A 45-year-old man, who had taken carbamazepine for a month to treat glossopharyngeal neuralgia, presented with fever and itchy eruption. At his first visit, he had generalized erythema with periocular sparing, swelling of cervical lymph nodes and liver dysfunction. Histopathology of the skin lesion revealed epidermal spongiosis, liquefaction degeneration of the basal layer and edema and inflammatory infiltrates in the dermis, which are seen in erythema exsudativum multiforme. Carbamazepine was discontinued, and he was treated with 30mg/day of prednisolone. As skin rash and liver dysfunction were improved, prednisolone dose was tapered slowly and 80 days after, treatment was completed. Patch testing for carbamazepine was positive, but a drug-induced lymphocyte stimulation test for the drug was negative. Reactivation of human herpesvirus 6, 7, cytomegalovirus or Epstein-Barr virus was not detected during the course of his disease. Based on these findings, atypical type of drug-induced hypersensitivity syndrome (DIHS) due to carbamazepine was diagnosed. After improvement of DIHS, he had depressive and suicidal thoughts. He consulted a psychiatrist and depressive state was diagnosed. Antidepressants relieved his symptoms in three months. We should be aware of psychiatric symptoms associated with DIHS, even after improvement of skin conditions, although our case may be rare.Skin Research, 16: 129-132, 2017
View full abstract