Lemmenmeier Eva, Gaus Barbara, Schmid Patrick, Hoffmann Matthias
Division of Infectious Diseases and Hospital Hygiene, Cantonal Hospital St.Gallen, Rorschacherstrasse 95, 9007, St.Gallen, Switzerland.
Department of Dermatology, Cantonal Hospital St.Gallen, Rorschacherstrasse 95, 9007, St.Gallen, Switzerland.
BMC Dermatol. 2016 May 26;16(1):5. doi: 10.1186/s12895-016-0042-5.
Skin side effects during interferon-alpha and ribavirin treatment are common, but autoimmune dermatosis triggered by interferon-alpha is rare. We describe a case of erythrodermia from exacerbated psoriasis during the treatment of acute hepatitis C with pegylated-interferon-alpha and ribavirin. The incidence of psoriasis in this circumstance is unknown and only 36 cases are described in the literature, of which only one describes an erythrodermic psoriasis flare.
A 50-years old healthy white man presented with the complaints of headache, muscle pain, appetite loss, yellow skin complexion and fatigue. The laboratory results showed elevated liver enzymes above 50 times the upper limit of normal and a positive antibody test and RNA for hepatitis C. A screening test 6 months earlier was negative and therefore the diagnosis of an acute hepatitis C infection was most likely. In the absence of spontaneous clearance of the virus a therapy with pegylated- interferon-α and ribavirin was initiated. After 3 weeks the patient developed red scaly papular skin lesions that evolved despite treatment with prednisone to a severe erythrodermia. A skin biopsy showed typical signs for psoriasis vulgaris. Treatment with steroids was intensified and the hepatitis C therapy stopped. The patient achieved sustained virological response for hepatitis C, but psoriatic lesions were still present 6 months after treatment.
Although autoimmune skin reactions under pegylated-interferon-α and ribavirin treatment are rare it is important to recognise them early to start an adequate treatment to guarantee hepatitis C treatment continuation.
干扰素-α和利巴韦林治疗期间的皮肤副作用很常见,但由干扰素-α引发的自身免疫性皮肤病却很罕见。我们描述了一例在聚乙二醇化干扰素-α和利巴韦林治疗急性丙型肝炎期间,银屑病加重导致红皮病的病例。这种情况下银屑病的发病率尚不清楚,文献中仅描述了36例,其中只有一例描述了红皮病型银屑病发作。
一名50岁健康白人男性,主诉头痛、肌肉疼痛、食欲减退、皮肤发黄和疲劳。实验室检查结果显示肝酶升高超过正常上限50倍,丙型肝炎抗体检测和RNA呈阳性。6个月前的筛查试验为阴性,因此最有可能诊断为急性丙型肝炎感染。由于病毒未自发清除,开始使用聚乙二醇化干扰素-α和利巴韦林治疗。3周后,患者出现红色鳞屑丘疹性皮肤病变,尽管使用泼尼松治疗,仍发展为严重的红皮病。皮肤活检显示寻常型银屑病的典型体征。加强了类固醇治疗并停止了丙型肝炎治疗。患者实现了丙型肝炎的持续病毒学应答,但治疗6个月后银屑病病变仍然存在。
虽然聚乙二醇化干扰素-α和利巴韦林治疗下的自身免疫性皮肤反应很少见,但早期识别它们很重要,以便开始适当的治疗,保证丙型肝炎治疗的持续进行。