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- W162882786 abstract "Pediatric Atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous system (CNS) are among the most malignant neoplasms and most often diagnosed in children smaller than 3 years of age and incidence is 1–2% of all brain tumors in children. Sixty-three percent of the AT/RT of the CNS is seen in infra-tentorial compartment, there are no precise imaging features that differentiate AT/RT from the other posterior fossa tumor. The “rhabdoid” cells are characteristic on cytopathology. It has been established now that CNS, AT/RT often shows deletion of the long arm of chromosome 22q11.2. The initial treatment for most children with AT/RT is surgical with and without cerebrospinal fluid diversionary procedure. Children with less than 3 years of age offered chemotherapy but in older children radiotherapy is given in addition." @default.
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- W162882786 date "2012-01-01" @default.
- W162882786 modified "2023-09-27" @default.
- W162882786 title "Pediatric Atypical Teratoid/Rhabdoid Tumors (An Overview)" @default.
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- W162882786 doi "https://doi.org/10.1007/978-94-007-2957-5_1" @default.
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