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Clinicopathological features of cerebellar lipidized medulloblastoma: a case report and review of literatures

机译:小脑脂质化髓母细胞瘤的临床病理特征:一例报道并文献复习

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Objective To explore the clinicopathological features of cerebellar lipidized medulloblastoma. Methods The clinical manifestations, neuroimaging, histopathological and immunohistochemical features were analysed in one case of lipidized medulloblastoma in the cerebellar vermis. Related literatures were reviewed. Results A 26 ? year ? old man presented with intermittent headache,accompanied by dizziness, nausea and vomiting. The magnetic resonance imaging (MRI) demonstrated a mass located the cerebellar vermis convex to the fourth ventricle. The tumor with well? demarcated boundary was homogeneous hypointense on T1 weighted and heterogeneous hyperintense on T2 weighted images, and enhanced brilliantly and homogenously on contrast. The patient subsequently underwent gross total mass resection. Microscopically,there was diffuse infiltration by high cellularity of tumor cells. The cytoplasm were thin eosinophilic to amphophilic. The neoplastic cells showed round to oval hyperchromatic nuclei with a delicately stippled chromatin and occasional conspicuous nucleoli and numerous mitotic figures were also present. Thin?wall vascular proliferation was detected. Lipid?laden cells were focally distributed in tumor tissue. On immunohistochemical examination, the neoplasm was reactive for CD56 and synaptophysin (Syn), focally positive for neurofilament protein (NF), weakly positive for oligodendrocyte lineage transcription factor 2 (Olig?2), and negtive for nestin, neuronal nuclei (NeuN), S?100 protein (S ? 100), glial fibrillary acidic protein (GFAP) and epithelial membrane antigen (EMA). TP53 protein was over expressed in 10% of tumor cells. Ki ? 67 antigen labeling index were about 40% . Conclusion Cerebellar lipidized medulloblastoma is rare. Neuroimaging showed space occupying lesion in cerebellar vermis. Histologically, the tumor cells were consisted of monotonous, round cells with focal accumulations of lipidized cells. The differential diagnosis include liponeurocytoma and ependymoma and so on. DOI:10.3969/j.issn.1672?6731.2012.03.014.
机译:目的探讨小脑脂质化髓母细胞瘤的临床病理特征。方法对1例小脑mis脂化髓母细胞瘤的临床表现,神经影像学,组织病理学和免疫组化特征进行分析。回顾了相关文献。结果A 26?年 ?老人出现间歇性头痛,伴有头晕,恶心和呕吐。磁共振成像(MRI)显示肿块位于小脑ver突向第四脑室。肿瘤好吗?划定的边界在T1加权图像上是均质的低聚点,而在T2加权图像上是异质的超强的,并且在对比度上明亮而均匀地增强。患者随后接受了总肿物切除术。镜下可见肿瘤细胞的高细胞性弥漫性浸润。细胞质是嗜酸性至两亲性。赘生性细胞显示圆形至椭圆形的增色核,染色质细腻点缀,核仁偶尔可见,并且还存在许多有丝分裂图。检测到薄壁血管增生。载脂细胞集中分布在肿瘤组织中。在免疫组织化学检查中,肿瘤对CD56和突触素(Syn)具有反应性,对神经丝蛋白(NF)呈局部阳性,对少突胶质细胞谱系转录因子2(Olig?2)呈弱阳性,对巢蛋白,神经元核(NeuN)呈阴性, S?100蛋白(S?100),神经胶质纤维酸性蛋白(GFAP)和上皮膜抗原(EMA)。 TP53蛋白在10%的肿瘤细胞中过表达。 ? 67抗原标记指数约为40%。结论小脑脂化性髓母细胞瘤少见。神经影像检查显示小脑ver部占位性病变。在组织学上,肿瘤细胞由单调的圆形细胞组成,具有脂质化细胞的局部聚集。鉴别诊断包括脂肪神经细胞瘤和室管膜瘤等。 DOI:10.3969 / j.issn.1672?6731.2012.03.014。

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