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90, "link" : "/api/publicationsource/90", "label" : "SZTE Publicatio", "type" : { "otype" : "PublicationSourceType", "mtid" : 10007, "link" : "/api/publicationsourcetype/10007", "label" : "Repozitórium", "mayHaveOa" : true, "published" : true, "snippet" : true }, "name" : "SZTE Publicatio", "nameEng" : "SZTE Publicatio", "linkPattern" : "http://publicatio.bibl.u-szeged.hu/@@@", "publiclyVisible" : true, "published" : true, "oldId" : 90, "snippet" : true }, "oaType" : "CLOSED", "oaFree" : true, "validState" : "IDENTICAL", "idValue" : "12218", "realUrl" : "http://publicatio.bibl.u-szeged.hu/12218", "published" : false, "oldId" : 1660791, "snippet" : true } ], "journal" : { "otype" : "Journal", "mtid" : 2693, "link" : "/api/journal/2693", "label" : "JOURNAL OF NEURO-ONCOLOGY 0167-594X 1573-7373", "pIssn" : "0167-594X", "eIssn" : "1573-7373", "reviewType" : "REVIEWED", "noIF" : false, "sciIndexed" : true, "scopusIndexed" : true, "lang" : "FOREIGN", "hungarian" : false, "published" : true, 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It usually affects infants and young children under the age of 4 years and exhibits a very aggressive course with a dismal prognosis. For the 68 cases reported to date the mean age at diagnosis was 25.42 months (range 3-57 months). Survival data are available for 48 children (including our case): the median overall survival is 13.0 months, though 6 (9 %) of the children have had a relative long survival (>30 months). The aggressive combined treatment, involving primary surgical tumor removal, adjuvant polychemotherapy, including high-dose chemotherapy with stem cell transplantation, radiotherapy and radiochemotherapy, might play an important role in the longer survival. We have performed a literature review and we present here a multimodal-treated case of a 2- year-old girl with a long survival, who was reoperated when recurrence occurred. The residual tumor demonstrated a good response to temozolomide radiochemotherapy (craniospinal axis + boost) and followed by maintenance temozolomide. 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