Tariq Muhammad Usman, Ahmad Zubair, Minhas Muhammad Khurram, Memon Aisha, Mushtaq Noreen, Hawkins Cynthia
Section of Histopathology, Department of Pathology and Laboratory Medicine, The Aga Khan University, Karachi, Pakistan.
Section of Paediatric Oncology, Department of Oncology, The Aga Khan University, Karachi, Pakistan.
SAGE Open Med Case Rep. 2017 Dec 4;5:2050313X17745208. doi: 10.1177/2050313X17745208. eCollection 2017.
The 2016 update of the 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.
2016年版[具体名称未给出]对多种肿瘤进行了重新定义。具有多层菊形团且C19MC改变的胚胎性肿瘤就是这样一种基于特征性分子改变新定义的肿瘤实体。据我们所知,我们报告了巴基斯坦人群中首例这种罕见的儿童脑肿瘤病例。一名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有肿瘤。组织学上,可见高度细胞化的原始细胞群与富含细胞的神经纤维区域交替出现,这些区域包含多层真性菊形团以及具有神经胶质和神经元分化的细胞。荧光原位杂交分析显示19q13.42染色体区域扩增,从而确诊。术后放射学检查显示中枢神经系统广泛受累。由于并发症未给予辅助治疗。患者在诊断一周后死亡。