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Benesch, M; Moser, A; Sovinz, P; Lackner, H; Schwinger, W; Eder, H; Urban, C.
Medulloblastoma in a child with down syndrome: long-term remission with multimodality treatment.
Pediatr Blood Cancer. 2009; 53(6): 1150-1151.
Doi: 10.1002/pbc.22109
Web of Science
PubMed
FullText
FullText_MUG
- Führende Autor*innen der Med Uni Graz
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Benesch Martin
- Co-Autor*innen der Med Uni Graz
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Eder Hans
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Lackner Herwig
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Nebl Andrea Maria
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Ritter-Sovinz Petra
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Schwinger Wolfgang
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Urban Ernst-Christian
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- Abstract:
- A 4(3/4)-year-old male with Down syndrome (DS) presented with unsteady gait and fatigue. Neuroimaging revealed a cerebellar mass with concomitant obstructive hydrocephalus and additional metastatic lesions. He was successfully treated and is still in complete remission 5 years from diagnosis. The present case illustrates that, although not yet reported, medulloblastoma can also occur in patients with DS.
- Find related publications in this database (using NLM MeSH Indexing)
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Antineoplastic Combined Chemotherapy Protocols -
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Child, Preschool -
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Combined Modality Therapy -
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Cranial Irradiation -
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Down Syndrome - complications
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Humans -
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Magnetic Resonance Imaging -
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Male -
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Medulloblastoma - diagnosis
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Remission Induction -
- Find related publications in this database (Keywords)
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Down syndrome
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medulloblastoma
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metastases
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multimodality treatment