Autor: |
Xinke Xu, MD, Junliang Li, MD, PhD, Yaqi Zheng, Fangcheng Li, MD, PhD |
Jazyk: |
angličtina |
Rok vydání: |
2019 |
Předmět: |
|
Zdroj: |
Interdisciplinary Neurosurgery, Vol 18, Iss , Pp - (2019) |
Druh dokumentu: |
article |
ISSN: |
2214-7519 |
DOI: |
10.1016/j.inat.2019.100480 |
Popis: |
Atypical teratoid/rhabdoid tumor (AT/RT) is a rare embryonal tumor of the central nervous system (CNS), which accounts for approximately 1–2% of all CNS neoplasms. Spinal canal is extremely rare. To our knowledge, there are only 16 cases of spinal AT/RT in children reported in English literature so far. Here we first presented a rare primary spinal AT/RT in a child with multiple vertebral subarachnoid metastasis. She was accepted surgical treatment and the diagnosis was established pathologically. She died 3 months later with no further therapy. We discuss the clinical presentation, imaging, pathology, treatment and prognosis of spinal AT/RT in children with the literature review. Keywords: Atypical teratoid/rhabdoid tumor, Spinal canal, Child |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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