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Granulomatous Inflammation Causing Severe Supraglottic Edema and Airway Obstruction in a Pediatric Patient
Sophia M Colevas1, Bradley T Gietman1, Shelly M Cook2
1Division of Otolaryngology-Head and Neck Surgery, Department of Surgery, 5232University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Insights
A pediatric patient with sleep-disordered breathing had chronic granulomatous swelling of the supraglottic larynx. Management included airway support and laryngeal procedures, leading to decannulation.
Area of Science:
- Otolaryngology
- Pediatric Gastroenterology
- Pulmonology
Background:
- Inflammatory bowel disease (IBD), particularly Crohn disease (CD), can manifest in the upper airway.
- Laryngeal involvement in pediatric CD is rare, with limited case reports available.
- Granulomatous inflammation of the supraglottic larynx presents diagnostic and management challenges.
Observation:
- A 12-year-old male with a family history of IBD presented with sleep-disordered breathing.
- Examination revealed chronic, granulomatous supraglottic laryngeal swelling.
- The patient underwent tracheostomy, laryngeal steroid injections, supraglottoplasty, and CO2 laser resurfacing.
Findings:
- The patient was successfully decannulated after multidisciplinary airway management.
- Differential diagnoses included Crohn disease and laryngeal sarcoidosis due to non-necrotic granulomatous inflammation.
- This case highlights the rarity of laryngeal CD in pediatric patients (2 of 13 reported cases).
Implications:
- This case adds to the limited literature on pediatric laryngeal manifestations of Crohn disease.
- Effective management strategies for supraglottic edema with unclear etiology are discussed.
- Early recognition and intervention are crucial for managing airway compromise in pediatric IBD.
Abstract:
A 12-year-old male with a family history of inflammatory bowel disease presented with sleep-disordered breathing and was found to have chronic, granulomatous swelling of the supraglottic larynx. His airway was managed with tracheostomy, regular interval laryngeal steroid injections, supraglottoplasty, and "pepper pot" CO2 laser resurfacing leading to eventual decannulation. Due to the non-necrotic nature of the granulomatous inflammation, as well as the patient's family history of inflammatory bowel disease, the leading diagnosis was Crohn disease, but isolated laryngeal sarcoidosis could not be ruled out. There are only 13 reported cases of laryngeal manifestations of Crohn disease in the literature, with only 2 cases occurring in pediatric patients. This case report adds to this body of literature and discusses strategies for managing granulomatous supraglottic edema when definitive diagnosis is not fully clear.
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