胆总管囊肿的胎儿磁共振成像

D. A. Wirasasmita, Gatot Abdurrazak, A. Yani
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引用次数: 0

摘要

胆总管囊肿是一种罕见的先天性异常,以肝内或肝外胆管扩张为特征。由于高分辨率超声(US)和超快序列磁共振成像(MRI)能更好地描绘囊肿和邻近结构,产前诊断越来越多。考虑到胎儿MRI报告的附加价值仍然很少证实CC病例,因此我们报告I型CC,之前从US结果诊断为胆囊胆闭锁(CBA)。产后MRI和组织病理学证实了这一点。
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Fetal Magnetic Resonance Imaging of Choledochal Cyst
Choledochal cysts (CCs) are rare congenital anomaly with characterized dilatation of intraor extrahepatic biliary duct or both. Prenatal diagnosis is increasing due to high resolution of ultrasound (US) and ultrafast sequences of magnetic resonance imaging (MRI) showing better delineation of the cyst to the adjacent structure. Considering the additional value of the fetal MRI report is still infrequent to confirm the CC case, we therefore report the type I of CC, which was previously diagnosed as a cystic biliary atresia (CBA) from US result. Postnatal MRI and histopathology prove it.
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