glafenine相关的肝损伤。38例病例分析及文献复习。

Liver Pub Date : 1986-04-01
B H Stricker, A P Blok, F B Bronkhorst
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引用次数: 0

摘要

Glafenine伴肝损伤38例。因果关系是根据与药物使用、疗程和排除其他原因的时间关系来评估的。在27个案例中,因果关系被认为是可能的。“可能”(12例)或“可能”(15例),而在11例中,要么不太可能,要么无法分类。在“可能”组和“可能”组中,60-70%的人都是女性。两组中四分之三的病例都有黄疸。嗜酸性粒细胞增多症在“可能”病例组中更为常见,这一组的病死率最高(42%)。起病时间从2天到8个月不等,但大多数病例出现在开始治疗后2周到4个月之间。22例组织学表现为主要的肝细胞型,从点状全小叶坏死、小叶中心和(亚)大量坏死(急性型)到纤维化和肝硬化(慢性型)不等。glafenine的化学结构和临床病理模式与cinchophen相似。发病率尚不清楚。代谢特性或免疫过敏机制似乎是负责任的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glafenine-associated hepatic injury. Analysis of 38 cases and review of the literature.

Glafenine was associated with hepatic injury in 38 cases. The causal relationship was assessed on the basis of the temporal relationship with drug use, course and exclusion of other causes. In 27 cases a causal relationship was considered likely, i.e. 'probable' (12 cases) or 'possible' (15 cases), whereas in 11 cases it was either unlikely or unclassifiable. In both the 'probable' and 'possible' groups 60-70% of individuals were women. Jaundice was present in three-quarters of cases in both groups. Eosinophilia was more frequent in the group of 'probable' cases, and this group had the highest case-fatality rate (42%). Onset varied from 2 days (after a rechallenge) to 8 months, but most cases appeared between 2 weeks and 4 months after starting therapy. Histology in 22 cases showed a predominantly hepatocellular pattern, varying from spotty panlobular necrosis, centrilobular and (sub)massive necrosis (acute pattern) to fibrosis and cirrhosis (chronic pattern). The chemical structure of glafenine and the clinicopathological pattern it induces resemble that of cinchophen. The incidence is unknown. Either metabolic idiosyncrasy or an immunoallergic mechanism seems to be responsible.

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