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甲氨蝶呤治疗银屑病患者的肝脏活检——重新评估

Liver biopsy in methotrexate-treated psoriatics-a re-evalution.

作者信息

Zachariae H, Grunnet E, Sogaard H

出版信息

Acta Derm Venereol. 1975;55(4):291-6.

PMID:52258
Abstract

Two-hundred and eighty-six liver biopsies were performed in 139 psoriatics on treatment or considered for treatment with methotrexate. In 56 psoriatics included in this study both pre- and post-methotrexate biopsies were performed, the average methotrexate dose being 936 mg. None of the data showed statistically significant differences between pre- and post-methotrexate biopsies, with the exception of an increase in fattly infiltration, found when comparing all pre-methotrexate biopsies with the total number of latest post-methotrexate samples. As expected, alcohol seemed to be significantly associated with liver fibrosis in pre-methotrexate biopsies. An patients, although potassium arsenite alone has not been proved to be the cause of liver damage among psoriatics included in this study. While only 1 of 22 psoriatics with a total normal biopsy had been on arsenite, 6 of 18 of the same group of psoriatics who had fibrosis had been on this drug earlier. Although no statistically significant differences related to fibrosis and cirrhosis could that in three cases liver cirrhosis did appear in a biopsy from a methotrexate-treated psoriatic who had signs of fibrosis of cirrhosis in a pre-methotrexate biopsy. This incidence is low in relation to the total number of patients treated. The relatively low incidence of cirrhosis found in the present study, as in earlier studies by our group is believed to be due to the use of an intermittent dosage schedule. The study showed that early fibrosis and cirrhosis seem to appear, with very minor abnormalities in laboratory results. This finding indicates the necessity of performing liver biopsies in the control of psoriatics on long-term methotrexate therapy. The difference between biopsies from psoriatics and liver biopsies from control patients may indicate that severity of disease may be a complicating factor in the pathogenesis of the liver damage.

摘要

对139例接受甲氨蝶呤治疗或考虑接受该治疗的银屑病患者进行了286次肝活检。本研究纳入的56例银屑病患者在甲氨蝶呤治疗前后均进行了活检,甲氨蝶呤平均剂量为936毫克。除了将所有甲氨蝶呤治疗前的活检与最新的甲氨蝶呤治疗后的样本总数进行比较时发现脂肪浸润增加外,没有数据显示甲氨蝶呤治疗前后的活检有统计学上的显著差异。正如预期的那样,在甲氨蝶呤治疗前的活检中,酒精似乎与肝纤维化显著相关。在本研究纳入的银屑病患者中,虽然单独使用亚砷酸钾尚未被证明是肝损伤的原因。在22例活检完全正常的银屑病患者中,只有1例曾使用过亚砷酸钾,而在同一组有纤维化的18例银屑病患者中,有6例曾较早使用过该药物。虽然与纤维化和肝硬化没有统计学上的显著差异,但在3例病例中,一名接受甲氨蝶呤治疗的银屑病患者在甲氨蝶呤治疗前的活检中有肝硬化纤维化迹象,而在活检中确实出现了肝硬化。相对于接受治疗的患者总数而言,这一发生率较低。本研究中发现的肝硬化发生率相对较低,正如我们小组早期的研究一样,被认为是由于采用了间歇给药方案。研究表明,早期纤维化和肝硬化似乎会出现,而实验室结果只有非常轻微的异常。这一发现表明,在对长期接受甲氨蝶呤治疗的银屑病患者进行监测时,有必要进行肝活检。银屑病患者的活检与对照患者的肝活检之间的差异可能表明,疾病的严重程度可能是肝损伤发病机制中的一个复杂因素。

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