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Embryonal tumor with multilayered rosettes C19MC-altered: Report of an extremely rare malignant pediatric central nervous system neoplasm

机译:带有多层花环的胚性肿瘤经C19MC改变:极罕见的恶性小儿中枢神经系统肿瘤报告

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摘要

The 2016 update of the WHO Classification of Tumours of the Central Nervous System has redefined a number of tumors. Embryonal tumor with multilayered rosettes, C19MC-altered is one such tumor entity which has been newly defined on the basis of a characteristic molecular alteration. We report, to our knowledge, the first case of this rare pediatric brain neoplasm in the Pakistani population. An 8-month-old girl was presented with vomiting and left-sided ptosis, and magnetic resonance imaging scan showed a cerebellar tumor. Histologically, a highly cellular population of primitive cells was seen alternating with hypocellular neuropil-rich regions containing multilayered true rosettes and cells with glial and neuronal differentiation. Amplification of 19q13. 42 chromosome region on fluorescence in situ hybridization analysis confirmed the diagnosis. Post-operative radiological examination revealed widespread central nervous system involvement. Adjuvant treatment was not offered due to complications. Patient expired a week after diagnosis.
机译:世卫组织中枢神经系统肿瘤分类的2016年更新重新定义了许多肿瘤。 C19MC改变的具有多层玫瑰花结的胚状肿瘤就是这样一种肿瘤实体,它是根据特征性分子改变重新定义的。据我们所知,这是巴基斯坦人口中首例这种罕见的小儿脑肿瘤病例。一个8个月大的女孩出现呕吐和左侧上睑下垂,磁共振成像扫描显示小脑肿瘤。从组织学上看,高细胞原始细胞群与含有多层真花环的低细胞神经绒毛丰富区域以及具有神经胶质和神经元分化的细胞交替出现。 19q13的扩增。对42个染色体区域的荧光原位杂交分析证实了诊断。术后放射学检查发现广泛的中枢神经系统受累。由于并发症,未提供辅助治疗。患者在诊断后一周死亡。

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