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动脉性肝发育不良中的胆小管形态测量学

Bile canalicular morphometry in arteriohepatic dysplasia.

作者信息

Witzleben C L, Finegold M, Piccoli D A, Treem W R

机构信息

Department of Anatomic Pathology, Children's Hospital of Philadelphia, Pennsylvania 19104.

出版信息

Hepatology. 1987 Nov-Dec;7(6):1262-6. doi: 10.1002/hep.1840070614.

Abstract

The diagnosis of arteriohepatic dysplasia may be difficult, particularly in very young patients with no family history, and the pathogenesis of the disorder remains obscure. It has been reported that the typical ultrastructural changes of cholestasis are scant in this condition and proposed that there is a failure of the hepatocytes to secrete bile into the canaliculi. In an attempt to expand on these observations and to test the value of ultrastructure as a differential diagnostic test for this condition, we chose two parameters felt to be associated with cholestasis that could be reliably and relatively simply determined by ultrastructural morphometry: canalicular dilatation and loss of canalicular microvilli. The values for these parameters were compared in arteriohepatic dysplasia with those in other infantile cholestatic conditions and with those in noncholestatic controls. The results of these morphometric studies corroborated the previous observation that canalicular dilatation in arteriohepatic dysplasia is minimal. There was, however, only a marginal difference in canalicular area between patients with arteriohepatic dysplasia and those with extrahepatic biliary atresia. There was significant overlap of values for canalicular area among all groups. Surprisingly, the studies showed no real loss of canalicular microvilli in any of the cholestatic conditions. The findings suggest that, at least for these two parameters, caution should be exercised in using qualitative electron microscopic evaluation as a diagnostic test for arteriohepatic dysplasia.

摘要

动脉肝发育不良的诊断可能很困难,尤其是在没有家族史的非常年幼的患者中,而且这种疾病的发病机制仍不清楚。据报道,在这种情况下胆汁淤积的典型超微结构变化很少,有人提出肝细胞无法将胆汁分泌到胆小管中。为了进一步阐述这些观察结果,并测试超微结构作为这种疾病鉴别诊断试验的价值,我们选择了两个被认为与胆汁淤积相关的参数,这些参数可以通过超微结构形态计量学可靠且相对简单地确定:胆小管扩张和胆小管微绒毛丧失。将动脉肝发育不良患者的这些参数值与其他婴儿胆汁淤积性疾病患者以及非胆汁淤积性对照者的参数值进行比较。这些形态计量学研究的结果证实了先前的观察结果,即动脉肝发育不良中的胆小管扩张最小。然而,动脉肝发育不良患者与肝外胆道闭锁患者之间的胆小管面积仅存在微小差异。所有组之间胆小管面积值存在显著重叠。令人惊讶的是,研究表明在任何胆汁淤积性疾病中都没有真正的胆小管微绒毛丧失。这些发现表明,至少对于这两个参数,在将定性电子显微镜评估用作动脉肝发育不良的诊断试验时应谨慎。

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