Acute visual dysfunction following phenytoin-induced toxicity.
نویسندگان
چکیده
PURPOSE To report that acute phenytoin toxicity may result in acute visual dysfunction. METHODS A 19-year old man with cryptogenic simple partial and secondary generalized epilepsy developed blurred vision and xanthopsia after phenytoin loading for status epilepticus. Color blindness was found on testing with Ishihara's pseudo-isochromatic charts and visual fields (Goldmann perimeter) showed gross concentric constriction in both eyes. Flash visually evoked potentials showed prolonged P1 latency in both the eyes. Serum free-phenytoin concentration revealed toxic levels of phenytoin and no other etiology for retinopathy or optic neuropathy. RESULTS Phenytoin was withheld and the patient experienced a partial recovery in conjunction with reduced serum levels of phenytoin. Ten months later flash visually evoked potentials were normal but electroretinogram confirmed diffuse bilateral cone and rod dysfunction. CONCLUSION Phenytoin toxicity may result in acute visual dysfunction a previously unreported phenomenon.
منابع مشابه
Treatment of Acute Tacrolimus Toxicity with Phenytoin in Solid Organ Transplant Recipients
The pharmacokinetics of tacrolimus are influenced by many factors, including genetic variability, acute infections, liver dysfunction, and interacting medications, which can result in elevated concentrations. The most appropriate management of acute tacrolimus toxicity has not been defined though case reports exist describing the therapeutic use of enzyme inducers to increase tacrolimus metabol...
متن کاملPersistent cerebellar ataxia with cerebellar cognitive affective syndrome due to acute phenytoin intoxication: A case report
Phenytoin is one of the commonly used antiepileptic drugs. The common dose dependent and reversible neurological side effects of phenytoin are nystagmus, diplopia, dysarthria, ataxia, incoordination, chorioathetosis, orofacial dyskinesias and drowsiness. Persistent cerebellar dysfunction with cerebellar atrophy is a well known complication of long term phenytoin use. There are several mechanism...
متن کاملTrimethoprim/sulfamethoxazole-induced phenytoin toxicity in the elderly: a population-based study.
AIMS Pharmacokinetic studies suggest that trimethoprim (TMP) can inhibit the hepatic metabolism of phenytoin, but the clinical relevance of this is uncertain. We studied the risk of phenytoin toxicity following the prescription of trimethoprim/sulfamethoxazole (TMP/SMX), a commonly used antibiotic, among elderly patients receiving phenytoin. METHODS We conducted a population-based, nested cas...
متن کاملIn-vitro lymphocyte toxicity to a phenytoin metabolite in phenytoin induced cutaneous adverse drug eruptions.
BACKGROUND Phenytoin, one of the most commonly used antiepileptic drug, is associated with a wide spectrum of adverse drug eruptions. It is metabolized by the hepatic microsomal enzymes. The intermediate metabolites are arene oxides which accumulate due to deficiency of the enzyme epoxide hydrolase. These are postulated to be associated with phenytoin induced hepatotoxicity and antiepileptic hy...
متن کاملMitochondrial Toxicity of Depleted Uranium: Protection by Beta-Glucan
Considerable evidence suggests that mitochondrial dysfunction contributes to the toxicity of uranyl acetate (UA), a soluble salt of depleted uranium (DU). We examined the ability of the two antioxidants, beta-glucan and butylated hydroxyl toluene (BHT), to prevent UA-induced mitochondrial dysfunction using rat-isolated kidney mitochondria. Beta-glucan (150 nM) and BHT (20 nM) attenuated UA-indu...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Acta neurologica Belgica
دوره 103 4 شماره
صفحات -
تاریخ انتشار 2003