Type I Chiari malformation presenting central sleep apnea

Auris Nasus Larynx. 2014 Apr;41(2):222-4. doi: 10.1016/j.anl.2013.07.011. Epub 2013 Oct 23.

Abstract

Sleep apnea is a rare but a well-known clinical feature of type I Chiari malformation. It may be obstructive or central in nature. Sleep apnea in patients with type I Chiari malformation rarely presents without accompanying neurological signs or symptoms. We here report a case of a 10-year-old girl who presented with central sleep apnea without any other neurological signs but was ultimately diagnosed with type I Chiari malformation. The patient initially showed mild improvement in symptoms after administration of an acetazolamide. Finally, posterior fossa decompression dramatically improved her respiratory status during sleep, both clinically and on polysomnography. This case suggests that type I Chiari malformation should be considered in the differential diagnoses of central apneas in children, even if there are no other neurological signs and symptoms. Furthermore, sagittal craniocervical magnetic resonance imaging may be necessary for a definitive diagnosis.

Keywords: Acetazolamide; Central sleep apnea; Children; Polysomnography; Type I Chiari malformation.

Publication types

  • Case Reports

MeSH terms

  • Acetazolamide / therapeutic use
  • Arnold-Chiari Malformation / complications
  • Arnold-Chiari Malformation / diagnosis*
  • Arnold-Chiari Malformation / therapy
  • Carbonic Anhydrase Inhibitors / therapeutic use
  • Child
  • Decompression, Surgical / methods
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Polysomnography
  • Sleep Apnea, Central / diagnosis*
  • Sleep Apnea, Central / etiology
  • Sleep Apnea, Central / therapy

Substances

  • Carbonic Anhydrase Inhibitors
  • Acetazolamide