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儿童多形性黄色星形细胞瘤:磁共振成像及扩散磁共振成像特征

Pleomorphic xanthoastrocytoma of childhood: MR imaging and diffusion MR imaging features.

作者信息

Moore W, Mathis D, Gargan L, Bowers D C, Klesse L J, Margraf L, Koral K

机构信息

From the Departments of Radiology (W.M., K.K.).

Pathology (D.M., L.M.).

出版信息

AJNR Am J Neuroradiol. 2014 Nov-Dec;35(11):2192-6. doi: 10.3174/ajnr.A4011. Epub 2014 Jul 3.

Abstract

BACKGROUND AND PURPOSE

Pleomorphic xanthoastrocytomas are rare astrocytic neoplasms of childhood and young adulthood. The purpose of this retrospective review was to evaluate MR imaging features of pediatric pleomorphic xanthoastrocytomas with an emphasis on diffusion MR imaging.

MATERIALS AND METHODS

Review of the neuro-oncology data base revealed 11 pediatric patients (range, 4.7-16.1 years) with pleomorphic xanthoastroacytomas with 9 of these patients having preoperative MR imaging available. Six patients had preoperative diffusion MR imaging. Demographics, histopathology slides, conventional imaging characteristics (location, cystic component, hemorrhage, enhancement, vasogenic edema, inner table scalloping), and ADC metrics (mean tumor ADC and tumor to normal brain ADC ratio) were evaluated.

RESULTS

Three pleomorphic xanthoastrocytomas had anaplastic features. Ten tumors were supratentorial. Two-thirds (6 of 9) of all tumors were either predominantly cystic or had cystic components, and three-fourths (6 of 8) of the supratentorial tumors had associated inner table scalloping. Seven of the 9 tumors had marked vasogenic edema (>10 mm). Mean tumoral ADC (n = 7) was 912 ± 219 × 10(-6) mm(2)/s (min-max: 617-1189). The tumor to normal brain ADC ratio was 1.14 ± 0.26 (min-max: 0.75-1.47).

CONCLUSIONS

Pleomorphic xanthoastrocytoma should be entertained in the differential diagnosis of peripheral supratentorial tumors that appear during childhood. Cysts, inner table scalloping, and marked vasogenic edema are relatively frequent features. Relatively low ADC values and ADC ratios are not uncommon in pleomorphic xanthoastrocytoma.

摘要

背景与目的

多形性黄色星形细胞瘤是儿童及青年时期罕见的星形细胞肿瘤。本回顾性研究的目的是评估儿童多形性黄色星形细胞瘤的磁共振成像(MR)特征,重点关注扩散加权磁共振成像。

材料与方法

回顾神经肿瘤数据库发现11例患有多形性黄色星形细胞瘤的儿科患者(年龄范围4.7 - 16.1岁),其中9例患者有术前MR成像资料。6例患者有术前扩散加权MR成像。评估了患者的人口统计学资料、组织病理学切片、传统成像特征(位置、囊性成分、出血、强化、血管源性水肿、内板扇贝样改变)以及表观扩散系数(ADC)指标(肿瘤平均ADC值及肿瘤与正常脑ADC比值)。

结果

3例多形性黄色星形细胞瘤具有间变特征。10例肿瘤位于幕上。所有肿瘤的三分之二(9例中的6例)主要为囊性或有囊性成分,幕上肿瘤的四分之三(8例中的6例)伴有内板扇贝样改变。9例肿瘤中有7例有明显的血管源性水肿(>10 mm)。7例肿瘤的平均肿瘤ADC值为912 ± 219×10⁻⁶ mm²/s(最小值 - 最大值:617 - 1189)。肿瘤与正常脑ADC比值为1.14 ± 0.26(最小值 - 最大值:0.75 - 1.47)。

结论

在儿童期出现的幕上周围性肿瘤的鉴别诊断中应考虑多形性黄色星形细胞瘤。囊肿、内板扇贝样改变和明显的血管源性水肿是相对常见的特征。多形性黄色星形细胞瘤中相对较低的ADC值和ADC比值并不少见。

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