Abstract
The authors report an extremely rare case of de novo spinal teratoma after treatment for intracranial germ cell tumor. A 17-year-old male developed pain of bilateral lower extremities and urinary retention 18 months after complete remission of intracranial mixed germ cell tumor. Magnetic resonance imaging revealed a huge spinal tumor associated with spina bifida occulta. Total resection was performed, and histogenetical findings led to the diagnosis of a mature teratoma with normal p16 gene, whereas analysis of intracranial tumor showed p16 deletion. The spinal anomaly and genetic analysis strongly suggest that the spinal teratoma was a de novo tumor rather than a metastasis or dissemination of the original intracranial germ cell tumor.
Original language | English |
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Pages (from-to) | 261-264 |
Number of pages | 4 |
Journal | Pediatric Neurosurgery |
Volume | 33 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2000 |
All Science Journal Classification (ASJC) codes
- Pediatrics, Perinatology, and Child Health
- Surgery
- Clinical Neurology