Gewählte Publikation:
Dorfmüller, G; Würtz, FG; Umschaden, HW; Kleinert, R; Ambros, PF.
Intraspinal primitive neuroectodermal tumour: report of two cases and review of the literature.
Acta Neurochir (Wien). 1999; 141(11):1169-1175
Doi: 10.1007%2Fs007010050414
(- Case Report)
Web of Science
PubMed
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FullText_MUG
- Co-Autor*innen der Med Uni Graz
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Kleinert Reinhold
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- Abstract:
- Two patients with primary intraspinal primitive neuroectodermal tumour are presented. In a 32-year-old man, the tumour evolved intradurally from a sacral nerve root. Despite repeated surgery and radiochemotherapy, the patient suffered multiple intraspinal tumour relapses and intracranial seedings, and died 29 months after the first diagnosis. In a 17-year-old male adolescent, the tumour was located in the lumbar epidural space, extending into the paraspinal muscles. Following resection and radiochemotherapy, the patient is free from disease 23 months after the initial presentation. The clinical, radiological, histopathological and cytogenetic findings of both patients are presented and the relevant literature is reviewed. Particular attention is given to the histogenetic relationship between peripheral primitive neuroectodermal tumour and Ewing's sarcoma.
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Adolescent -
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Adult -
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Chemotherapy, Adjuvant -
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Combined Modality Therapy -
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Diagnostic Imaging -
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Disease Progression -
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Epidural Neoplasms - drug therapy
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Follow-Up Studies - drug therapy
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Humans - drug therapy
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Male - drug therapy
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Neuroectodermal Tumors, Primitive, Peripheral - drug therapy
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Peripheral Nervous System Neoplasms - drug therapy
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Radiotherapy, Adjuvant - drug therapy
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Spinal Neoplasms - drug therapy
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Spinal Nerve Roots - pathology
- Find related publications in this database (Keywords)
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Primitive Neuroectodermal Tumor
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Intraspinal Neoplasm
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Ewing Tumor