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SHR Neuro Krebs Kardio Lipid Stoffw Microb

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
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Führende Autor*innen der Med Uni Graz
Benesch Martin
Co-Autor*innen der Med Uni Graz
Eder Hans
Lackner Herwig
Nebl Andrea Maria
Ritter-Sovinz Petra
Schwinger Wolfgang
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)
Antineoplastic Combined Chemotherapy Protocols -
Child, Preschool -
Combined Modality Therapy -
Cranial Irradiation -
Down Syndrome - complications
Humans -
Magnetic Resonance Imaging -
Male -
Medulloblastoma - diagnosis
Remission Induction -

Find related publications in this database (Keywords)
Down syndrome
medulloblastoma
metastases
multimodality treatment
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