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萘普生导致的肝损伤。

Naproxen-induced liver injury.

机构信息

Department of Pathology and Laboratory Medicine, Henry Ford Hospital, 2799 West Grand Blvd., Detroit, MI 48202, USA.

出版信息

Hepatobiliary Pancreat Dis Int. 2011 Oct;10(5):552-6. doi: 10.1016/s1499-3872(11)60093-3.

Abstract

BACKGROUND

Nonsteroidal anti-inflammatory drugs (NSAIDs) have been reported to induce liver injury. Patterns of the injury usually range from mild elevations of liver enzymes to sometimes severe fulminant hepatic failure. Likewise, naproxen is a propionic acid derivative NSAID that was introduced in 1980 and has been available as an over-the-counter medication since 1994, but has rarely been reported to cause liver injury.

METHODS

We treated a 30-year-old woman with jaundice and intractable pruritus that developed shortly after taking naproxen. We reviewed the medical history and liver histopathology of the patient as well as all previously published case reports of naproxen-associated liver toxicity in the English language literature.

RESULTS

The liver biochemical profile of the patient revealed a mixed cholestasis and hepatitis pattern. Consecutive liver biopsies demonstrated focal lobular inflammation, hepatocyte drop-out, and a progressive loss of the small interlobular bile ducts (ductopenia). The biopsy performed two years after onset of the disease showed partial recovery of a small number of bile ducts; however, 10 years passed before the biochemical profile returned to near normal.

CONCLUSIONS

Naproxen-associated liver toxicity remains a rare entity, but should be considered in any patient presenting with cholestasis shortly after its use. Liver injury is most commonly seen in a mixed pattern characterized by cholestasis and hepatitis. The resulting liver damage may take years to resolve.

摘要

背景

非甾体抗炎药(NSAIDs)已被报道可导致肝损伤。损伤的模式通常从肝酶的轻度升高到有时严重的暴发性肝衰竭不等。同样,萘普生是一种丙酸衍生物 NSAID,于 1980 年推出,自 1994 年以来已作为非处方药供应,但很少有报道称其会导致肝损伤。

方法

我们治疗了一位 30 岁的女性,她在服用萘普生后不久出现黄疸和难治性瘙痒。我们回顾了患者的病史和肝组织病理学以及英语文献中所有先前发表的萘普生相关肝毒性病例报告。

结果

患者的肝功能生化谱显示混合性胆汁淤积和肝炎模式。连续的肝活检显示局灶性小叶炎症、肝细胞脱落和小肝内胆管(胆管减少)进行性丧失。发病两年后进行的活检显示少数胆管有部分恢复;然而,在生化谱恢复接近正常之前,又过了 10 年。

结论

萘普生相关的肝毒性仍然是一种罕见的实体,但应在任何患者在使用后不久出现胆汁淤积时考虑。肝损伤最常见于混合模式,表现为胆汁淤积和肝炎。由此产生的肝损伤可能需要数年才能解决。

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