Laryngeal cleft - A diagnostic and treatment challenge

Authors

  • Ana Brett Interna de Formação Específica em Pediatria Médica do Hospital Pediátrico de Coimbra, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal
  • Teresa Dionísio Assistente Hospitalar do Serviço de Cuidados Intensivos Pediátricos, Hospital Pediátrico de Coimbra, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal
  • Leonor Carvalho Assistente Hospitalar Graduada de Pediatria, Serviço de Cuidados Intensivos Pediátricos, Hospital Pediátrico de Coimbra, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal
  • Miguel Félix Assistente Hospitalar Graduado de Pediatria, Serviço de Pediatria Médica, Hospital Pediátrico de Coimbra, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal
  • Felisberto Maricato Assistente Hospitalar Graduado de Otorrinolaringologia, Serviço de Otorrinolaringologia, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal
  • Guri Sandhu Consultant Otolaryngologist and Head & Neck Surgeon, Department of Paediatric Respiratory Medicine, Royal Brompton & Harefield NHS Foundation Trust, London, United Kingdom
  • Farela Neves Chefe de Serviço do Serviço de Cuidados Intensivos Pediátricos, Hospital Pediátrico de Coimbra, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal

DOI:

https://doi.org/10.34631/sporl.11

Keywords:

esophageal atresia, laryngeal cleft, microlaryngoscopy under anesthesia, endoscopic treatment

Abstract

Laryngeal clefts are a rare, underdiagnosed, with variable severity but potentially fatal disease. We report the case of an infant submitted on his first day of life to surgical repair of long hiatus oesophageal atresia with associated tracheoesophageal fistula. At 26 days of life he began enteral feeding by mouth, presenting six days later, whilst feeding, with an episode of dessaturation and extreme bradycardia which required resuscitation. Frequent episodes of rough breathing, similar to a snort, associated with crying were noticed. Laryngotracheal bronchoscopy showed changes in the anatomy of the larynx. Microlaringoscopy under anaesthesia confirmed a laryngeal cleft extending beyond the cricoid cartilage (type III). He underwent tracheostomy and endoscopic laryngeal cleft repair at three months of life, with good outcome. In these clinical situations, a high index of suspicion is warranted as early diagnosis allows for better survival.

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How to Cite

Brett, A., Dionísio, T., Carvalho, L., Félix, M., Maricato, F., Sandhu, G., & Neves, F. (2013). Laryngeal cleft - A diagnostic and treatment challenge. Portuguese Journal of Otorhinolaryngology and Head and Neck Surgery, 51(1), 57–60. https://doi.org/10.34631/sporl.11

Issue

Section

Case Report