Case reportEffective cauda equina decompression in two siblings with Charcot-Marie-Tooth disease type 1B

- Two siblings with Charcot-Marie-Tooth (CMT) 1B and a cauda syndrome are presented.
- The cauda syndrome was in both patients caused by hypertrophic nerve roots totally filling the spinal canal.
- Acute decompression of the caudal nerve roots was shown to be a safe and effective treatment, also on the long term.

Two siblings with Charcot-Marie-Tooth (CMT) 1B due to a c.517G>C (p.Gly173Arg) mutation in the MPZ gene both developed an acute cauda syndrome with unbearable back pain radiating to both legs, progressive muscle weakness of the legs, and saddle hypesthesia with fecal and urinary incontinence. MRI showed in both patients a lumbar spinal canal totally filled with hypertrophic caudal nerve roots. We performed acute decompression. Postoperatively, in both patients, the back pain resolved immediately, there was a significant improvement of both the paresis of the legs and the hypesthesia, and there was a full return of continence. There was no recurrence of acute symptoms during respectively 19 years and 1.5 years of follow-up. We conclude that in patients with CMT and a related cauda syndrome because of hypertrophic caudal nerve roots, acute decompression can be an effective and safe treatment with long-term efficacy.