Journal of Pediatric Neuroradiology 2012; 01(04): 283-286
DOI: 10.3233/PNR-2012-035
Georg Thieme Verlag KG Stuttgart – New York

Intracranial primitive neuroectodermal tumor in a child previously treated for Ewing sarcoma

Ihsan Anık
a   Department of Neurosurgery, School of Medicine, Kocaeli University, Kocaeli, Turkey
,
Mehmet Korkmaz
a   Department of Neurosurgery, School of Medicine, Kocaeli University, Kocaeli, Turkey
,
Yonca Anık
b   Department of Radiology, School of Medicine, Kocaeli University, Kocaeli, Turkey
,
Kenan Koç
a   Department of Neurosurgery, School of Medicine, Kocaeli University, Kocaeli, Turkey
,
Demir Kürşat Yıldız
c   Department of Pathology, School of Medicine, Kocaeli University, Kocaeli, Turkey
,
Funda Çorapcıoğlu
d   Department of Pediatrics, School of Medicine, Kocaeli University, Kocaeli, Turkey
,
Savaş Ceylan
a   Department of Neurosurgery, School of Medicine, Kocaeli University, Kocaeli, Turkey
,
Safiye Sanem Bulut
b   Department of Radiology, School of Medicine, Kocaeli University, Kocaeli, Turkey
› Author Affiliations

Subject Editor:
Further Information

Publication History

24 January 2011

23 March 2011

Publication Date:
28 July 2015 (online)

Abstract

A case of surgically resected solitary parenchymal brain tumor in a 13-year-old girl, who was treated 18 months ago with chemotherapy and radiotherapy for cervical vertebral Ewing sarcoma is presented. The intracranial primitive neuroectodermal tumor was detected after admission for severe headache. No other metastasis or recurrences were encountered following 14 months after brain surgery. The authors discuss whether this parenchymal brain tumor was a metastasis or a second primary Ewing sarcoma/primitive neuroectodermal tumor.