ArticleWorld journal of clinical cases2019
Invasive myxopapillary ependymoma of the lumbar spine: A case report.
Article in World journal of clinical cases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 5 citations in OpenAlex.
- Epidemiological characteristics of myxopapillary ependymoma and factors affecting overall survival: a SEER-based analysis.Translational cancer research · 2024Article
- Myxopapillary Ependymoma Metastasis Mimicking Pulmonary Embolism: An Illustrative Case.Asian journal of neurosurgery · 2024Article
- Myxopapillary ependymoma with interval postoperative CSF seeding: A report of an unusual case.Radiology case reports · 2021Article
- Image report: Extensive disseminated thoracolumbosacral myxopapillary ependymoma.Surgical neurology international · 2020Article
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundMyxopapillary ependymomas are rare spinal tumours. Although histologically benign, they have a tendency for local recurrence. CASE SUMMARY: We describe a patient suffering from extra- and intradural myxopapillary ependymoma with perisacral spreading. He was treated with subtotal resection and postoperative radiation therapy. After treatment, he experienced slight sphincter disorders and lumboischialgic pain with no motor or sensory disturbances. Eight months later, a tumour regression was documented. The patient is still followed-up regularly.
conclusionLumbar myxopapillary ependymomas may present with lumbar or radicular pain, similar to more trivial lesions. Magnetic resonance imaging (MRI) is the primary modality for diagnosis. The treatment aim is to minimize both tumour and therapy-related morbidity and to involve different treatment modalities.
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