Foged E, Bjerring P, Kragballe K, Søgaard H, Zachariae H
J Am Acad Dermatol. 1984 Oct;11(4 Pt 1):580-3. doi: 10.1016/s0190-9622(84)70209-x.
Histologic changes in the liver were evaluated in thirty-two patients with different dyskeratotic dermatoses treated with etretinate (Tigason) during an average of 24.9 months. Fatty infiltration, nuclear variability, periportal inflammation, focal necrosis, fibrosis, and cholestasis were estimated. The usual dose was 50-75 mg/day, with reduction according to efficacy and side effects. No statistically significant differences were found between a control group of thirty-five liver biopsies from psoriasis patients who had not received systemic therapy and biopsies from the patients treated with etretinate. Among the thirty-two etretinate-treated patients, six had two serial biopsies, and eight had pretreatment biopsies. No significant changes appeared during therapy.
在平均24.9个月的时间里,对32例接受依曲替酯(银屑灵)治疗的不同角化异常性皮肤病患者的肝脏组织学变化进行了评估。评估了脂肪浸润、核异型性、汇管区炎症、局灶性坏死、纤维化和胆汁淤积情况。通常剂量为50 - 75毫克/天,并根据疗效和副作用进行减量。在未接受全身治疗的银屑病患者的35份肝脏活检标本组成的对照组与接受依曲替酯治疗患者的活检标本之间,未发现统计学上的显著差异。在32例接受依曲替酯治疗的患者中,6例进行了两次连续活检,8例进行了治疗前活检。治疗期间未出现显著变化。