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ATRT of lateral ventricle in a child: A Rare Tumor at a Very Rare Location
Atypical teratoid/rhabdoid tumors (AT/RTs) of infancy are highly malignant central nervous system neoplasms that are most commonly seen during the first 2 years of life with limited therapeutic options. To date, only two cases have been described in the lateral ventricle. A 4-year-old boy presented...
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| Veröffentlicht in: | Asian J Neurosurg |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Wolters Kluwer - Medknow
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7057871/ https://ncbi.nlm.nih.gov/pubmed/32181209 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ajns.AJNS_128_19 |
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