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儿童巨大海绵状血管畸形的放射学特征。

Radiological features of childhood giant cavernous malformations.

机构信息

Department of Radiology, Faculty of Medicine, Hacettepe University, Sihhiye, Ankara, 06100, Turkey.

出版信息

Neuroradiology. 2011 Apr;53(4):283-9. doi: 10.1007/s00234-010-0783-5. Epub 2010 Nov 3.

Abstract

INTRODUCTION

Giant cavernous malformations (GCM) are very large, low-flow vascular malformations, which usually have atypical imaging features and are commonly misdiagnosed preoperatively as neoplasms or vascular malformations. These lesions have mostly been reported in children. As cavernomas show different features in children compared to adults, we evaluated the imaging features of pediatric GCMs in order to help in the preoperative diagnosis of these malformations.

METHODS

Brain MR studies of nine children (mean age of 4 years; 8 months-9 years) with biopsy-proven GCM were retrospectively evaluated. We defined GCMs as cavernomas of ≥4 cm. Lesions were evaluated regarding their size, location, signal characteristics, general appearance (uni/multilocular) as well as regarding the presence of mass effect, edema, and fluid-fluid levels and were classified according to the Mottolese classification of pediatric cavernomas.

RESULTS

Lesion locations were parietal (n = 5), frontal (n = 2), temporal, and intraventricular. Seven lesions were in the periventricular region (with five in the periatrial region). Six patients had T1 hyperintense multilobulated lesions with "bubbles of blood" appearance and three patients had heterogeneous lesions with reticular core. All lesions had mass effect, edema (marked in four cases), and peripheral hemosiderin rim. Fluid-fluid levels were also common (n = 7). Most of our lesions (six of nine) were classified as type IIIA, two as type IIIC, and one as type IA.

CONCLUSION

In children, a GCM should be considered in case of very large hemorrhagic intra-axial mass with "bubbles of blood" multicystic appearance, surrounding hemosiderin ring, fluid-fluid levels, and accompanying edema-mass effect, especially in the periatrial location.

摘要

介绍

巨大海绵状血管畸形(GCM)是非常大的低流量血管畸形,通常具有非典型的影像学特征,术前常被误诊为肿瘤或血管畸形。这些病变主要发生在儿童中。由于儿童海绵状血管瘤与成人表现不同,因此我们评估了儿童 GCM 的影像学特征,以帮助术前诊断这些畸形。

方法

回顾性分析 9 例经活检证实的 GCM 患儿(平均年龄 4 岁;8 个月至 9 岁)的脑磁共振研究。我们将 GCM 定义为≥4cm 的海绵状血管瘤。评估病变的大小、位置、信号特征、一般外观(单房/多房)以及是否存在肿块效应、水肿、液-液平面,并根据儿童海绵状血管瘤的 Mottolese 分类进行分类。

结果

病变部位为顶叶(n=5)、额叶(n=2)、颞叶和脑室。7 例病变位于脑室周围(5 例位于脑室周围)。6 例患者 T1 呈高信号多叶状病变,呈“血泡”外观,3 例患者呈混杂信号病变,核心呈网状。所有病变均有肿块效应、水肿(4 例明显)和周围含铁血黄素环。液-液平面也很常见(n=7)。我们的病变中(9 例中有 6 例)大多数为 IIIA 型,2 例为 IIIC 型,1 例为 IA 型。

结论

在儿童中,对于巨大出血性脑内肿块伴“血泡”多房外观、周围含铁血黄素环、液-液平面和伴随的水肿-肿块效应,特别是在脑室周围位置,应考虑 GCM。

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