Cystic Biliary Atresia: A Delayed Diagnosis of Obstructive Jaundice

Aishath Azna Ali, F. Hayati, N. Azizan, Che Ismail Che Noh, Marjmin Osman
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Abstract

Cystic biliary atresia is an uncommon variant of biliary atresia. It is the most usual cause of neonatal jaundice which requires surgical intervention and liver transplantation in children. Herein, we present a case of a 2-month-old baby with persistent obstructive jaundice, who was not properly investigated prior to this. After the diagnosis has been established, we proceeded with the Kasai-type portoenterostomy. Even slightly delayed, the patient recovered well postoperatively and subsequently jaundice resolved.
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胆囊胆道闭锁:梗阻性黄疸的延迟诊断
胆囊性胆道闭锁是一种少见的胆道闭锁。它是新生儿黄疸最常见的原因,需要手术干预和儿童肝移植。在这里,我们提出了一个2个月大的婴儿持续梗阻性黄疸的情况下,谁没有适当的调查之前,这。确诊后,我们进行了kasai型门静脉肠造口术。即使稍微延迟,患者术后恢复良好,随后黄疸消退。
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