Fenniche S, Dhaoui A, Ammar F Ben, Benmously R, Marrak H, Mokhtar I
Dermatology Department, Habib Thameur Hospital, Tunis, Tunisia.
Skin Pharmacol Physiol. 2005 Sep-Oct;18(5):230-3. doi: 10.1159/000086668. Epub 2005 Jul 5.
Beta-blocking medications are rarely associated with drug-induced lupus erythematosus syndrome and have never been incriminated as a cause of subacute lupus erythematosus (SCLE). We present herein the first case of SCLE induced by acebutolol. A 57-year-old woman presented with a 1-month history of a cutaneous eruption of the photo-exposed areas. One month ago, the patient had started a treatment with oral acebutolol to cure a hypertension of 1-year evolution. Physical examination revealed erythematous scaly annular plaques, involving the face, arms and trunk. Immunologic serology findings revealed a positive titer of antinuclear antibodies up to 1/1,280 with positivity of antihistone and Ro/SSA antibodies. Acebutolol was stopped, and the lesions cleared completely 4 months later. Literature data, along with our case, suggest a link between acebutolol therapy and the onset of a lupus syndrome. Although this is the first report of acebutolol-induced SCLE, we should be aware of this occurrence, and avoidance of acebutolol is recommended in patients with stigmata of lupus erythematosus.
β受体阻滞剂很少与药物性红斑狼疮综合征相关,且从未被认定为亚急性皮肤型红斑狼疮(SCLE)的病因。我们在此报告首例由醋丁洛尔诱发的SCLE病例。一名57岁女性,有1个月光暴露部位皮肤发疹的病史。1个月前,该患者开始口服醋丁洛尔治疗病程长达1年的高血压。体格检查发现面部、手臂和躯干出现红斑鳞屑性环状斑块。免疫血清学检查结果显示抗核抗体滴度阳性高达1/1280,抗组蛋白抗体和Ro/SSA抗体阳性。停用醋丁洛尔后,皮损在4个月后完全消退。文献数据以及我们的病例表明醋丁洛尔治疗与狼疮综合征的发生之间存在关联。尽管这是首例醋丁洛尔诱发SCLE的报告,但我们应注意到这种情况,对于有红斑狼疮体征的患者,建议避免使用醋丁洛尔。