Pops M A
Calif Med. 1966 Sep;105(3):201-7.
In the past 10 years with the development of improved methods, particularly radioisotope techniques, it has been demonstrated that a number of patients with gastrointestinal disease and depletion of plasma proteins become hypoproteinemic because of actual leakage of albumin and other plasma proteins into the lumen of the gastrointestinal tract. The site of protein leakage is variable depending on the underlying pathological state but the loss of protein-containing lymph through the gastrointestinal lymphatic channels seems to be the major mechanism for hypoproteinemia.It has become apparent that there exists a normal mechanism for secretion of plasma proteins into the gastrointestinal tract as part of the overall metabolism of the plasma proteins. When the process is exaggerated so that resynthesis of plasma protein cannot keep pace with its degradation, sometimes severe hypoproteinemia is the result. Such a pathological process has now been described in approximately 40 disease states. A review of all the techniques which can demonstrate gastroenteric protein loss reveals that there are no widely available quantitative tests but that accurate quantitation is not necessary for the diagnosis of protein losing gastroenteropathy.
在过去10年里,随着改进方法的发展,尤其是放射性同位素技术的发展,已证实许多患有胃肠疾病且血浆蛋白减少的患者会因白蛋白和其他血浆蛋白实际漏入胃肠道管腔而出现低蛋白血症。蛋白质渗漏的部位因潜在病理状态而异,但含蛋白质的淋巴液通过胃肠淋巴通道流失似乎是低蛋白血症的主要机制。很明显,作为血浆蛋白整体代谢的一部分,存在将血浆蛋白分泌到胃肠道的正常机制。当这个过程被夸大,以至于血浆蛋白的再合成跟不上其降解速度时,有时就会导致严重的低蛋白血症。现在已在大约40种疾病状态中描述了这样一种病理过程。对所有能够证明胃肠蛋白丢失的技术进行综述后发现,目前尚无广泛可用的定量检测方法,但准确的定量检测对于蛋白丢失性胃肠病的诊断并非必要。