Introduction The majority of chordomas occur between the fifth and seventh decades of life and are thus extremely rare in children, which account for less than 5% of all spinal chordoma cases. Case report We report on the development of this rare condition in two boys aged 7 and 10 years. One patient presented with a palpable neck mass and dysphagia, while the other presented with posterior neck pain. Radiological studies revealed an extensive mass in the cervical vertebrae and paravertebral soft tissue of both patients. The tumors were subtotally removed in an attempt to improve the success of adjuvant proton beam radiotherapy. Pathological examination, which included immunohistochemical staining, revealed chordoma of the cervical spine in both patients. Conclusion Although en bloc resection is the ideal modality for treatment of chordoma, such a procedure is often associated with a significant risk of surgical morbidity due to the tumor location. Therefore, piecemeal resection followed by postoperative adju ant radiotherapy, including proton radiotherapy or radiosurgery, should be considered in such cases.
|Number of pages||6|
|Journal||Child's Nervous System|
|Publication status||Published - 2010 Jun|
Bibliographical noteFunding Information:
Acknowledgements This study was supported by a Korea Research Foundation grant (KRF-2008-313-H00022) funded by the Korean government and a grant from the Stem Cell Research Center (SC-4180) of the 21st Century Frontier Research Program funded by the Ministry of Education, Science and Technology, Republic of Korea.
All Science Journal Classification (ASJC) codes
- Pediatrics, Perinatology, and Child Health
- Clinical Neurology