Bartman Mason, D'Souza Preston, Malkova Kseniia, Peterson Joshua Michael, Currie Joshua, Costa Matias, Felicella Michelle Madden, Lall Rishi
John Sealy School of Medicine, The University of Texas Medical Branch, Galveston, Texas.
Department of Neurosurgery, The University of Texas Medical Branch, Galveston, Texas.
J Neurosurg Case Lessons. 2025 Mar 24;9(12). doi: 10.3171/CASE24723.
Malignant peripheral nerve sheath tumors (MPNSTs) are rare and highly malignant tumors of neural crest origin. No matter their anatomical location, they are difficult to treat and carry a poor prognosis.
This report highlights the complexities of the diagnosis and management of a patient with MPNST of the cauda equina. The tumor retained the expression of H3K27me3, which is expected in spinal MPNSTs but uncommon in most sporadic and neurofibromatosis type 1-driven MPNSTs.
The described diagnostic nuance should be taken into consideration in patients with suspected MPNST of the cauda equina, as these tumors require swift neurosurgical intervention in order to maintain neurological function. Additional treatment modalities include neoadjuvant and adjuvant chemotherapy and radiotherapy. Although improvements in local control and progression-free survival have been reported, the role of radiation therapy and chemotherapy has been underinvestigated due to the rarity of MPNSTs presenting in this region. https://thejns.org/doi/10.3171/CASE24723.
恶性外周神经鞘瘤(MPNSTs)是起源于神经嵴的罕见且高度恶性的肿瘤。无论其解剖位置如何,都难以治疗且预后较差。
本报告强调了一名马尾神经MPNST患者诊断和管理的复杂性。该肿瘤保留了H3K27me3的表达,这在脊髓MPNST中是预期的,但在大多数散发性和1型神经纤维瘤病驱动的MPNST中并不常见。
对于疑似马尾神经MPNST的患者,应考虑到所描述的诊断细微差别,因为这些肿瘤需要迅速的神经外科干预以维持神经功能。其他治疗方式包括新辅助化疗和辅助化疗以及放疗。尽管有报道称局部控制和无进展生存期有所改善,但由于该区域出现的MPNST罕见,放疗和化疗的作用尚未得到充分研究。https://thejns.org/doi/10.3171/CASE24723