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中毒性油综合征的临床生化演变及晚期肝脏病变

Clinico-biochemical evolution and late hepatic lesions in the toxic oil syndrome.

作者信息

Solis-Herruzo J A, Vidal J V, Colina F, Castellano G, Muñoz-Yagüe M T, Morillas J D

出版信息

Gastroenterology. 1987 Sep;93(3):558-68. doi: 10.1016/0016-5085(87)90919-x.

Abstract

The clinical and biochemical evolution of hepatic lesions in 124 patients with toxic oil syndrome from 1981 to 1986 has been reviewed. Most patients became asymptomatic during the early phase of the disease and abnormal liver function tests gradually normalized. In 1981, liver injury resembled drug-induced cholestatic hepatitis in 31 patients, and in 1 patient chronic destructive nonsuppurative cholangitis was evident. From 1982 to 1986 serial liver biopsies demonstrated toxic cholestatic hepatitis in 14 patients, chronic active hepatitis in 13, and nonalcoholic cirrhosis in 4. Nineteen patients showed lesions suggestive of alcoholic liver disease, but only 8 had a history of heavy alcohol intake. One patient developed biliary cirrhosis, another liver cell adenoma, and 8 nodular regenerative hyperplasia of the liver. We conclude that although liver injury had subsided in most patients, a significant number developed a variety of different liver diseases after follow-up for 5 yr.

摘要

回顾了1981年至1986年124例中毒性油综合征患者肝脏病变的临床和生化演变情况。大多数患者在疾病早期阶段无症状,肝功能检查异常逐渐恢复正常。1981年,31例患者的肝损伤类似药物性胆汁淤积性肝炎,1例患者表现为明显的慢性破坏性非化脓性胆管炎。1982年至1986年的系列肝活检显示,14例患者为中毒性胆汁淤积性肝炎,13例为慢性活动性肝炎,4例为非酒精性肝硬化。19例患者表现出提示酒精性肝病的病变,但只有8例有大量饮酒史。1例患者发展为胆汁性肝硬化,另1例为肝细胞腺瘤,8例为肝脏结节状再生性增生。我们得出结论,尽管大多数患者的肝损伤已消退,但随访5年后仍有相当数量的患者发展为各种不同的肝脏疾病。

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