RARE-32. PEDIATRIC METASTATIC SKULL BASE CHORDOMA WITH TP53 MUTATION – A CASE REPORT AND REVIEW OF THE LITERATURE

Chordoma is an uncommon bone tumor arising from notochordal remnant, which accounts for 1–4% of all bone malignancies. It commonly occurs along the cranial-spinal axis, and skull base is one of most frequent sites, representing 35–49% of all chordoma cases. Surgical resection is widely accepted as t...

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Bibliografiset tiedot
Julkaisussa:Neuro Oncol
Päätekijät: Shimada, Akira, Kurozumi, Kazuhiko, Kanamitsu, Kiichiro, Ishida, Hisashi Ishida, Fujiwara, Kaori, Washio, Kana Washio, Kumamoto, Tadashi, Ogawa, Chitose, Shin, Masahiro
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2020
Aiheet:
Craniopharyngioma and Rare Tumors
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7715982/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noaa222.742
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