|Year : 2011 | Volume
| Issue : 1 | Page : 13-15
Oxcarbazepine-induced Stevens Johnson syndrome: A rare case report
SR Sharma, Nalini Sharma, ME Yeolekar
Department of Neurology, NEIGRIHMS, North Eastern Indira Gandhi Regional Institute of Medical Sciences, Shillong, India
|Date of Web Publication||21-Apr-2011|
S R Sharma
Department of Neurology, NEIGRIHMS, North Eastern Indira Gandhi Regional Institute of Medical Sciences, Shillong
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Although carbamazepine is the most common cause of Stevens Johnson syndrome (SJS) a new antiepileptic drug, oxcarbazepine which is structurally related to carbamazepine, has also been rarely shown to induce SJS. Here we report a case with SJS, which was induced by oxcarbazepine.
Keywords: Oxcarbazepine, Solitary small enhancing computerized tomography lesion, Stevens-Johnson syndrome
|How to cite this article:|
Sharma S R, Sharma N, Yeolekar M E. Oxcarbazepine-induced Stevens Johnson syndrome: A rare case report. Indian Dermatol Online J 2011;2:13-5
|How to cite this URL:|
Sharma S R, Sharma N, Yeolekar M E. Oxcarbazepine-induced Stevens Johnson syndrome: A rare case report. Indian Dermatol Online J [serial online] 2011 [cited 2020 Feb 22];2:13-5. Available from: http://www.idoj.in/text.asp?2011/2/1/13/79861
| Introduction|| |
Stevens-Johnson syndrome More Details (SJS) and toxic epidermal necrolysis (TEN), defined by widespread blisters arising on macules and/or flat atypical targets are diseases with homogenous clinical characteristics and a potentially lethal outcome.  SJS is usually associated with several antiepileptic drugs including carbamazepine, lamotrigine, phenobarbital, phenytoin, and valproic acid.  A new antiepileptic oxcarbazepine, which is structurally related to carbamazepine (CBZ), was introduced for use in patients with epilepsy. First synthesized in 1966, it was eventually approved for use as an anticonvulsant in EU countries and India in 1999.
According to a review of the literature, it appears that oxcarbazepine-induced SJS has rarely been reported.  Here we report a rare case of oxcarbazepine-induced SJS.
| Case Report|| |
A 21-year old male presented with two episodes of right parietal with secondary generalized epilepsy since 2 weeks. Physical examination showed unremarkable findings. CT scan of head with contrast revealed left parietal lobe solitary small enhancing computerized tomography lesion (SSECTL) with mild edema. Electroencephalography (EEG) showed normal awake recordings. He was treated with oxcarbazepine 300 mg twice a day which was gradually titrated to 600 mg twice a day within a week. The patient developed high fever and multiple maculopapular eruptions [Figure 1], [Figure 2] and [Figure 3] were found over the patient's face and trunk around the 14 th day of taking oxcarbazepine. Two to three days later, some blisters were also observed on his upper extremities. This way s followed b multiple oral ulcers and hyperemic conjunctivae.
|Figure 1: Targetoid rashes over both upper extremities, conjuctiva and oral mucosa in resolution after 2 weeks of treatment|
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|Figure 2: Targetoid rashes over both lower extrimities, 2 weeks of oxz initiation|
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He was admitted in neurology ward with the help of dermatologist with the diagnosis of SJS. Laboratory investigations showed leucocytosis (WBC, 14630/l, reference value, 4000-11 000/l) and elevated C-reactive protein 60.78 g/ml; reference range, 0-5 g/Ml.
A skin biopsy was also performed to confirm histopathology.
The stratum corneum layer appeared to be normal. There was marked liquefactive degeneration with some dyskeratotic keratinocytes. The dermis showed lymphohistiocytic infiltration around blood vessels and scanty eosinophils. The skin pathology was consistent with SJS.
| Discussion|| |
The diagnosis of SJS is based on clinical manifestations with acute onset of rapidly expanding targetoid erythematous macules, necrosis and detachment of the epidermis along with erythema, erosions, and crusting of two or more mucosal surfaces.  Oxcarbazepine, the incriminated drug in this case was first synthesized in 1966,was approved for use as an anticonvulsant in Denmark in 1990,was approved in Spain in 1993, in Portugal in 1997, and eventually for all other EU countries and in India in 1999. It was approved in the US in 2000.
The patients usually develop a hypersentivity reaction to this drug between 2 and 12 weeks after commencing treatment with it.  Our patient had targetoid erythematous eruptions and mucosal involvement 2 weeks after starting oxcarbazepine treatment. During these 2 weeks he took no medicine except for oxcarbazepine. The skin pathology finding revealed lymphohistiocytic infiltration around the blood vessels and scanty eosinophils, which was consistent with SJS.
In this case, we used 300 mg of oxcarbazapine twice daily for seizure control and then increased the dose to 600 mg twice daily. Both the initial and titration doses were slightly lower than the recommended doses. It has been reported that higher daily doses of drugs are associated with increased risk of SJS just as is the case for allopurinol.  However, there is no evidence about the relationship between oxcarbazepine dosage and SJS.
Although many factors have been proposed as risk factors of SJS including adverse drug effects, malignant disorders or graft-host disease and infections, most of them were induced by drugs. The most common drugs are anticonvulsants, particularly carbamazepine.(CBZ).  To our knowledge, there are no reports of oxcarbazepine-induced SJS from India. According to the Food and Drug Administration the incidence of oxcarbazepine-induced SJS is estimated to range between 0.5 and 6 cases per million people per year within general population.  The incidence of carbamazepine-induced SJS is higher than that for oxcarbazepine induced SJS. The reason why oxcarbazepine has fewer side effect is that oxcarbazepine is almost completely metabolized through reduction and conjugation to yield an active monohydroxy derivative. In contrast, the oxidation of CBZ to 10, 11-epoxide is regarded as the most common cause of adverse effects.  The pathogenesis of SJS remains unclear and there is considerable debate whether to treat SJS with systemic steroids. However, Lam et al, found that the early use of short-term systemic steroids for 3-5 days lacked any significant side effects and did not increase mortality or morbidity in children.  Our patient was treated with intravenous steroid and antihistamine for 7-9 days. His condition improved and he was discharged 14 days after admission. No sequelae were found during 2 months of follow-up.
In conclusion, we have described perhaps the first case of oxcarbazepine-induced SJS in India. We need to recruit more patients to elucidate the pathogenesis of oxcarbazepine-induced SJS.
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[Figure 1], [Figure 2], [Figure 3]