先天性肝内胆管囊性扩张(卡罗里氏病)。

Radiologia clinica Pub Date : 1978-01-01
G A In der Maur, B J Zuidema, S A Duursma, W F Blom
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引用次数: 0

摘要

本文报告1例卡罗里氏病(肝内胆管节段性扩张)的临床特点。这种情况不同于其他胆管囊性扩张,因为它只累及肝内胆管。其发病机制尚不清楚。怀疑胆管壁的胚胎发育障碍是通过生理上周期性的压力增加引起囊肿的。诊断是在胆囊切除术期间或之后通过t型引流管进行的胆管造影。当怀疑卡罗里氏病时,超声检查是一种有价值的诊断辅助手段。
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Congenital cystic dilatation of the intrahepatic bile ducts (Caroli's disease).

With reference to a patient with Caroli's disease (segmentally dilatated intrahepatic bile ducts), the clinical features of this rare but serious disease are described. The condition differs from other cystic dilatations of the bile ducts in that only the intrahepatic bile ducts are involved. Its pathogenesis is obscure. It is suspected that an embryonic developmental disorder in the wall of the bile ducts causes cysts via physiological periodical increases of pressure. The diagnosis is made accidentally by cholangiography via the T-drain during or after cholecystectomy. When Caroli's disease is suspected, echography can be a valuable diagnostic aid.

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