Ades C J, Strutton G M, Walker N I, Furnival C M, Whiting G
Department of Pathology, Royal Brisbane Hospital, Australia.
J Clin Gastroenterol. 1989 Feb;11(1):85-7. doi: 10.1097/00004836-198902000-00022.
Fatal spontaneous rupture of the liver is described in a 46-year-old women with hepatic amyloidosis diagnosed premortem by liver biopsy. An autopsy revealed systemic amyloidosis, with no evidence of an underlying chronic inflammatory condition, infection, or immunocyte dyscrasia. By computerized search, this is only the third reported case of spontaneous rupture of the liver complicating amyloidosis.
一名46岁女性因肝活检在生前被诊断为肝淀粉样变性,出现致命性肝自发性破裂。尸检显示全身性淀粉样变性,无潜在慢性炎症性疾病、感染或免疫细胞异常的证据。通过计算机检索,这是第三例有报道的肝淀粉样变性并发自发性破裂的病例。