Ouellette G S, Slitzky B E, Gates J A, Lagarde S, West A B
Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06510-8070.
J Clin Gastroenterol. 1991 Apr;13(2):205-10. doi: 10.1097/00004836-199104000-00018.
We describe the clinical features, liver histology, and ultrastructure in reversible diclofenac-induced hepatitis and review previous reports of this entity. Although rarely reported, diclofenac hepatitis may be severe, and even fatal. Symptoms, which develop from 1 week to 11 months after starting the drug, include jaundice, pruritus, fever, abdominal pain, nausea, vomiting, and rash. Bilirubin and alkaline phosphatase are mildly elevated, transaminases often markedly so. The nature of the idiosyncratic injury appears variable, some cases having features of a hypersensitivity reaction, most being more suggestive of a toxic metabolic effect. Light microscopy shows a nonspecific hepatitis with portal and lobular activity, and focal hepatocellular injury that may progress to zonal or massive necrosis. The ultrastructural features in our case are typical of drug or toxin injury. This may be of value in distinguishing this entity from other forms of hepatitis, which is important in view of the frequent reversibility of this potentially lethal form of injury.
我们描述了可逆性双氯芬酸诱导的肝炎的临床特征、肝脏组织学和超微结构,并回顾了此前关于该病症的报告。双氯芬酸肝炎虽鲜有报道,但可能很严重,甚至致命。症状在开始用药后1周~11个月出现,包括黄疸、瘙痒、发热、腹痛、恶心、呕吐和皮疹。胆红素和碱性磷酸酶轻度升高,转氨酶通常显著升高。特异质性损伤的性质似乎各不相同,一些病例具有超敏反应的特征,大多数更提示为毒性代谢作用。光镜检查显示为非特异性肝炎,伴有门脉区和小叶区活动,以及局灶性肝细胞损伤,后者可能进展为带状或大块坏死。我们病例的超微结构特征是典型的药物或毒素损伤。这可能有助于将该病症与其他形式的肝炎区分开来,鉴于这种潜在致命性损伤形式常常具有可逆性,这一点很重要。