|Year : 2012 | Volume
| Issue : 1 | Page : 44-45
Stevens-Johnson syndrome induced by sodium valproate monotherapy
KN Naveen1, JS Arunkumar2, K Hanumanthayya1, VV Pai1
1 Department of Dermatology, Shri Dharamasthala Manjunatheshwara College of Medical Sciences and Hospital, Sattur, Dharwad - 580 009, India
2 Department of ENT, Shri Dharamasthala Manjunatheshwara College of Medical Sciences and Hospital, Sattur, Dharwad - 580 009, India
|Date of Web Publication||11-Apr-2012|
K N Naveen
Department of Dermatology, Shri Dharamasthala Manjunatheshwara College of Medical Sciences and Hospital, Sattur, Dharwad - 580 009
Source of Support: None, Conflict of Interest: None
| Abstract|| |
A case of Stevens-Johnson syndrome following treatment with sodium valproate is presented here. A 20-year-old male was put on sodium valproate monotherapy for the migraine, with generalized epilepsy. He developed vesicles and bullae in the oral and nasal mucosa with conjunctivitis, after 10 days of treatment. The lesions resolved after treating with systemic steroids. This case has been presented because Stevens-Johnson syndrome with sodium valproate monotherapy has been very rarely reported.
Keywords: Side effect, Stevens-Johnson syndrome, valproate
|How to cite this article:|
Naveen K N, Arunkumar J S, Hanumanthayya K, Pai V V. Stevens-Johnson syndrome induced by sodium valproate monotherapy. Int J Crit Illn Inj Sci 2012;2:44-5
|How to cite this URL:|
Naveen K N, Arunkumar J S, Hanumanthayya K, Pai V V. Stevens-Johnson syndrome induced by sodium valproate monotherapy. Int J Crit Illn Inj Sci [serial online] 2012 [cited 2020 Jul 14];2:44-5. Available from: http://www.ijciis.org/text.asp?2012/2/1/44/94904
| Introduction|| |
Sodium valproate is a broad-spectrum antiepileptic that has proven efficacy against all seizure types, which makes it a useful antiepileptic when the exact seizure classification is unknown or multiple seizure-types exists.  The aromatic antiepileptics, namely, phenytoin, carbamazepine, phenobarbitone, and primidone can cause hypersensitivity reactions.  For example, carbamazepine can cause pruritic and erythematous rashes, urticaria, photosensitivity reactions, exfoliative dermatitis, alopecia, diaphoresis, erythema multiforme, Stevens-Johnson syndrome More Details (SJS), and Toxic epidermal necrolysis (TEN).  In such a case carbamazepine is discontinued and nonaromatic antiepileptics like sodium valproate or a benzodiazepine is usually recommended as an alternative therapy.  The common side effects of valproate include anorexia, nausea, vomiting, sedation, ataxia, tremor, alopecia, stimulation of appetite, elevation of hepatic transaminases, and rarely fulminant hepatitis.  Stevens-Johnson syndrome is rarely reported with it.  In most of the reported cases of SJS due to valproate, it has been found when it is given with other drugs. ,, SJS due to valproate monotherapy is rarely reported.
We present a case of Stevens-Johnson syndrome due to valproate monotherapy.
| Case Report|| |
A 20-old-medical student had a past medical history of migraine and generalized seizures, with postictal visual and auditory hallucinations, for which sodium valproate 900 mg was prescribed. His baseline investigations, such as, liver function and complete hemogram were within normal limits. After seven days he developed fever with myalgia, followed by lesions in the oral cavity two days later. He also had difficulty in swallowing. On examination there were erosions in the oral and nasal mucosa [Figure 1]. Conjunctivitis was present. Tzank smear was negative. There were hemorrhagic crusts on his lips [Figure 2]. There were no skin lesions. No genital or anal involvement. No arthritic features. His complete hemogram, liver function tests, and chest X-ray, were within normal limits. His HIV and HbsAg status were negative. Sodium valproate was withdrawn and he was started on systemic steroids and antihistaminics. The lesions resolved within a few days.
| Discussion|| |
The Stevens-Johnson syndrome and Toxic epidermal necrolysis are rarely reported side effects of valproate. ,,, Rzany et al, in a case control study on the risk of SJS and TEN with various anti-epileptic agents, reported the univariate relative risk as, 120 for carbamazepine, 91 for phenytoin, 57 for Phenobarbital, 25 for lamotrigine, and 24 for valproate within the first eight weeks of therapy. The association of SJS with valproate was confounded by concomitant short-term therapy with other casual drugs in many studies.  Roujeau et al, conducted a case control study to quantify the risks associated with the use of specific drugs. Drug use before the onset of disease was compared in 245 people who were hospitalized because of TEN or SJS and 1147 patients hospitalized for other reasons. The crude relative risk for SJS or TEN was as follows: carbamazepine, 90; phenytoin, 53; Phenobarbital, 45, and valproic acid, 25. 
Suresh Kumar PN et al, reported a case of SJS after he was put on sodium valproate 600 mg per day, haloperidol 10 mg per day, and trihexiphenidyl 4 mg per day, which resolved after withdrawing sodium valproate and putting him on systemic steroids. 
In most of the studies, SJS was caused by valproate, when it was used in combination with other drugs. ,, In our case SJS was found with valproate monotherapy and was limited only to the mucosa. There was no skin involvement. This case is presented because valproate monotherapy-induced SJS is rarely reported.
| Conclusion|| |
As sodium valproate may also cause Stevens-Johnson syndrome, one should be careful while initiating therapy with valproate.
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[Figure 1], [Figure 2]