Rare Cause of Obstructive Jaundice in a Young Female

D. P, Nair Sp, J. P., T. R, J. S., Jain Ss, Sonthalia N Rathi PM, U. S.
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引用次数: 1

Abstract

Introduction: Congenital common bile duct (CBD) webs are extremely rare abnormalities of the extra hepatic ducts with approximately 10 cases reported in the literature. The age at presentation and the clinical symptomatology of these anomalies depend on the grade of the biliary obstruction. These webs usually exhibit early in life as obstructive jaundice, dilation of the proximal biliary tree or even spontaneous perforation of the extra hepatic duct. Some of these congenital webs are partially developed and remain asymptomatic until adulthood. Case Report: 28 year female patient presented with cholestatic pattern jaundice for 2 months. On evaluation found to have dilated CBD with IHBRD on USG. On further imaging studies, CT revealed horizontal web like projection from distal CBD suggestive of web with similar findings on MRCP. ERCP showed horizontal filling defect on cholangiogram with dilated CBD. Endoscopic Ultrasound examination revealed horizontal hyper echoic structure at distal CBD with proximally dilated CBD and IHBRD. Dilatation was performed using Soehendra Biliary Dilation Catheter with significant improvement in her symptomatology. Conclusion: Our case remains the first of its kind in which EUS characterisation of CBD web is described. Though rare congenital anomalies remain an important cause of young patients presenting with obstructive jaundice. Treatment for such cases remains Endoscopic dilatation or surgical by-pass in which endoscopic treatment fails. Keywords: Common bile duct web; Obstructive jaundice; Soehendra Biliary Dilation Catheter; Endoscopic Ultrasound. Abbreviations: HB-Haemoglobin; TLC-Total Leucocyte Count; AST-Aspartate Transaminase; ALT-Alanine Transaminase; ALPAlkaline Phosphatase; USG- Ultrasonography; IHBRD- Intra-hepatic biliary radicle, CBD- Common bile duct; GB- Gall bladder; MRCPMagnetic Resonance Cholangio-Pancreatography
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一位年轻女性梗阻性黄疸的罕见病因
简介:先天性胆总管网是一种极为罕见的肝外管异常,文献报道约有10例。出现的年龄和这些异常的临床症状取决于胆道阻塞的程度。这些网通常在生命早期表现为梗阻性黄疸,近端胆道扩张,甚至自发肝外管穿孔。这些先天性蜘蛛网有些是部分发育的,直到成年后才会出现症状。病例报告:女性,28岁,以胆汁淤积型黄疸就诊2个月。经评估发现在USG上使用IHBRD扩展CBD。在进一步的影像学研究中,CT显示CBD远端水平网状投影,提示网状,MRCP类似。ERCP显示胆管造影水平充盈缺损,CBD扩张。超声内镜检查显示CBD远端水平高回声结构,近端扩张CBD和IHBRD。使用Soehendra胆道扩张导管进行扩张,症状明显改善。结论:我们的病例仍然是第一个此类的EUS特征的CBD网被描述。尽管罕见的先天性异常仍然是年轻患者表现为阻塞性黄疸的重要原因。这种情况的治疗仍然是内镜扩张或手术旁路,其中内镜治疗失败。关键词:胆总管网;阻塞性黄疸;Soehendra胆道扩张导管;内窥镜超声检查。缩写:HB-Haemoglobin;tlc -总白细胞计数;AST-Aspartate转氨酶;alt谷丙转氨酶;ALPAlkaline磷酸酶;USG—超声;IHBRD-肝内胆根,CBD-胆总管;GB—胆囊;磁共振胆道胰腺造影
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