Primary intracranial leiomyosarcoma: a case report and review of the literature

Introduction Malignant tumours of the central nervous system (CNS) represent the second most common cancer type in the paediatric population of developed countries, and mortality caused by CNS tumours is the highest among paediatric cancers. Tumours of mesenchymal origin occurring either as primary...

Full description

Saved in:
Bibliographic Details
Published inChild's nervous system Vol. 25; no. 8; pp. 1013 - 1017
Main Authors Mathieson, C. S, St George, E. J, Stewart, W, Sastry, J, Jamal, S
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Berlin/Heidelberg : Springer-Verlag 01.08.2009
Springer-Verlag
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Introduction Malignant tumours of the central nervous system (CNS) represent the second most common cancer type in the paediatric population of developed countries, and mortality caused by CNS tumours is the highest among paediatric cancers. Tumours of mesenchymal origin occurring either as primary or secondary lesions of the central nervous system are very rare in children. This paper describes the case of a 5-year-old non-immunocompromised male who presented with a right frontal primary intracranial leiomyosarcoma associated with large subdural collections. Discussion and conclusion Following surgical excision and adjuvant chemoradiotherapy, the patient has remained disease-free for 18 months. The literature is reviewed and the possible association of the chronic subdurals to the later development of the leiomyosarcoma explored.
Bibliography:http://dx.doi.org/10.1007/s00381-009-0845-3
ObjectType-Case Study-3
SourceType-Scholarly Journals-1
content type line 23
ObjectType-Review-1
ObjectType-Feature-5
ObjectType-Report-2
ObjectType-Article-4
ObjectType-Article-2
ObjectType-Feature-1
ISSN:0256-7040
1433-0350
DOI:10.1007/s00381-009-0845-3