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pubmed-article:9499227pubmed:abstractTextPilocytic Astrocytomas (WHO I) are histopathologically tumors of glial origin occurring predominantly in childhood and adolescence. Normally, they are characterized by a benign clinical course, with a long overall survival time and a high rate of complete remission. The rare case of pilocytic astrocytoma, primarily located in the third ventricular region, with generalized subarachnoidal spread is described. In the 10 years of follow-up, the histopathologic findings of the seedings remained those of a typical pilocytic astrocytoma; tumor progression did not occur.lld:pubmed
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pubmed-article:9499227pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:9499227pubmed:year1997lld:pubmed
pubmed-article:9499227pubmed:articleTitle[Pilocytic astrocytoma with subarachnoid dissemination].lld:pubmed
pubmed-article:9499227pubmed:affiliationAbteilung für Strahlentherapie der Radiologischen Universitätskliniken des Saarlandes, Homburg.lld:pubmed
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