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Intramedullary metastasis in medulloblastoma: a case report and literature review

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Abstract

Background

Cerebellar medulloblastomas are the most common malignant tumors of the posterior fossa in childhood that frequently metastasize. Leptomeningeal dissemination and distant metastasis have been associated with medulloblastomas; however, intramedullary metastases are rare with very few case reports in the literature available.

Methods

We present a case of a 3-year-old girl with a medulloblastoma who underwent surgical resection of spinal intramedullary metastases. Histopathology revealed the tumor to be an anaplastic medulloblastoma similar to the intracranial lesions. The patient subsequently underwent postoperative chemotherapy followed by radiotherapy.

Results

Following the surgery and subsequent follow-up, the patient showed a good recovery without any new neurological dysfunction.

Conclusions

Intramedullary metastasis of medulloblastoma remains a rare disease. Surgical resection could play a possible role in the management in addition to radiation and chemotherapy.

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Acknowledgements

We are grateful to the research grant from the Beijing Municipal Science & Technology Commission, PR China, No. Z171100001017140 (to AJS) and the Science Foundation of Military Medical Research and Clinical Research Foundation of PLA General Hospital in China, No. 2017FC-TSYS-2026.

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Correspondence to Aijia Shang.

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The authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or equity interest; and expert testimony or patent-licensing arrangements), or non-financial interest (such as personal or professional relationships, affiliations, knowledge, or beliefs) in the subject matter or materials discussed in this manuscript.

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Jiang, H., Luo, T., Tao, B. et al. Intramedullary metastasis in medulloblastoma: a case report and literature review. Childs Nerv Syst 37, 2091–2095 (2021). https://doi.org/10.1007/s00381-021-05086-y

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  • DOI: https://doi.org/10.1007/s00381-021-05086-y

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