| Literature DB >> 16126883 |
A J Clarke1, T S Jacques, M J Galloway, M Thom, N D Kitchen, G T Plant.
Abstract
Inflammatory myofibroblastic tumours (IMTs) are an uncommon spindle cell neoplasm with a dense inflammatory infiltrate, usually encountered in children. IMTs of the central nervous system are extremely rare. This report describes the case of an IMT in a 61 year old man, in the pineal region. The tumour was completely excised, and immunohistochemistry demonstrated anaplastic lymphoma kinase 1 expression. There was no tumour recurrence during 18 months of follow-up. Our case extends both the age range and sites of occurrence of this rare tumour.Entities:
Mesh:
Substances:
Year: 2005 PMID: 16126883 PMCID: PMC1770811 DOI: 10.1136/jcp.2004.022947
Source DB: PubMed Journal: J Clin Pathol ISSN: 0021-9746 Impact factor: 3.411