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.
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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
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