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387 Hypersensitivity Syndrome Associated with Phenytoin Sodium

BACKGROUND: The drug-induced hypersensitivity syndrome (DIHS) is a systemic reaction for drug-induced idiosyncratic. We report 1 in 1000 to 1 in 10,000 exposures to aromatic anticonvulsant. In the case of phenytoin is estimated at 2.3 to 4.5 per 10,000 exposures. There is a deficit of microsomal epo...

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Detalles Bibliográficos
Autor principal: Mendieta, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Allergy Organization Journal 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3513021/
http://dx.doi.org/10.1097/01.WOX.0000412150.57661.b2
Descripción
Sumario:BACKGROUND: The drug-induced hypersensitivity syndrome (DIHS) is a systemic reaction for drug-induced idiosyncratic. We report 1 in 1000 to 1 in 10,000 exposures to aromatic anticonvulsant. In the case of phenytoin is estimated at 2.3 to 4.5 per 10,000 exposures. There is a deficit of microsomal epoxide hydroxylase causing accumulation of toxic metabolites. Occurs between 2 weeks to 3 months after drug exposure; it is characterized by maculopapular rash, erythema midface, fever, lymphadenopathy, with alteration of the hematologic system with eosinophilia, peripheral or atypical lymphocytosis. Described reactivation of herpes virus (HHV-6 and 7). Comorbidities during the syndrome such as type 1 diabetes, encephalitis, and long-term sequelae such as thyroid dysfunction, systemic lupus erythematosus, etc.1 METHODS: We report a 39 year old female with history of traumatic brain injury (TBI) received proflaxis with phenytoin sodium 100 mg 1vo c/8 hours, 4 weeks after starting with fever, malaise, sore throat, cervical lymphadenopathy, appeared itchy rash in face, neck. Admitted with malaise, generalized rash, edema midface, cheilitis, jaundice, cervical lymphadenopathy, axillary and inguinal and hepatomegaly. We continued to study probable hypersensitivity syndrome asking paraclinical studies including blood count, liver function tests. We initiated 1 mg/kg/d prednisone for 6 weeks and subsequent dose reduction. Exit after 5 days of hospitalization for clinical improvement. Continuous current monitoring by the outpatient department of our hospital and late complications that can occur in this syndrome. RESULTS: Liver function tests as well as the count of the white series was abnormal, with the following report: AST (177 U/L), ALT (154 U/L), WBC (12.430 mm(3)), eosinophil (1.310 mm(3)). Biopsy report unavailable. CONCLUSIONS: Aromatic anticonvulsants (phenytoin, carbamazepine and phenobarbital) are frequent causes of DIHS. Treatment involves discontinuation of the drug involved, admission to intensive care and systemic steroids at doses of 0.5 to 1 mg/kg/d and intravenous immunoglobulin 2 g/kg.