位于儿童小脑的原发性中枢神经系统淋巴母细胞 B 细胞淋巴瘤:病例报告和文献综述。

IF 1.9 4区 医学 Q2 PEDIATRICS
Pediatric Investigation Pub Date : 2021-12-13 eCollection Date: 2021-12-01 DOI:10.1002/ped4.12303
Xueliang Yang, Yanlong Duan, Chunju Zhou, Ling Jin, Ningning Zhang, Shuang Huang, Meng Zhang, Jing Yang, Yonghong Zhang
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引用次数: 0

摘要

简介原发性中枢神经系统淋巴瘤(PCNSL)在儿童中极为罕见。我们报告了一例 3 岁女孩的 PCNSL 病例,并回顾了过去 30 年的文献:一名 3 岁女童出现步态障碍。脑部对比增强磁共振图像显示,左侧小脑半球有一单发肿块,并伴有脑积水和小脑扁桃体疝。手术切除后,患者被诊断为原发性中枢神经系统淋巴母细胞 B 细胞淋巴瘤。随后,患者接受了常规化疗,包括 6 个周期的大剂量甲氨蝶呤(HD-MTX)化疗。确诊 15 个月后,患者仍然存活,没有活动性疾病的迹象,但出现了两次慢性硬膜下血肿,通过毛细孔引流术进行了治疗:淋巴母细胞B细胞淋巴瘤是小儿PCNSL的一种罕见组织学亚型。含有HD-MTX的化疗仍是最有效的治疗方法。手术切除肿瘤后,患者应避免头部撞击,以防出现慢性硬膜下血肿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Primary central nervous system lymphoblastic B cell lymphoma located at cerebellum in a child: A case report and literature review.

Primary central nervous system lymphoblastic B cell lymphoma located at cerebellum in a child: A case report and literature review.

Primary central nervous system lymphoblastic B cell lymphoma located at cerebellum in a child: A case report and literature review.

Primary central nervous system lymphoblastic B cell lymphoma located at cerebellum in a child: A case report and literature review.

Introduction: Primary central nervous system lymphoma (PCNSL) is extremely rare in pediatric population. We reported a case of PCNSL in a 3-year-old girl and reviewed the literature in the past three decades.

Case presentation: A 3-year-old girl presented with gait disturbance. A contrast-enhanced magnetic resonance image of the brain showed a solitary bulky mass in the left cerebellar hemisphere, hydrocephalus and cerebellar tonsillar hernia. Surgical resection was performed and the patient was diagnosed with primary central nervous system lymphoblastic B cell lymphoma. Then the patient received regular chemotherapy, including 6 cycles of chemotherapy containing high-dose methotrexate (HD-MTX). The patient remains alive 15 months after the diagnosis with no evidence of active disease, but suffered twice chronic subdural hematoma, which was treated by burr hole drainage.

Conclusion: Lymphoblastic B cell lymphoma is a rare histologic subtype of pediatric PCNSL. Chemotherapy containing HD-MTX remains the most effective treatment. The patient should avoid head impact after surgical resection of the tumor to prevent chronic subdural hematoma.

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来源期刊
Pediatric Investigation
Pediatric Investigation Medicine-Pediatrics, Perinatology and Child Health
CiteScore
3.30
自引率
0.00%
发文量
176
审稿时长
12 weeks
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