先天性肝外门体分流2例

发布时间：2018-01-22 00:41

  本文关键词： 先天性疾病 门静脉畸形 肝外门体静脉分流　出处：《介入放射学杂志》2017年10期 　论文类型：期刊论文

【摘要】：正临床资料病例1:男,10岁。因"皮肤青紫半年余"入院。查体:SPO288%(未吸氧),杵状指。心肺听诊无异常。实验室检查无明显异常。心脏彩超示第一肝门区异常静脉团(先天性门体静脉分流?)。CT增强示食管、胃底、肠系膜上、下静脉经共同干汇入脾门区扭曲、扩张血管团,再下行汇入左肾静脉(图1(1))。肝
[Abstract]:Case 1: male was 10 years old. He was admitted to hospital because of "skin blue and purple for more than half a year". Clubbing finger. No abnormal cardiac and pulmonary auscultation. No obvious abnormality in laboratory examination. Color Doppler echocardiography showed abnormal venous mass in the first hepatic portal area (congenital portosystemic shunt? Ct enhancement shows the esophagus, stomach fundus, superior mesenteric vein and inferior vein confluent through the common trunk into the portal area of the spleen, dilating the vascular mass, and then descending into the left renal vein (fig. 1).
【作者单位】： 苏州大学附属儿童医院影像科;
【分类号】：R445.2;R725.7;R816.92
【正文快照】： 临床资料病例1:男,10岁。因“皮肤青紫半年余”入院。查体:SPO288%(未吸氧),杵状指。心肺听诊无异常。实验室检查无明显异常。心脏彩超示第一肝门区异常静脉团(先天性门体静脉分流?)。CT增强示食管、胃底、肠系膜上、下静脉经共同干汇入脾门区扭曲、扩张血管团,再下行汇入左肾，

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