JMCR: Highlight

Bronchiolitis Obliterans After Pediatric Toxic Epidermal Necrolysis An 11-year-old boy survived toxic epidermal necrolysis involving 80% of his body surface area, but progressive dyspnea revealed a rare and lasting complication: bronchiolitis obliterans.

Published in Biomedical Research

JMCR: Highlight

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The Case

An 11-year-old Chinese boy presented with fever, cough, oral mucosal erosion, rapidly progressive rash, and respiratory distress. Within five days, epidermal detachment involved approximately 80% of his body surface area, accompanied by extensive ocular, oral, and genital mucosal involvement.

The clinical findings supported toxic epidermal necrolysis, possibly triggered by Mycoplasma pneumoniae infection. He required invasive mechanical ventilation and received systemic glucocorticoids, intravenous immunoglobulin, plasma exchange, etanercept, antimicrobial therapy, and intensive skin, mucosal, and ophthalmologic care.

His acute illness stabilized, and the cutaneous lesions nearly completely re-epithelialized. However, persistent cough, exertional dyspnea, reduced exercise tolerance, and hypoxemia developed after discharge.

Chest computed tomography demonstrated bronchial wall thickening, diffuse hyperlucency, and mosaic attenuation. Bronchoscopy subsequently revealed extensive scarring, stenosis, membranous atresia, and fibrous obstruction of the peripheral airways, consistent with bronchiolitis obliterans.

Bronchoscopic holmium laser ablation was used to recanalize visible obstructed airways. Oxygen saturation and exercise tolerance improved, but severe irreversible airflow obstruction persisted at 21 months, with an FEV₁ of 27% predicted and an FEV₁/FVC ratio of 35%.

The child also developed severe illness-related anxiety requiring psychological counseling. He ultimately returned to full-time school and routine outdoor activities, although mild exertional dyspnea remained.

Why This Case Matters

Toxic epidermal necrolysis is principally recognized for its dramatic cutaneous and mucosal manifestations, but respiratory epithelial injury may lead to delayed and irreversible small-airway disease. Apparent cutaneous recovery should not be mistaken for complete systemic recovery.

Persistent cough, hypoxemia, exertional dyspnea, or reduced exercise tolerance after SJS/TEN should prompt evaluation for bronchiolitis obliterans, including pulmonary-function testing and expiratory chest imaging.

Although bronchoscopic holmium laser ablation was followed by symptomatic and functional improvement in this patient, the persistent severe spirometric impairment underscores the distinction between airway recanalization and reversal of established bronchiolar fibrosis. A single case cannot establish the efficacy or safety of this intervention.

Clinical Take-Home Message

Children recovering from severe toxic epidermal necrolysis require prolonged multidisciplinary surveillance. New or persistent respiratory symptoms should trigger early assessment for bronchiolitis obliterans, even after the skin and mucosal lesions have healed. Long-term care should address both irreversible organ dysfunction and the psychological consequences of critical illness.

Article: Duan G, Chen J, Li C. Toxic epidermal necrolysis complicated by bronchiolitis obliterans in a child: a case report. Journal of Medical Case Reports. 2026.
DOI: 10.1186/s13256-026-06572-0

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