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Recurrent respiratory papillomatosis in children: masquerader of common respiratory diseases
Michael C Zacharisen1, Stephen F Conley
1Department of Pediatrics, Section of Allergy and Immunology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA. mzach@mcw.edu
Insights
Recurrent respiratory papillomatosis (RRP) in children is a rare airway tumor. Early diagnosis via laryngoscopy is crucial, especially when common pediatric conditions do not respond to treatment.
Area of Science:
- Pediatric Otolaryngology
- Pediatric Pulmonology
- Respiratory Oncology
Background:
- Recurrent respiratory papillomatosis (RRP) is an uncommon, potentially life-threatening benign tumor affecting the pediatric respiratory tract, primarily the larynx.
- Diagnosis can be challenging due to variable presentations and requires a high index of suspicion.
Observation:
- A series of case reports illustrate the varied presentations of RRP in children.
- Five pediatric patients (ages 2-6) were initially misdiagnosed with common conditions like croup, asthma, laryngeal hemangioma, and tracheomalacia.
Findings:
- Misdiagnosed patients presented with chronic dyspnea, cough, stridor, dysphonia, weak cry, and syncope.
- Prompt diagnosis led to surgical ablation of papillomata for RRP management.
Implications:
- Flexible fiber-optic laryngoscopy is recommended for any child with voice disturbance and/or stridor.
- Consider RRP in pediatric patients whose symptoms deviate from the typical course or treatment response of common airway diseases.
Background:
Recurrent respiratory papillomatosis in children is an uncommon but potentially life-threatening benign tumor of the respiratory tract with laryngeal predilection. The diagnosis of recurrent respiratory papillomatosis may be challenging unless there is a high index of suspicion and awareness of the variable presentations.
Methods:
We reviewed the medical charts of children with recurrent respiratory papillomatosis treated at a tertiary children's hospital. The presentation of recurrent respiratory papillomatosis is illustrated by a series of case reports. We provide a paradigm to assist in the early diagnosis of children with recurrent respiratory papillomatosis.
Results:
Five patients, aged 2 to 6 years, were erroneously diagnosed with recurrent croup, asthma, laryngeal hemangioma, and tracheomalacia after presenting with variable degrees of chronic dyspnea, cough, stridor, dysphonia, weak cry, and syncope. Once the diagnosis of recurrent respiratory papillomatosis was made, recurring surgical ablation of papillomata was initiated.
Conclusions:
Any child presenting with a voice disturbance with or without stridor is recommended to have diagnostic flexible fiber-optic laryngoscopy. Recurrent respiratory papillomatosis should be considered in children when other common pediatric airway diseases either do not follow the natural history or do not respond to treatment of the common disorder.
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