Pavlina Lenga (Heidelberg), Daniel Kühlwein (Heidelberg), Martin Grutza (Heidelberg), Mohammed Issa (Heidelberg), Felix Hinz (Heidelberg), Felix Sahm (Heidelberg), Florian Selt (Heidelberg), Till Milde (Heidelberg), Patrick Günther (Heidelberg), Andreas Unterberg (Heidelberg), Sandro Krieg (Heidelberg), Ahmed El Damaty (Heidelberg)
Spinal cord compression caused by tumor related process (SCC) often results in dire prognosis, carrying risks such as permanent paralysis, sensory loss, and sphincter dysfunction. Data on the incidence and etiology of SCC caused by tumorous process in pediatric populations are markedly scant. Our study investigates the etiology, clinical manifestation, treatment, and outcomes of pediatric SCC patients inflicted by various tumor types and provides a comprehensive review of the existing literature on this subject.
We conducted a retrospective review of our institutional pediatric oncology and neurosurgery database, examining 14 patients under 18 years admitted with SCC due to oncological diseases since 2005. We analyzed the clinical presentations, evaluations, molecular diagnostics and treatments for these patients.
14 pediatric patients, each diagnosed with distinct spinal tumor entity were included. The mean patient age was approximately 19.6 ± 10.1 months. Severe spinal cord pain was observed in 13 patients, while acute neurological deterioration manifested in 7 patients. As a first-line intervention, 13 patients underwent decompressive surgery through laminectomy and tumor resection, and only one patient received chemotherapy solely. Before surgery, seven patients were unable to walk; post-surgery, six of them regained their ability to ambulate. The diagnosis encompassed a range of neoplasms: two instances of Ewing sarcoma, 3 instances of teratoma, one case presenting an atypical teratoid Rhabdoid tumor, two instances each of low-grade astrocytoma and neuroblastoma, and single instances of ependymoma, meningioma, rhabdomyosarcoma, and embryonal tumors with multilayered rosettes (ETMRs). Three patients succumbed two years after initiating therapy.
Despite their rarity, intraspinal tumors in pediatric patients pose substantial therapeutic challenges. The intertwined complexities of the disease entity and the patient's neurological status demand swift initiation of an individualized therapeutic strategy. This crucial step helps optimize outcomes for this patient cohort, who frequently grapple with debilitating health conditions. Inclusion of these patients within a registry is mandatory to optimize treatment outcomes due to their rarity in pediatric population.
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