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家族性低纤维蛋白原血症中的肝细胞纤维蛋白原储存

Hepatocellular fibrinogen storage in familial hypofibrinogenemia.

作者信息

Pfeifer U, Ormanns W, Klinge O

出版信息

Virchows Arch B Cell Pathol Incl Mol Pathol. 1981;36(2-3):247-55. doi: 10.1007/BF02912070.

Abstract

In the cytoplasm of hepatocytes of liver biopsy from a 30 year old man, there were proteinaceous inclusions which by use of the peroxidase-antiperoxidase method reacted strongly with antihuman-fibrinogen IgG, but gave a negative reaction with antihuman-alpha-1-antitrypsin IgG and with antihuman-albumin IgG. As shown in the electron microscope, these protein inclusions were composed of densely packed, irregularly arranged tubules of 40 nm diameter. Clinically, the patient and members of his family showed primary hypofibrinogenemia which on the basis of the morphological findings has to be interpreted as the consequence of a disturbance in the secretion of fibrinogen. Besides the well known alpha-1-antitrypsin deficiency, familial hypofibrinogenemia with hepatocellular fibrinogen storage appears to represent another example of a plasma deficiency due to failure of hepatic secretion.

摘要

在一名30岁男性肝脏活检的肝细胞胞质中,存在蛋白质性包涵体。运用过氧化物酶-抗过氧化物酶方法,这些包涵体与抗人纤维蛋白原IgG发生强烈反应,但与抗人α-1-抗胰蛋白酶IgG及抗人白蛋白IgG呈阴性反应。如电子显微镜所示,这些蛋白质包涵体由直径40nm、紧密堆积且排列不规则的小管组成。临床上,该患者及其家族成员表现为原发性低纤维蛋白原血症,基于形态学发现,这必须被解释为纤维蛋白原分泌紊乱的结果。除了众所周知的α-1-抗胰蛋白酶缺乏症外,伴有肝细胞纤维蛋白原储存的家族性低纤维蛋白原血症似乎代表了另一个因肝脏分泌功能衰竭导致的血浆缺乏症实例。

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