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Langerhans cell histiocytosis is a rare disorder in children that can involve the head and neck, may mimic common ENT conditions and delay diagnosis. While various case reports exist, ENT-focused reviews remain limited.
Methods
We conducted a literature review of 73 studies encompassing 244 paediatric patients with head and neck Langerhans cell histiocytosis, extracting data on presentation, treatment and outcomes. We also present a retrospective case series of 25 patients treated at a single tertiary institution.
Results
Otologic and craniofacial bone involvement were the most common presentations. Treatments ranged from surgical curettage and intra-lesional steroids to systemic chemotherapy. Recurrence was more common in multifocal and multisystem disease. Our institutional series supported many of these findings, with detailed follow-up data and treatment responses.
Conclusion
This is the most extensive ENT-focused review of paediatric Langerhans cell histiocytosis to date. It highlights key clinical patterns and management approaches to aid early recognition and tailored treatment.
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