| Literature DB >> 11155064 |
Y Tohma1, T Kaneko, D Kita, M Iwato, Y Hayashi, O Tachibana, M Hasegawa, J Yamashita.
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. Copyright 2001 S. Karger AG, Basel.Entities:
Mesh:
Year: 2000 PMID: 11155064 DOI: 10.1159/000055966
Source DB: PubMed Journal: Pediatr Neurosurg ISSN: 1016-2291 Impact factor: 1.162