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Ganglioneuroblastoma Presenting as Obstructive Sleep Apnea in a 5-Year-Old Boy
Aaron Wallace1, Gabe Kaufmann2, Nishant Agrawal1
1Department of Surgery, Section of Otolaryngology-Head and Neck Surgery, University of Chicago.
Insights
A rare ganglioneuroblastoma caused severe obstructive sleep apnea (OSA) in a child. Surgical removal of the sympathetic chain tumor resolved the patient's OSA, highlighting a critical diagnostic consideration.
Area of Science:
- Pediatric Oncology
- Sleep Medicine
- Otolaryngology
Background:
- Ganglioneuroblastomas are rare tumors originating from the sympathetic nervous system.
- Obstructive sleep apnea (OSA) in children can have various causes, including anatomical obstruction.
Observation:
- A healthy 5-year-old boy presented with severe obstructive sleep apnea (apnea-hypopnea index of 86 events/hour).
- Initial investigations, including adenotonsillectomy, did not resolve the severe OSA.
- Further evaluation revealed a large pharyngeal mass, later identified as ganglioneuroblastoma.
Findings:
- The ganglioneuroblastoma, a tumor of the sympathetic chain, was compressing the airway.
- Surgical excision of the tumor led to a complete resolution of the patient's obstructive sleep apnea.
Implications:
- This case underscores the importance of considering rare tumors in the differential diagnosis of pediatric obstructive sleep apnea, especially when typical causes are ruled out.
- Early diagnosis and surgical intervention are crucial for managing airway compromise caused by such tumors.
- Highlights the multidisciplinary approach required for diagnosing and treating complex pediatric airway conditions.
Abstract:
The authors present an interesting case of ganglioneuroblastoma, a tumor of the sympathetic chain, presenting as severe obstructive sleep apnea in a healthy 5-year-old boy. The patient's initial polysomnogram demonstrated an apnea-hypopnea index (AHI) of 86 events/hour. He underwent an adenotonsillectomy at an outside hospital and his repeat AHI was still 62. The patient was nonobese and nonsyndromic appearing, which made his incredibly high AHI perplexing. He underwent sleep endoscopy and direct laryngoscopy for further evaluation, which demonstrated a large mass in the left posterior pharynx. He then underwent surgical excision with a resolution of his obstructive sleep apnea.
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