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Case report: Halo-pelvic traction linked to diplopia and tongue deviation in adolescent scoliosisCan a rare spine treatment cause vision and tongue problems in a child?

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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.

Imagine a child undergoing a major procedure to straighten a severely curved spine, only to face a new and frightening problem: seeing double and losing control of her tongue. That's what happened to a 12-year-old girl after about 40 days of a treatment called halo-pelvic traction, which uses an external frame to slowly lengthen the spine.

Her symptoms—painless double vision and her tongue deviating to the left—appeared after her spine had been lengthened by roughly 12 centimeters. The medical team stopped the traction treatment and started a therapy aimed at supporting nerve health. Over the next 50 days, her symptoms gradually faded away.

This is a detailed report of just one patient's experience. Because it's a single case, we can't say for certain that the traction treatment caused the nerve issues, only that the problems appeared during the treatment. It also doesn't tell us how often this might happen to other children. The report suggests that stopping the treatment quickly when such symptoms appear might help prevent lasting nerve damage, but more evidence is needed to be sure.

What this means for you:
A single case links a spine-stretching treatment to temporary nerve problems in a child.

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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