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伴有颗粒细胞分化的髓内星形细胞瘤。

Intramedullary astrocytoma with granular cell differentiation.

作者信息

Rodriguez y Baena R, Di Ieva A, Colombo P, Collini P, Navarria P, Scorsetti M, Gaetani P, Santoro A

机构信息

Department of Neurosurgery, Istituto Clinico Humanitas, IRCCS, Via Manzoni, 56, 20089 Rozzano, Milan, Italy.

出版信息

Neurosurg Rev. 2007 Oct;30(4):339-43; discussion 343. doi: 10.1007/s10143-007-0079-3. Epub 2007 May 5.

Abstract

Granular cell astrocytomas are uncommon tumors of the central nervous system (CNS) of which no cases have been documented in the spinal cord. This variant of glioma should not be confused with benign granular cell tumor which, although rare, has been well characterized in the spinal cord. We describe here the clinical, pathological, and radiological features of such an astrocytoma arising within the spinal cord at the dorsal level. A 48-year-old female was seen after about 1 year of dorsal pain and gradual spastic paraparesis. Magnetic resonance imaging (MRI) studies showed a 2-cm contrast-enhanced mass in the spinal cord at T6-T7, which had the appearance of an astrocytoma. At surgery, the tumor was found to be infiltrating a posterior column with no dural attachment. It was debulked and dissected. The histological diagnosis was astrocytoma with granular cell differentiation. In addition to documenting a unique example of intramedullary granular cell astrocytoma, we review the literature to investigate differences from other tumors with granular changes described in the spinal cord.

摘要

颗粒细胞型星形细胞瘤是中枢神经系统(CNS)的罕见肿瘤,脊髓中尚无病例记录。这种胶质瘤变体不应与良性颗粒细胞瘤混淆,后者虽然罕见,但在脊髓中已有充分的特征描述。我们在此描述了一例发生于脊髓背侧节段的此类星形细胞瘤的临床、病理和放射学特征。一名48岁女性在出现背痛约1年并逐渐发展为痉挛性截瘫后前来就诊。磁共振成像(MRI)检查显示,在T6 - T7脊髓节段有一个2厘米的强化肿块,表现为星形细胞瘤。手术中发现肿瘤浸润后柱,无硬膜附着。对其进行了大部分切除并解剖。组织学诊断为具有颗粒细胞分化的星形细胞瘤。除了记录髓内颗粒细胞型星形细胞瘤的一个独特病例外,我们还回顾了文献,以研究其与脊髓中描述的其他具有颗粒变化的肿瘤的差异。

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