Cent Eur Neurosurg 2008; 69(4): 194-199
DOI: 10.1055/s-2008-1077079
Case Report

© Georg Thieme Verlag KG Stuttgart · New York

Meningioma 40 Years after Radiation Therapy for Retinoblastoma: Genetic and Phenotypic Analysis, and Minireview of Literature

Meningeom 40 Jahre nach Strahlentherapie für Retinoblastom: genetische und phenotypische Analyse und kleine Zusammenfassung der LiteraturV. Balik 1 , M. Sarissky 2 , D. Lohmann 3 , I. Sulla 4
  • 1Department of Neurosurgery, Faculty of Medicine, P. J. Safarik University, Kosice, Slovakia
  • 2Department of Pharmacology, Faculty of Medicine, P. J. Safarik University, Kosice, Slovakia
  • 3Klinische Forschergruppe Ophthalmologische Onkologie und Genetik, Universitätsklinikum Essen, Institut für Humangenetik, Essen, Germany
  • 4Department of Neurosurgery, Faculty of Medicine, AD Centre, Pavol Jozef Safarik University in Kosice, Kosice, Slovakia
Further Information

Publication History

Publication Date:
29 July 2008 (online)

Abstract

The authors present a case of 44-year-old Caucasian female diagnosed with meningothelial meningioma 40 years after radiotherapy for sporadic unilateral retinoblastoma. The genetic analysis of DNA from the meningioma revealed no oncogenic mutation in the RB1 gene. The analysis of meningioma cells by flow cytometry revealed the following immunophenotype: vimentin++ CD56+ GFAP− EGFR−. Intermediate intensities of Her-2/neu and Pgp expression were detected in a small percentage of tumour cells. Data suggest that the tumour was most likely induced by radiotherapy and did not arise as a second tumour as there was no hereditary predisposition to retinoblastoma.

Zusammenfassung

Die Autoren präsentieren den Fall einer 44-Jahre alten Kaukasierin, bei der ein meningotheliales Meningeom 40 Jahre nach Radiotherapie eines unilateralen Retinoblastoms diagnostiziert wurde. Die genetische Analyse der DNA des Meningeoms zeigte keine onkogenetischen Mutationen im RB1 Gen. Die Analyse der Meningeomzellen durch die Flow Cytometrie zeigte folgenden Immunphenotyp: vimentin++ CD56+ GFAP EGFR. Die durchschnittlichen Intensitäten von Her-2/neu und Pgp Expressionen wurden in kleinen Proportionen in einigen Tumorzellen gefunden. Diese Daten belegen, dass der Tumor höchstwahrscheinlich durch die Radiotherapie induziert wurde und nicht als Sekundärtumor bei hereditärer Prädisposition zu einem Retinoblastom zu sehen ist.

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Correspondence

Prof. I. Sulla

Department of Neurosurgery

Faculty of Medicine

AD Centre

Pavol Jozef Safarik University in Kosice

Trieda SNP 1

04011 Kosice

Slovakia

Phone: +421/55/640 25 74

Fax: +421/55/642 81 51

Email: isulla@upjs.sk

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