A bizarre case of accessory larynx in an infant with OEIS syndrome

Int J Pediatr Otorhinolaryngol. 2018 Nov:114:134-137. doi: 10.1016/j.ijporl.2018.08.037. Epub 2018 Aug 31.

Abstract

We report a bizarre case of accessory larynx in an infant with OEIS syndrome (omphalocele, cloacal exstrophy, imperforated anus & spinal defects). This is the first reported case in literature of a duplicate accessory larynx which is a mirror image of the true larynx. A congenital duplication of the larynx is a rare anomaly and can present in various forms. In this case, the infant presented with recurrent lung infection and inability to wean off oxygen. Scope revealed severe laryngomalacia in addition to the accessory larynx. Hence, supraglottoplasty was done with aim to resolve the lung and airway problem.

Keywords: Accessory larynx; Airway management; Congenital laryngeal abnormalities; Duplicate larynx; OEIS syndrome.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple
  • Anus, Imperforate / complications*
  • Female
  • Hernia, Umbilical / complications*
  • Humans
  • Infant, Newborn
  • Laryngeal Diseases / complications
  • Laryngeal Diseases / diagnosis*
  • Laryngeal Diseases / surgery
  • Laryngoscopy / methods
  • Larynx / abnormalities*
  • Larynx / surgery
  • Respiratory Sounds / etiology
  • Scoliosis / complications*
  • Urogenital Abnormalities / complications*

Supplementary concepts

  • Omphalocele exstrophy imperforate anus