Nyfors A, Poulsen H
Am J Surg Pathol. 1977 Sep;1(3):235-43. doi: 10.1097/00000478-197709000-00005.
Serial liver biopsies before and after Methotrexate therapy were performed in each of eight patients with severe, recalcitrant psoriasis treated for years with Methotrexate in a single, weekly, oral dose not exceeding 25 mg per dose. A total of 31 liver biopsies was studied. The study revealed liver damage commencing with small foci of piecemeal necrosis, followed by the destruction of the limiting plate and the occurrence of stellate periportal fibrosis. Eventually, partial and then whole fibrous septa developed between portal tracts and between portal tracts and central veins, with resultant distortions of the lobular architecture. In two patients with an admitted daily alcoholic intake, additional findings were seen, including alcoholic hepatitis, centrilobular fibrosis and development of partial and whole fibrous septa between the central vein area, and portal tracts adding to the number of septa running between the portal tracts and central veins which split up the lobules. The following conclusions seem probable: 1) Methotrexate therapy in psoriatics may cause development of fibrosis or cirrhosis; 2) the morphological changes during this development follow a consistent pattern; and 3) the pathogenesis of the development of fibrosis and cirrhosis is mixed in some cases, being dependent on both alcoholic and Methotrexate intake.
对8例严重顽固性银屑病患者进行了甲氨蝶呤治疗前后的系列肝脏活检。这些患者多年来一直接受甲氨蝶呤单药治疗,每周口服一次,每次剂量不超过25mg。共研究了31次肝脏活检。研究发现肝脏损伤始于小灶性碎片状坏死,随后是界板破坏和星芒状汇管区周围纤维化的出现。最终,汇管区之间以及汇管区与中央静脉之间出现部分和完全的纤维间隔,导致小叶结构扭曲。在2例承认有每日酒精摄入量的患者中,还发现了其他病变,包括酒精性肝炎、中央小叶纤维化以及中央静脉区域与汇管区之间出现部分和完全的纤维间隔,增加了分隔小叶的汇管区与中央静脉之间的间隔数量。以下结论似乎是可能的:1)银屑病患者接受甲氨蝶呤治疗可能会导致纤维化或肝硬化的发展;2)这种发展过程中的形态学变化遵循一致的模式;3)在某些情况下,纤维化和肝硬化发展的发病机制是混合性的,取决于酒精摄入和甲氨蝶呤的服用情况。