A 13-year patient journey of infant giant clival chordoma: case report and literature review

1Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Chordomas are rare malignant bone tumours that develop from the ectopic remnants of the embryonic notochord. In contrast to adults, the majority in children under 16 present intra-cranially (63%). In 2006, we reported the youngest case of a large clival chordoma, a 15-week old baby, the second case to present without skull base involvement and the fourth case of chordoma in a patient with tuberous sclerosis (TS) Kombogiorgas (Childs Nerv Syst 22(10):1369–1374, 2006). In this report, we provide an update on this patient’s journey through a range of therapeutic options and summarize an update of the literature, since 2006, for this patient group.

Author supplied keywords

Cite

CITATION STYLE

APA

Apps, J., Gagen, R., Neumann, E., Solanki, G., & English, M. (2023). A 13-year patient journey of infant giant clival chordoma: case report and literature review. Child’s Nervous System, 39(4), 1077–1081. https://doi.org/10.1007/s00381-022-05749-4

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free