卡铂、依托泊苷和拉洛特替尼治疗NTRK融合阳性先天性脊髓胶质母细胞瘤

G. Vallis
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引用次数: 0

摘要

原发性脊髓多形性胶质母细胞瘤(GBM)是一种罕见的中枢神经系统肿瘤,占小儿中枢神经系统肿瘤的不到3%。这种恶性肿瘤的先天性形式更为罕见。在这里,我们报告了一个新生儿在出生时被诊断为晚期脊髓先天性胶质母细胞瘤,并成功地用依托泊苷/卡铂化疗和larorectinib治疗。病例描述患者因胎动减少,经阴道引产足月出生。她在产房时声调有所下降,右臂摆出姿势;脑部及脊柱MRI显示…浸润性肿块。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NTRK Fusion-Positive Congenital Spinal Glioblastoma treated with Carboplatin, Etoposide, and Larotrectinib
Introduction Primary spinal glioblastoma multiforme (GBM) is a rare central nervous system tumor accounting for less than 3% of pediatric central nervous system tumors. The congenital form of this malignancy is even more unusual. Here we present a case of a newborn diagnosed at birth with an advanced spinal cord congenital glioblastoma and successfully treated with etoposide/carboplatin chemotherapy and Larotrectinib. Case Description The patient was born full term via induced vaginal delivery due to decreased fetal movement. She was noted to have decreased tone in the delivery room, with a postured right arm; MRI of the brain and spine revealed an infiltrative mass in …
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