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星形母细胞瘤的影像表现与病理特征分析

Astroblastoma Imaging Features and Pathologic Analysis

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目的 探讨星形母细胞瘤的影像学及病理学特征.方法 回顾性分析12例星形母细胞瘤患者的临床、影像及病理资料并总结其特征.结果 12例星形母细胞瘤均原发于幕上、脑表浅部位,边界较清楚,肿瘤最大直径范围2.0~8.2 cm,中位数5.45 cm.肿瘤呈囊性伴结节2例(1例结节位于肿瘤中央区,1例结节位于肿瘤边缘区);囊实性10例,其中实性部分多发微小囊性灶,边缘多发较大囊性灶,呈"发泡状";5例实性部分伴斑点状钙化.CT平扫实性部分密度较正常脑实质高,囊性部分呈低密度.MR平扫实性部分呈T1WI等/稍低信号、T2WI等/稍高信号,囊性部分呈T1WI低信号、T2WI高信号.增强扫描实性部分明显强化,部分囊性灶可见囊壁强化.光镜检查瘤细胞围绕小血管分布形成假菊形团或乳头状结构,细胞突起粗短,细胞核远离小血管侧分布,可见血管壁透明变性.免疫组织化学示:阳性反应 GFAP(11/12)、Vimentin(9/12)、Syn(2/12)、S-100(9/11)、Olig-2(6/10)、EMA(5/7)、CD34(1/6)、ATRX(2/5);7例低级别星形母细胞瘤Ki-67阳性指数为1%~21%,平均7.7%,5例高级别星形母细胞瘤Ki-67阳性指数分别为15%~28%,平均27.8%;其中5例行分子病理学检查示IDH1/2基因(-).结论 星形母细胞瘤是一种起源不明、罕见的神经上皮肿瘤,临床表现缺乏特异性,具有一定影像学特征,多位于幕上、脑表浅部位、体积较大、边界较清楚,囊实性多见,"发泡状"具有一定特征性,可见斑点状钙化,增强扫描实性部分明显强化,瘤周水肿较轻,但确诊仍需依靠病理检查.
Objective To explore the imaging and pathological features of astroblastoma.Methods The clinical,ima-ging and pathological data of 12 patients with astroblastoma were retrospectively analyzed and their characteristics were sum-marized.Results All the 12 cases of astroblastoma were located in the supratentorial and near the brain margin,with clear boundaries,the maximum diameter range of the tumor was 2.0-8.2 cm,and the median was 5.45 cm.There were 2 cases of cystic lumps with nodules(1 nodule was located in the central area of the mass,and 1 nodule was located in the marginal area of the mass).The remaining 10 cases of multiple intra tumoral cysts typically with bubbly appearance,there were multi-ple microcystic foci in the solid part and multiple large cystic foci at the margins;5 cases were accompanied by spot-like cal-cification.CT imaging showed hypodense lesion than normal brain parenchyma,and the cystic part showed low density.The solid part of astroblastoma showed equal or slightly lower signal on T1WI and equal or higher signal on T2WI,and the cystic part showed low signal on T1 WI and high signal on T2WI.The enhanced imaging showed markedly enhanced solid mass with some enhanced cystic wall.The distribution of tumor cells around small blood vessels to form pseudochrysanthemum-shaped clusters or papillary structures on optical microscope,with thick and short cell protrusions,and nuclei distributed away from the side of hyaluromorphosis vessels.Immunohistochemistry with positive staining:GFAP(11/12),Vimentin(9/12),Syn(2/12),S-100(9/11),Olig-2(6/10),EMA(5/7),CD34(1/6),ATRX(2/5);The positive index of Ki-67 in 7 cases of low-grade astroblastoma was 1%-21%,with average of 7.7%,and 5 cases of high-grade astroblastoma was 15%-28%,with average of 27.8%,respectively.5 molecular genetics examination showed IDH1/2(-).Conclusion Astroblastoma is a rare neuroepithelial tumor with uncertain origin,no specific in clinical symptoms while characteristic radiographic fea-tures.It is usually large,well-delineated and frequently occurs insupratentorial regions above the tentum cerebellum.On ima-ging,astroblastoma shows solid mass with cysts,punctate calcification may present.The cystic part of the mass shows a bub-bly appearance,with significantly contrast enhancing and little vasogenic edema.However,the final diagnosis still depends on the histopathological examination.

AstroblastomaImaging featuresPathological features

陈安琪、常英娟、吕秀花、唐兴

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710032 西安,空军军医大学第一附属医院放射科

星形母细胞瘤 影像学特征 病理学特征

2024

临床放射学杂志
黄石市医学科技情报所

临床放射学杂志

CSTPCD北大核心
影响因子:0.872
ISSN:1001-9324
年,卷(期):2024.43(2)
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