Wood L J, Mundo F, Searle J, Powell L W
Aust N Z J Med. 1985 Aug;15(4):397-401. doi: 10.1111/j.1445-5994.1985.tb02758.x.
Sulindac (Clinoril), an anti-inflammatory drug increasingly used in Australia for the treatment of rheumatological conditions, is unpredictably associated with a cholestatic hepatitis. We present three cases of sulindac hepatitis. The first case exemplifies acute sulindac hepatitis, the second, continuously exposed to sulindac for 18 months, had chronic sulindac hepatotoxicity, and in the third case, the long-term histological outcome after cessation of sulindac is described. The clinical, biochemical, and histopathological characteristics are those of a cholestatic hepatitis which resolves on withdrawal of the drug. We report marked anisonucleosis with cytoplasmic invaginations into the nucleus and binuclearity of hepatocytes as additional histological features of sulindac hepatitis. There is no evidence that sulindac hepatitis progresses to irreversible structural liver damage, although nuclear changes may persist for up to two months after cessation of the drug. The clinical and biochemical features of all reported cases of sulindac hepatitis are summarised.
舒林酸(奇诺力)是一种抗炎药物,在澳大利亚越来越多地用于治疗风湿性疾病,但它与胆汁淤积性肝炎的关联不可预测。我们报告三例舒林酸肝炎病例。第一例为急性舒林酸肝炎,第二例连续服用舒林酸18个月,出现慢性舒林酸肝毒性,第三例描述了停用舒林酸后的长期组织学转归。临床、生化和组织病理学特征均符合胆汁淤积性肝炎,停药后可缓解。我们报告舒林酸肝炎的额外组织学特征为明显的核仁大小不均、细胞质向细胞核内凹陷以及肝细胞双核化。尽管停药后核变化可能持续长达两个月,但尚无证据表明舒林酸肝炎会进展为不可逆的肝脏结构损伤。本文总结了所有已报道的舒林酸肝炎病例的临床和生化特征。