Primary hepatic neuroblastoma in a 19-month-old child: A case report

J. Dimić, D. Škorić, A. Sretenović, S. Đuričić
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引用次数: 0

Abstract

Introduction. Neuroblastoma in solid organs other than the sympathetic nervous system is extremely rare. The most common site of neuroblastoma is the adrenal medulla. Liver neuroblastomas are usually metastatic lesions, particularly from stage 4S adrenal neuroblastoma. Patient review. We report the first case of primary hepatic high-risk neuroblastoma diagnosed in a child older than 12 months. The patient received multimodal oncology treatment, including chemotherapy, surgery, bone marrow transplantation, radiotherapy, and immunotherapy, as well as deep regional hyperthermia. Despite the timely diagnosis, the tumor was refractory to intensive treatment, and the patient died 2.5 years after the diagnosis. Conclusion. The differential diagnosis of primary malignant liver tumors in pediatric patients should include neuro-blastoma, especially in tumors with atypical clinical presentation. The reports of similar cases in the future may contribute to better tumor biology understanding and facilitate clinical management.
19个月儿童原发性肝神经母细胞瘤1例报告
介绍。除交感神经系统外,发生于实体器官的神经母细胞瘤极为罕见。神经母细胞瘤最常见的部位是肾上腺髓质。肝神经母细胞瘤通常是转移性病变,尤其是4S期肾上腺神经母细胞瘤。病人评估。我们报告第一例原发性肝高危神经母细胞瘤诊断在儿童大于12个月。患者接受多模式肿瘤治疗,包括化疗、手术、骨髓移植、放疗、免疫治疗以及深部局部热疗。尽管诊断及时,但肿瘤难以强化治疗,患者在确诊后2.5年死亡。结论。小儿原发性肝恶性肿瘤的鉴别诊断应包括神经母细胞瘤,尤其是临床表现不典型的肿瘤。今后类似病例的报道可能有助于更好地了解肿瘤生物学,促进临床管理。
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