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Multifocal spinal malignant peripheral nerve sheath tumor in an immunocompromised individual: case report and review of literature

机译:免疫功能低下个体的多灶性脊柱恶性周围神经鞘瘤:病例报告和文献复习

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PurposePrimary intraosseous spinal malignant peripheral nerve sheath tumor (MPNST) is exceedingly rare. MPNST with multifocal origin has been described to occur in the extremities. Such a lesion has not been described to occur in the spine. We describe a case of multifocal spinal MPNST and to review the literature relevant to this rare entity and its management.MethodsA 40-year-old immunodeficient patient presented with rapidly progressive paraparesis and mid back ache.ResultsDespite aggressive surgical decompression, he developed multiple metastases 3?months after surgery. However, he remained stable for 1?year without any adjuvant therapy. Presently, he has received palliative radiotherapy for spinal recurrence and cerebral metastasis.ConclusionMultifocal spinal MPNST is a rare lesion. In this instance, the multifocality of the disease and its odd location could be attributed to the immunodeficiency state. The prolonged survival could be due to an improvement in his immune status due to HAART...
机译:目的原发性骨内脊柱恶性周围神经鞘瘤(MPNST)极为罕见。具有多灶性起源的MPNST被描述为发生在四肢。尚未描述这种病变在脊柱中发生。我们描述了一例多发性脊柱MPNST病例,并复习了与该罕见病及其治疗相关的文献。方法一名40岁免疫缺陷患者表现为快速进行性轻瘫和中背部疼痛。术后几个月。然而,他在没有任何辅助治疗的情况下保持稳定1年。目前,他因脊柱复发和脑转移接受了姑息性放射治疗。结论多灶性脊柱MPNST是一种罕见的病变。在这种情况下,疾病的多灶性及其奇异位置可归因于免疫缺陷状态。延长的生存期可能是由于HAART改善了他的免疫状况。

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