Procalcitonin, a high acute phase reactant in antiepileptic hypersentivity syndrome in pediatric age
Verónica Cantarín-Extremera1, Cristina Castaño-De La Mota, Javier Alvarez-Coca
1Department of Pediatric Neurology, Hospital Infantil Universitario Niño Jesús, Avd. Menéndez Pelayo 65, 28009 Madrid, Spain. verocantarin@hotmail.com
Insights
Antiepileptic hypersensitivity syndrome (AHS) in children can be severe. This study reports the first pediatric cases of AHS with high procalcitonin (PCT) levels, highlighting its potential role in diagnosis.
Area of Science:
- Pediatric Medicine
- Clinical Immunology
- Pharmacology
Background:
- Antiepileptic hypersensitivity syndrome (AHS) is a severe condition in children, often linked to anticonvulsant drugs and antibiotics.
- While its pathogenesis remains unclear, AHS presents with diverse symptoms including skin reactions, fever, and lymphadenopathy, potentially affecting multiple organs.
- Elevated procalcitonin (PCT) has been noted in adult AHS cases, but its significance in pediatric AHS is less understood.
Observation:
- Laboratory findings in AHS can include leukocytosis, eosinophilia, and elevated transaminases.
- Significant procalcitonin (PCT) elevation has been noted in adult AHS cases.
- This report details two pediatric cases (14-year-old male, 13-year-old female) exhibiting AHS with markedly high PCT levels.
Findings:
- These represent the first documented cases of elevated procalcitonin in pediatric patients with Antiepileptic hypersensitivity syndrome.
- The findings suggest PCT may serve as a biomarker for AHS severity in children.
- The observed high PCT levels in pediatric AHS warrant further investigation.
Implications:
- Accurate diagnosis of AHS is crucial to prevent exposure to the causative agent.
- Prompt withdrawal of the implicated drug is the primary treatment for AHS.
- Systemic corticosteroids may be necessary for patients who do not improve or deteriorate after drug withdrawal.
Abstract:
Antiepileptic hypersensitivity syndrome (AHS) is a potentially life-threatening syndrome in pediatric cases. It is associated with aromatic anticonvulsivant drugs and others antibiotics with or without associated reactivation of virus. The pathogenesis of the process is not clear. Clinical feature of this syndrome include cutaneous reactions, fever and lymphadenopathies, but different organs can be involved. In laboratory analyses we can find leucocytosis, eosinophilia, and increase in transaminase levels. Significant elevation of procalcitonin (PCT) has been described in two adults patients. This study we report two cases of a 14-year-old male and a 13-year-old female with a AHS and a high level of the PCT. These are the first cases described in pediatric age. Establishing a diagnosis of AHS is important to avoid the use of the involved drug. The treatment is based on the withdrawal of the drugs that are supposed and if there is no improvement or a deterioration of the patient, the use of systemic corticosteroids is often useful.
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