Meningioma and Cerebral Spindle Cell Sarcoma as Two Different Metachronous Tumor Entities Secondary to Medulloblastoma Treatment in Childhood: Case Report and Review of the Literature

Anna Jung; Michael Brodhun; Andreas Lemmer; Rüdiger Gerlach

doi:10.1055/a-2618-6807

Journal of Neurological Surgery Part A: Central European Neurosurgery, Table of Contents

J Neurol Surg A Cent Eur Neurosurg
DOI: 10.1055/a-2618-6807

Case Report

Meningioma and Cerebral Spindle Cell Sarcoma as Two Different Metachronous Tumor Entities Secondary to Medulloblastoma Treatment in Childhood: Case Report and Review of the Literature

Authors

Anna Jung

¹Department of Neurosurgery, HELIOS Klinikum Erfurt, Erfurt, Germany
Michael Brodhun

²Department of Pathology and Neuropathology, HELIOS Klinikum Erfurt, Erfurt, Germany
Andreas Lemmer

³Department of Pediatric Medicine 3, HELIOS Klinikum Erfurt, Erfurt, Germany
Rüdiger Gerlach

¹Department of Neurosurgery, HELIOS Klinikum Erfurt, Erfurt, Germany

Abstract

The authors report on a 21-year-old clinically asymptomatic female patient, who was admitted with two supratentorial intradural lesions in her follow-up magnetic resonance imaging 17 years after treatment of a posterior fossa medulloblastoma. Sequential surgical removal was performed. The left parietal tumor with dural involvement was diagnosed as a transitional meningioma WHO (World Health Organization) grade 1. The right temporal lesion, which had also close relationship to the dura, was diagnosed as a spindle cell sarcoma. We therefore report a metachronous tumor development of a benign and a malignant intradural sarcomatous tumor as secondary neoplasms following childhood medulloblastoma treatment.

Keywords

spindle cell sarcoma - meningioma - medulloblastoma

Full Text

References

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