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Spinal schwannomas represent benign neoplasms arising from spinal nerve root sheaths, predominantly occurring in the cauda equina region. By reviewing this case and literature, our aim was to highlight the diagnostic and therapeutic considerations in managing such rare and challenging cases in the pediatric population. We present an exceptional pediatric case of a giant thoracolumbosacral schwannoma with multi-root involvement, neuroimaging revealed a 36-cm intradural mass extending from T10 to the coccyx, representing the longest documented spinal schwannoma to date. Taking into account the patient’s previous cervical spinal canal meningioma surgical history, the coexistence of a schwannoma added complexity to the preoperative diagnosis. Under intraoperative neurophysiological monitoring (IONM), multi-level laminectomy with anatomical reconstruction and tumor resection from T10 to S4 was performed. The pathological result confirmed it to be a schwannoma. The coexistence of two types tumors within the spinal canal is rare, in addition to MRI scans, pathological diagnosis is gold standard at this time, and surgery is still the preferred option.
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http://dx.doi.org/10.1007/s12672-025-03469-0 | DOI Listing |
Discov Oncol
August 2025
Department of Neurosurgery, The First Hospital of Hebei Medical University, Shijiazhuang, 050000, China.
Spinal schwannomas represent benign neoplasms arising from spinal nerve root sheaths, predominantly occurring in the cauda equina region. By reviewing this case and literature, our aim was to highlight the diagnostic and therapeutic considerations in managing such rare and challenging cases in the pediatric population. We present an exceptional pediatric case of a giant thoracolumbosacral schwannoma with multi-root involvement, neuroimaging revealed a 36-cm intradural mass extending from T10 to the coccyx, representing the longest documented spinal schwannoma to date.
View Article and Find Full Text PDFOper Neurosurg
September 2021
Division of Pediatric Neurosurgery, Department of Surgery, Texas Children's Hospital, Houston, Texas, USA.
Extensive multifocal intradural lesions in children present a formidable challenge. This surgical video illustrates our management of a 14-yr=old boy with two intradural mass lesions on magnetic resonance imaging (MRI): one at T2-5 and the other from T12 through the sacral cul-de-sac. In a single procedure, we performed a T2-5 laminectomy and laminoplasty and T12-sacrum laminectomy for tumor resection.
View Article and Find Full Text PDFAsian J Neurosurg
February 2015
Department of Neurosurgery, Padmashree Dr. D. Y. Patil Hospital, Pimpri, Pune, Maharashtra, India.
We report two cases with giant intramedullary epidermoid cysts in the thoracolumbosacral and lumbosacral regions with varied presentations. Magnetic resonance (MR) imaging of the thoraco lumbar spine in case 1revealed an intramedullary elongated mass extending from T10 to S2 level causing significant widening of the spinal canal while MR imaging of lumbosacral spine in case 2 showed straightening of the lumbar spine and spina bifida at L5 level with conus at L3 and a lobulated long segment intramedullary solid cystic lesion extending from L2 to S2 veterbrae. The lesion was surgically resected and the pathology revealed an epidermoid cyst.
View Article and Find Full Text PDFZhonghua Zhong Liu Za Zhi
March 2013
Department of Orthopaedics, Qilu Hospital of Shandong University, Jinan 250012, China.
Objective: To investigate the therapeutic effect of total en bloc spondylectomy (TES) for thoracolumbar tumors and the results of spinal stability reconstruction.
Methods: From January 2007 to June 2011 there were 18 patients with thoracolumbar tumors distributed in the thoracic vertebrae (n = 10) and lumbar vertebrae (n = 8). There were 7 haemangiomas, 5 giant cell tumors of bone, 1 malignant schwannoma, 1 solitary plasmocytoma, 1 neuroblastoma, 1 osteoblastoma, 1 metastatic malignant fibrous histiocytoma, and 1 metastasis of breast cancer.
Pediatr Surg Int
March 1996
Department of Neurosurgery, Assaf Harofeh Medical Center, 70300, Zerifin, Israel.
A case of sacrococcygeal teratoma with unusually high intraspinal extension is reported and the symptomatology and treatment are discussed. A 7-month-old male presented at birth with a prominent mass of the right gluteal region preventing him from straightening his legs and causing undue effort during defecation. Magnetic resonance T1-weighted imaging revealed a thoracolumbosacrococcygeal, partly cystic tumor with intraspinal extension up to the mid-thoracic spine.
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