本文關鍵詞： 先天性疾病 門靜脈畸形 肝外門體靜脈分流　出處：《介入放射學雜志》2017年10期 　論文類型：期刊論文

【摘要】：正臨床資料病例1:男,10歲。因"皮膚青紫半年余"入院。查體:SPO288%(未吸氧),杵狀指。心肺聽診無異常。實驗室檢查無明顯異常。心臟彩超示第一肝門區(qū)異常靜脈團(先天性門體靜脈分流?)。CT增強示食管、胃底、腸系膜上、下靜脈經共同干匯入脾門區(qū)扭曲、擴張血管團,再下行匯入左腎靜脈(圖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).
【作者單位】： 蘇州大學附屬兒童醫(yī)院影像科;
【分類號】：R445.2;R725.7;R816.92
【正文快照】： 臨床資料病例1:男,10歲。因“皮膚青紫半年余”入院。查體:SPO288%(未吸氧),杵狀指。心肺聽診無異常。實驗室檢查無明顯異常。心臟彩超示第一肝門區(qū)異常靜脈團(先天性門體靜脈分流?)。CT增強示食管、胃底、腸系膜上、下靜脈經共同干匯入脾門區(qū)扭曲、擴張血管團,再下行匯入左腎，

本文編號：1453067