistochemical proliferative potential of acoustic schwannoma is discussed.

摘要

听神经鞘瘤是一种生长缓慢的肿瘤,通常发生于成年患者。我们报告了一例罕见的具有高增殖潜能的儿童听神经鞘瘤病例。一名10岁男孩被诊断为右侧桥小脑角肿瘤。肿瘤行次全切除。组织学检查显示为典型的听神经鞘瘤,有少量核分裂象。染色体分析显示与2型神经纤维瘤病相关的22号染色体长臂无异常。病变迅速复发为听神经鞘瘤,需要三次次全切除及射波刀放射外科治疗。第一次、第二次和第三次手术获取标本的免疫组化MIB-1染色指数分别为2.3%、4.6%和14.7%。本文对听神经鞘瘤的免疫组化增殖潜能进行了讨论。

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