小儿原发性硬膜淋巴母细胞 B 细胞淋巴瘤表现为额顶区血肿:病例报告。

IF 0.9 4区 医学 Q4 HEMATOLOGY
Ayşe Ceyda Ören, Esra Pekpak Şahinoğlu, Sibel Cangi, Mehmet Alptekin, Vezir Korkmaz, Sinan Akbayram
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引用次数: 0

摘要

原发于脑膜而未累及大脑或全身的淋巴瘤是原发性中枢神经系统淋巴瘤中极为罕见的一种。这里,我们报告了一例原发性硬脑膜淋巴瘤病例,患者是一名 3 岁男孩,因头痛、恶心和呕吐发作数日而被送往医院。脑部 CT 扫描发现右侧顶叶前部有急性血肿。患者接受了血肿清除手术,随后血肿被送去进行病理检查。病理报告显示为淋巴母细胞 B 细胞淋巴瘤,Ki-67 增殖指数为 80%。放射学和 FDG-PET/CT 成像以及骨髓检查均未发现任何系统性疾病。NHL BFM 2012淋巴细胞淋巴瘤治疗方案已经启动并顺利完成。该患者已接受了约两年的随访,目前仍然存活且没有患病。这是文献中报道的首例小儿原发性硬膜淋巴母细胞 B 细胞淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pediatric Primary Dural Lymphoblastic B-cell Lymphoma Presenting as Hematoma in the Frontoparietal Region: A Case Report.

Lymphomas originating from the meninges without brain or systemic involvement represent an extremely rare type of primary central nervous system lymphomas. Here, we report a case of primary dural lymphoma in a 3-year-old boy who was brought to the hospital due to headache, nausea, and vomiting episodes ongoing for several days. An acute hematoma in the right frontoparietal region was detected on a brain CT scan. The patient underwent surgery to remove the hematoma, which was then sent for pathologic examination. The pathology report revealed lymphoblastic B-cell lymphoma with a Ki-67 proliferation index of 80%. Radiologic and FDG-PET/CT imaging, as well as bone marrow examination, did not reveal any systemic disease. The NHL BFM 2012 lymphoblastic lymphoma treatment protocol was started and successfully completed. The patient has been followed for ~2 years and is still alive and disease-free. This is the first case of pediatric primary dural lymphoblastic B-cell lymphoma ever reported in the literature.

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来源期刊
CiteScore
1.90
自引率
8.30%
发文量
415
审稿时长
2.5 months
期刊介绍: ​Journal of Pediatric Hematology/Oncology (JPHO) reports on major advances in the diagnosis and treatment of cancer and blood diseases in children. The journal publishes original research, commentaries, historical insights, and clinical and laboratory observations.
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