Cervical Meningeal Chondroma: A Case ReportSoichiro Takamiya1*, Toshitaka Seki1, Kikutaro Tokairin1, Syuji Hamauchi1, Toru Sasamori1, Tomoko Mitsuhashi2, Kiyohiro Houkin1
- *Corresponding Author:
- Soichiro Takamiya, M.D.
Department of Neurosurgery
Hokkaido University Graduate School of Medicine
N-15, W-7, Kita-ku, Sapporo, Hokkaido 060-8638, Japan
E-mail: [email protected]
Received date: September 24, 2016; Accepted date: October 13, 2016; Published date: October 15, 2016
Citation: Takamiya S, Seki T, Tokairin K, Hamauchi S, Sasamori T, et al. (2016) Cervical Meningeal Chondroma: A Case Report. J Spine 5:335. doi: 10.4172/2165-7939.1000335
Copyright: © 2016 Takamiya S. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Spinal chondromas are rare tumors, usually classified as periosteal chondroma or enchondroma, according to their origin. We describe a rare case of cervical spine meningeal chondroma in a 79-year-old man, who presented with right-sided weakness and lower-extremity dysesthesia. Magnetic resonance imaging revealed a tumor at the C1-C2 level. We suspected it to be meningioma and performed tumor excision. However, the final pathology diagnosed it as a meningeal chondroma. After surgery, his symptoms gradually improved. This case shows that, although uncommon, spinal chondromas may arise from the meninges. A good outcome is expected after total resection of the tumor.