Francis J L, Armstrong D J
J Clin Pathol. 1982 Jun;35(6):667-72. doi: 10.1136/jcp.35.6.667.
Using a new and sensitive screening method, dysfibrinogenaemia (DF) was detected in 76% of patients with cirrhosis, 78% with chronic active liver disease and 86% with acute liver failure. The incidence was much lower in obstructive jaundice (8%) and miscellaneous liver disorders (4%). It is concluded that the fibrin monomer polymerisation (FMP) ratio test is a simple and sensitive test for the detection of DF, and is useful in the differential diagnosis of hepatocellular and obstructive jaundice. Hyperfibrinogenaemia, particularly in patients with obstructive jaundice, may explain the high incidence of abnormal thrombin and Reptilase clotting times despite normal FMP ratios. Dysfibrinogenaemia dose not appear to be related to the degree of liver function impairment, but may be associated with regeneration of hepatic tissue.
采用一种新的敏感筛查方法,在76%的肝硬化患者、78%的慢性活动性肝病患者和86%的急性肝衰竭患者中检测到异常纤维蛋白原血症(DF)。在梗阻性黄疸患者中发病率低得多(8%),在其他肝病中为4%。结论是,纤维蛋白单体聚合(FMP)比率试验是检测DF的一种简单而敏感的试验,对肝细胞性黄疸和梗阻性黄疸的鉴别诊断有用。纤维蛋白原血症过高,尤其是在梗阻性黄疸患者中,可能解释了尽管FMP比率正常,但凝血酶和爬虫酶凝血时间异常的高发生率。异常纤维蛋白原血症似乎与肝功能损害程度无关,但可能与肝组织再生有关。