Group3 Medulloblastoma with Bone Marrow and Abdominal Cavity Metastasis: A Case Report

IF 6.5 1区 医学 Q1 ONCOLOGY International Journal of Radiation Oncology Biology Physics Pub Date : 2025-03-01 Epub Date: 2025-02-03 DOI:10.1016/j.ijrobp.2024.11.061
S. Li , L. Chen , L. Wang , Y. Zhang , H. Kang , M. Ye , M. Lai , R. Al
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Abstract

Medulloblastoma is an infratentorial primitive neuro-ectodermal tumour, which is commonly occurring in childhood. It often spreads through the cerebrospinal fluid pathways with a very low rate of systemic metastases. Extra-central nervous system metastases have a poor prognosis in medulloblastoma. Here, we reported a case of Group3 medulloblastoma with bone marrow and abdominal cavity metastasis.

Methods

A 10-year-old girl complained of headache, dizziness, vomiting and nausea. Magnetic resonance imaging(MRI) of the brain showed a large mass in the fourth ventricle and obstructive hydrocephalus. The surgery was performed to remove the mass and ventriculoabdominnal shunt was performed for obstructive hydrocephalus. Histological verification was proven classic medulloblastoma and next-generation sequencing confirmed molecular group of Gruop3 with MYC amplication. Radiotherapy was subsequently performed one month after the surgery.

Results

During the radiotherapy, brain MRI showed metastasis on the surface of the brain, which confer a poor prognosis. After the radiotherapy According to the therapeutic schedule, She would accept chemotherapy one month after the radiotherapy. But She suffered severe bone marrow suppression manifested as anaemia and thrombocytopenia, which can not be improved by medication and blood transfusion. A bone marrow aspiration was subsequently performed, and bone marrow smear showed large numbers of tumor cells at high magnification and was lack of normal hematopoietic cells. The girl was deteriorating rapidly with jaundice, ascites, hepatosplenomegaly and pancreatitis after the bone marrow aspiration. We found a lot of tumor cells in the bleeding tendency ascites and finally confirmed bone marrow and abdominal cavity metastasis concurrently.

Conclusion

Eventually, She died less than a month after the metastasis and the overall survival was only 6 months. This typical case demonstrated severe bone marrow suppression of unknown origin should caused alarm and be performed bone marrow aspiration as soon as possible. The prognosis of medulloblastoma with extra-central nervous system metastases is poor and people may die in months.
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髓母细胞瘤合并骨髓及腹腔转移1例
髓母细胞瘤是一种幕下原始神经外胚层肿瘤,常见于儿童。它通常通过脑脊液途径传播,全身转移率很低。髓母细胞瘤的中枢外神经系统转移预后较差。在此,我们报告一例第3组髓母细胞瘤伴骨髓及腹腔转移。方法1例10岁女童自诉头痛、头晕、呕吐、恶心。脑磁共振成像(MRI)显示第四脑室有一个大肿块和阻塞性脑积水。手术切除肿块并对梗阻性脑积水进行脑室腹腔分流术。组织学证实为典型髓母细胞瘤,下一代测序证实了MYC扩增的Gruop3分子群。术后1个月进行放射治疗。结果放疗期间,脑MRI显示脑表面转移,预后较差。放疗后根据治疗方案,放疗后1个月接受化疗。但她患有严重的骨髓抑制,表现为贫血和血小板减少症,无法通过药物和输血改善。随后行骨髓穿刺,高倍镜下骨髓涂片显示大量肿瘤细胞,缺乏正常的造血细胞。骨髓穿刺后,女孩病情迅速恶化,出现黄疸、腹水、肝脾肿大和胰腺炎。我们在有出血倾向的腹水中发现了大量的肿瘤细胞,最终证实骨髓和腹腔同时转移。结论患者在转移后不到1个月死亡,总生存期仅为6个月。本典型病例显示骨髓严重抑制,原因不明,应引起警惕,尽早行骨髓抽吸术。髓母细胞瘤合并中枢外神经系统转移的预后很差,患者可能在几个月内死亡。
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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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