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首页> 外文期刊>Journal of Clinical Imaging Science >Giant Choledochal Cyst Mimicking Massive Gallbladder Hydrops in an Adult Patient: Multi Detector Computed Tomography and Magnetic Resonance Imaging Findings Correlated to Gross and Histopathological Findings
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Giant Choledochal Cyst Mimicking Massive Gallbladder Hydrops in an Adult Patient: Multi Detector Computed Tomography and Magnetic Resonance Imaging Findings Correlated to Gross and Histopathological Findings

机译:成年患者模仿胆囊积水的巨大胆总管囊肿:与总体和组织病理学发现相关的多探测器计算机断层扫描和磁共振成像发现

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Choledochal cysts are uncommon congenital anomalies of the biliary tree, commonly presenting in infancy, generally in the 1st year of life. Presentation in adult life is less common, accounting for 20% of cases. A 19-year-old female patient presented to the Emergency Department with severe abdominal distension, a palpable abdominal mass, mild jaundice and low grade fever. Ultrasound, computed tomography (CT) and magnetic resonance imaging of the abdomen showed a massive septated cystic lesion filling the entire abdomen with a significant mass effect on surrounding structures. Origin of the lesion was unclear and diagnosis included a giant mesenteric or duplication cyst, massive gallbladder with hydrops, biliary cystadenoma and giant choledochal cyst, among others. Final diagnosis was a Type IA choledochal cyst with massive asymmetric cystic dilatation of the extra-hepatic segments of the left hepatic duct with asymmetric dilatation of the right hepatic duct. Patient had an uneventful recovery after resection of the entire extrahepatic cyst and Roux-en-Y hepaticojejunostomy at the level of the hilum. In this article, we correlate CT and MRI findings to gross and histopathological findings of this giant Todani's Type IA choledochal cyst.Keywords: Choledochal cysts, computed tomography, gallbladder hydrops, magnetic resonance cholangiopancreaticography
机译:胆总管囊肿是胆道树的罕见先天性异常,通常在婴儿期出现,通常发生在生命的第一年。成人生活中的表现较少见,占病例的20%。一名19岁的女性患者因严重的腹胀,明显的腹部肿块,轻度黄疸和低烧出现在急诊室。腹部的超声,计算机断层扫描(CT)和磁共振成像显示,巨大的分隔性囊性病变充满整个腹部,对周围结构有明显的质量效应。病变的起源尚不清楚,诊断包括巨大的肠系膜或重复性囊肿,巨大的胆囊积液,胆囊性膀胱腺瘤和巨大的胆总管囊肿。最终诊断为IA型胆总管囊肿,左肝管肝外段大量不对称囊性扩张,右肝管不对称扩张。切除整个肝外囊肿并在肺门水平行Roux-en-Y肝空肠吻合术后,患者恢复良好。在本文中,我们将CT和MRI表现与该巨大的Todani IA型胆总管囊肿的肉眼和组织病理学发现相关联。

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