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一例具有特征性磁共振成像表现的顶叶胚胎发育不良性神经上皮肿瘤

A case of dysembryoplastic neuroepithelial tumor of the parietal lobe with characteristic magnetic resonance imaging.

作者信息

Kimura S, Kobayashi T, Hara M

机构信息

Department of Pediatrics, Urafune Hospital of Yokohama City University, Kanagawa, Japan.

出版信息

Acta Paediatr Jpn. 1996 Apr;38(2):168-71. doi: 10.1111/j.1442-200x.1996.tb03463.x.

Abstract

The case of a 4 year old boy with a dysembryoplastic neuroepithelial tumor (DNT) of the left parietal lobe is reported. The DNT was located mainly in the cortex and showed no mass effect on magnetic resonance imaging (MRI). T1-weighted images of the DNT showed the characteristic findings of lesion hypointensity, but with a well preserved gyrus-like configuration. This lesion was isointense to the normal cortex on proton density imaging and hyperintense on T2-weighted imaging. The characteristic features on T1-weighted and proton density imaging in this patient were useful in differentiating DNT from other types of tumors. Histologic findings in DNTs, which include the presence of both glial and neuronal cells without atypia and no definite transitional zone between the adjacent disorganized cortical cell layers, suggest that DNT is not a true neoplasm but rather a dysplastic lesion. It is clinically important to differentiate this tumor both from other benign tumors and malignant tumors which have different prognoses and therapies. The distinctive MRI findings, as well as the histologic features of DNT, support the diagnosis in the clinical setting.

摘要

报告了一名4岁男孩左顶叶胚胎发育不良性神经上皮肿瘤(DNT)的病例。该DNT主要位于皮质,在磁共振成像(MRI)上未显示占位效应。DNT的T1加权图像显示出病变低信号的特征性表现,但保留了良好的脑回样形态。该病变在质子密度成像上与正常皮质等信号,在T2加权成像上呈高信号。该患者T1加权和质子密度成像的特征性表现有助于将DNT与其他类型的肿瘤区分开来。DNT的组织学表现包括存在无异型性的神经胶质细胞和神经元细胞,且相邻的紊乱皮质细胞层之间没有明确的过渡带,提示DNT不是真正的肿瘤,而是发育异常性病变。将这种肿瘤与具有不同预后和治疗方法的其他良性肿瘤和恶性肿瘤区分开来具有重要的临床意义。DNT独特的MRI表现以及组织学特征支持了临床诊断。

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