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• W166348567 startingPage "187" @default.
• W166348567 abstract "Intramedullary spinal cord tumors (IMSCT) are rare and account for only 5–6% of all central nervous systems (CNS) tumors (Sloof and McCarthy 1964; Goh et al. 1997b; Houten and Weiner 2000). These tumors can occur at any age, but most are identified during the first three decades of life. Approximately 100–200 cases of pediatric IMSCT are diagnosed each year in the United States (Constantini and Epstein 1996). Primary glial tumors such as ependymomas, astro-cytomas, and gangliogliomas account for at least 80% of IMSCTs (Cooper 1989; McCormick et al. 1990b; Sandler et al. 1992; Epstein et al. 1993; Cristante and Herrmann 1994; Hoshimaru et al. 1999), and nearly 60% occur in the cervical and cervicothoracic region (Cooper 1989). The presenting symptoms are usually minimal, and parents typically report symptoms for months or years prior to diagnosis (Kothbauer 2007). The common clinical features are pain, weakness, par-esthesias, spinal deformity, sphincter disturbance, and cervicomedullary symptoms (Goh et al. 1997). Slow progressive deterioration of neurologic function can also occur (Constantini and Epstein 1996; Kothbauer 2007). The surgical objective for primary IMSCTs is gross total resection, but in some cases, achieving this goal may leave a patient with severe neurologic deficits. The location of the tumor, age of the patient, pathology, and ability to achieve a gross total resection usually determine whether radiation or chemotherapy will be used." @default.
• W166348567 created "2016-06-24" @default.
• W166348567 creator A5054902298 @default.
• W166348567 creator A5090727974 @default.
• W166348567 date "2010-01-01" @default.
• W166348567 modified "2023-09-26" @default.
• W166348567 title "Intramedullary Spinal Cord Tumors" @default.
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