以神经母细胞瘤临床病例为例分析儿科诊断问题

E. A. Kurmaeva, G. A. Kulakova, N. A. Solovieva, S. Y. Volgina, R. V. Ivanov
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引用次数: 0

摘要

神经母细胞瘤(NB)是一种儿童期颅外恶性实体瘤。发病高峰出现在患者出生后的第一年。50%的病例在确诊时已有转移迹象。神经母细胞瘤的临床表现多种多样;症状没有特异性,取决于肿瘤的定位。原发肿瘤和转移瘤的活组织检查可确诊。对神经母细胞瘤进行局部诊断的一种特殊方法是 123I 标记的偏碘苄基胍闪烁扫描,它可以检测原发肿瘤、区域和远处转移灶的存在。大剂量化疗、移植自体干细胞和分化剂以及使用抗 GD2 单克隆抗体的免疫疗法可以延长患者的寿命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic problems in pediatrics on the example of a clinical case of neuroblastoma
Neuroblastoma (NB) is a malignant extracranial solid tumor of childhood. The peak incidence occurs in the first year of life. In 50% of cases, the disease already has signs of metastasis at the time of diagnosis. The clinical picture in neuroblastoma is varied; the symptoms are not specific and depend on the localization. The diagnosis is confirmed by histological examination of the biopsy of the primary tumor and metastasis. A specific method for the topical diagnosis of neuroblastoma is 123I-labeled metaiodobenzylguanidine scintigraphy, which makes it possible to detect the primary tumor, the presence of regional and distant metastases. Combinations of high-dose chemotherapy and transplantation of autologous stem cells and differentiating agents, as well as immunotherapy with anti-GD2 monoclonal antibodies, can increase the life expectancy of patients.
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