Severe scoliosis associated with Costello syndrome: a case report.

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Abstract

Costello syndrome is characterised by dwarfism, unique cutaneous lesions, a distinct facial gestalt, and mental retardation. There have been no detailed reports of severe spinal deformities requiring surgical treatment as a complication of Costello syndrome. We report a case of a 10-year-old girl with progressive scoliosis associated with Costello syndrome. She underwent anterior release and posterior surgical correction and fusion from T5 to L2 using a third generation hook and rod system plus spinous process wiring. Congenital portal vein deficiency and coagulopathy were other major complications. At 15-month follow-up, the patient had good balance and no evidence of instrumentation failure.

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Motosuneya, T., Asazuma, T., Tsuji, T., Watanabe, H., Nakayama, Y., & Nemoto, K. (2006). Severe scoliosis associated with Costello syndrome: a case report. Journal of Orthopaedic Surgery (Hong Kong), 14(3), 346–349. https://doi.org/10.1177/230949900601400324

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