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Case report: Halo-pelvic traction linked to diplopia and tongue deviation in adolescent scoliosis

Case report: Halo-pelvic traction linked to diplopia and tongue deviation in adolescent scoliosis
Photo by Cht Gsml / Unsplash
Key Takeaway
Consider monitoring for cranial nerve symptoms in patients undergoing halo-pelvic traction, based on a single case report.

A case report describes a 12-year-old female with severe congenital scoliosis who underwent halo-pelvic traction. After 40 days of traction, with approximately 12 cm of total longitudinal lengthening, the patient developed painless horizontal diplopia, leftward deviation of the protruded tongue, and limited abduction of the left eye.

The traction was discontinued, and neurotrophic therapy was initiated. The symptoms gradually resolved within 50 days after stopping traction. The report notes 1 patient experienced these adverse events and 1 patient had resolution of symptoms. No serious adverse events, discontinuation rates beyond the case, or tolerability data were reported.

This is a single case report with no control group, comparator, or statistical analysis. The publication type is a case report, and key details like study phase, setting, primary outcome, follow-up duration, and funding/conflicts were not reported. The authors describe only a temporal association; no causal inference can be made from this evidence.

The practice relevance suggested by the report is that early recognition and discontinuation of traction, combined with multimodal therapy, may help prevent permanent cranial nerve injury. However, given the limitations, this represents a hypothesis for further study rather than established clinical guidance. Clinicians should be aware of this potential neurological complication but cannot generalize from one case.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedMar 2026
View Original Abstract ↓
ObjectiveTo report a case of diplopia and tongue deviation following halo-pelvic traction (HPT) in a patient with severe congenital scoliosis (CS) and to analyze the potential causes.MethodsA retrospective analysis of the patient's clinical data was conducted, including medical history, physical examination, imaging findings, treatment course, and outcomes.ResultsA 12-year-old female with CS was admitted. After 40 days of traction (with a total longitudinal lengthening of approximately 12 cm), she developed painless horizontal diplopia and leftward deviation of the protruded tongue. Physical examination revealed limited abduction of the left eye and leftward deviation of the protruded tongue. Traction was discontinued, and neurotrophic therapy (including corticosteroids, mecobalamin, and B-complex vitamins) was initiated. Symptoms gradually resolved within 50 days, with complete resolution of diplopia and normalized tongue protrusion.ConclusionEarly recognition and discontinuation of traction, combined with multimodal therapy, may prevent permanent cranial nerve injury in patients undergoing HPT.
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