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Gewählte Publikation:

Dorfmüller, G; Würtz, FG; Kleinert, R; Lanner, G.
Cerebral primitive neuro-ectodermal tumour following treatment of a unilateral retinoblastoma.
Acta Neurochir (Wien). 1997; 139(8):749-755 Doi: 10.1007/BF01420048 (- Case Report)
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Co-Autor*innen der Med Uni Graz
Kleinert Reinhold
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Abstract:
Cerebral primitive neuro-ectodermal tumour (PNET) occurring as a second primary malignancy in childhood is exceedingly rare. We present a 7-year-old boy who developed a proven supratentorial PNET five years after enucleation and radio-/chemotherapy for a sporadic, unilateral retinoblastoma with optic nerve invasion. The association with this malignant eye disease as well as the effect of irradiation and multi-agent chemotherapy on second tumour induction are evaluated.
Find related publications in this database (using NLM MeSH Indexing)
Chemotherapy, Adjuvant -
Child -
Combined Modality Therapy -
Eye Enucleation -
Humans -
Magnetic Resonance Imaging -
Male -
Neoplasm Invasiveness -
Neoplasms, Second Primary - diagnosis
Neuroectodermal Tumors, Primitive - diagnosis
Optic Nerve - pathology
Postoperative Complications - diagnosis
Radiotherapy, Adjuvant - diagnosis
Retinal Neoplasms - genetics
Retinoblastoma - genetics
Risk Factors - genetics
Supratentorial Neoplasms - diagnosis

Find related publications in this database (Keywords)
Retinoblastoma
Primitive Neuro-Ectodermal Tumor
Radio-/Chemotherapy
2nd Primary Malignancy
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