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Published on: September 20, 2018
Coma blisters in children: case report and review of the literature
Laura Bosco1, Donatella Schena, Chiara Colato
11Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy.
Insights
Coma-induced blisters, a rare skin condition, can occur in children with severe neurological impairment like meningoencephalitis. This case highlights the importance of clinical-pathologic correlation for accurate diagnosis in pediatric patients.
Area of Science:
- Pediatric Dermatology
- Neurology
- Pathology
Background:
- Coma-induced blisters (coma bullae) are a rare phenomenon typically associated with drug overdose in adults.
- Limited pediatric cases of coma bullae have been documented, making this condition poorly understood in children.
Observation:
- A case report details an 11-year-old child experiencing coma bullae secondary to meningoencephalitis.
- The bullous lesions appeared on the trunk and limbs, progressing to necrotic ulcers.
- No drug overdose was identified as the cause in this pediatric patient.
Findings:
- Skin biopsy revealed epidermal and eccrine sweat gland necrosis with neutrophilic infiltration.
- Dermal vessel thrombosis was observed, suggesting a vascular component.
- Literature review confirmed only five previously reported pediatric cases of coma bullae.
Implications:
- This case expands the understanding of coma bullae in pediatric populations, particularly in the context of non-overdose-related neurological conditions.
- Accurate diagnosis requires distinguishing coma bullae from other pediatric blistering disorders through clinical and pathological evaluation.
- Coma bullae demonstrate spontaneous resolution, emphasizing supportive care and accurate diagnosis.
Abstract:
Coma-induced blisters is a rare condition associated with prolonged impairment of conscious level, which is relatively well-known in adults following overdose with barbiturates. However, it has been very rarely described in children. A case of coma-bullae occurring in an 11-year-old child with meningoencephalitis is herein reported. The bullous lesions occurred on the limbs and trunks, and evolved into necrotic ulcers in a few days. No correlation with any drug overdosage was found. A skin biopsy revealed epidermal and eccrine sweat gland necrosis with abundant neutrophils, and thrombosis of the vessels in the lower dermis. A comprehensive review of the literature showed that only 5 cases of coma-bullae in children have been published so far. Coma blistering resolves spontaneously within days or weeks. Diagnosis of coma-bullae may require careful clinical-pathologic correlation to exclude other blistering diseases in children.
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