Arnold G L, Kaplan M M
Am J Gastroenterol. 1979 Feb;71(2):213-6.
Peliosis hepatis is a rare hepatic disorder mainly diagnosed at surgery or autopsy. Clinical outcome is thus frequently poor. We report a patient in whom the diagnosis was established by percutaneous needly biopsy. Withdrawal of the steroid medication was followed by a prompt clinical improvement. Although histologic proof of regression is not available, this experience suggests a more favorable prognosis than previously thought possible.
肝紫癜病是一种罕见的肝脏疾病,主要在手术或尸检时被诊断出来。因此,临床预后往往很差。我们报告了一名通过经皮穿刺活检确诊的患者。停用类固醇药物后,患者的临床症状迅速改善。尽管目前尚无组织学证据证明病情已消退,但这一经验表明,其预后可能比之前认为的更为乐观。