Chordoid Meningioma: A Case Report.
10.3346/jkms.2003.18.5.768
- Author:
Je Young YEON
1
;
Jung Il LEE
;
Jong Hyun KIM
;
Yeon Lim SUH
Author Information
1. Department of Neurosurgery Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. jilee@smc.samsung.co.kr
- Publication Type:Case Report
- Keywords:
Meningioma;
Chordoma
- MeSH:
Adult;
Antigens, CD20/biosynthesis;
Antigens, CD3/biosynthesis;
B-Lymphocytes/pathology;
Brain/pathology;
Brain Neoplasms/*diagnosis/*pathology;
CA-15-3 Antigen/biosynthesis;
Chordoma/*diagnosis/*pathology;
Human;
Magnetic Resonance Imaging;
Male;
Meningeal Neoplasms/*diagnosis;
Meningioma/*diagnosis;
T-Lymphocytes/pathology;
Vimentin/biosynthesis;
Visual Fields
- From:Journal of Korean Medical Science
2003;18(5):768-771
- CountryRepublic of Korea
- Language:English
-
Abstract:
The term "chordoid meningioma" means meningioma, which is pathologically similar to chordoma, and previously reported that rarely associated with microcytic anemia and/or dysgammaglobulinemia especially in pediatric population. We present a case of this rare variant, which comprises less than 0.5% of all meningiomas. A 33-yr-old man visited our hospital, complaining visual field defect worsening over 7 yr. Neurological examination showed left homonymous hemianopsia. The brain magnetic resonance imaging revealed well enhancing right temporo-occipital mass with cystic portion. Histopathologic findings of resected tumor were compatible with chordoid meningioma which included trabeculae of eosinophilic, vacuolated cells in a myxoid matrix with prominent lymphoplasmacellular infiltration. The neoplastic cells were positive for vimentin and epithelial membrane antigen and negative for glial fibrillary acidic protein and cytokeratin. This is an adult case of chordoid meningioma without anemia or dysgammaglobulinemia.
