| Literature DB >> 27465420 |
Yoen-Young Chuah1, Tsewang Tashi2, Cherng-Gueih Shy3, Jean-Shiunn Shyu4, Ming-Jeng Dong5, Er-Jung Hsueh6.
Abstract
CASE DESCRIPTION: A 20-year-old woman presented with a rare intracranial inflammatory myofibroblastic tumor (IMT) manifesting as headache and insomnia. Magnetic resonance imaging showed a tumorous lesion with heterogeneous enhancement at the right temporal lobe, as well as perifocal edema with midline shift. The tumor was totally resected with the margin free. Pathologic examination showed IMT with myofibroblastic cells admixed with collagen fibers. Sarcomatous change in morphology was observed in tumor recurrence within 7 months.Entities:
Keywords: Anaplastic lymphoma kinase; Brain; Inflammatory myofibroblastic tumor; Recurrence; Sarcomatous change
Mesh:
Year: 2016 PMID: 27465420 DOI: 10.1016/j.wneu.2016.07.060
Source DB: PubMed Journal: World Neurosurg ISSN: 1878-8750 Impact factor: 2.104