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部分脾栓塞治疗儿童遗传性贫血的术后反应、并发症及其处理 被引量:16

Partial Splenic Embolization in the Treatment of Hereditary Anemia in Children : Post-Embolization Reactions and Complications
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摘要 对106例地中海贫血和遗传性球形红细胞增多症患儿行部分性脾栓塞(PSE)治疗。栓塞范围在50%~85%。其术后反应包括发热(95%)、上腹痛(95%)和恶心呕吐(55%),一般在3~10天自行消失。持续性高热往往提示大面积的脾坏死或液化坏死。并发症的发生率为17.9%,包括脾液化坏死(12例,占60%),一过性高血压(3例,16%),肺炎(2例,11%),急性胰腺炎(1例,6%)和机械性肠梗阻(1例,6%)。其中较大的液化坏死采用经皮穿刺引流治疗。所有并发症均痊愈,本组无死亡及严重后遗症病例。作者认为PSE对儿童遗传性贫血是安全的疗法。 Partial splenic embolization (PSE) was used to treat hereditary anemia in 106 chil-dren, including thalassemia major and hereditary spherocytosis, The embolization of spleen ranged from 50% to 85% , The post-pSE reactions included fever (95%), upper abdominal pain (95%)and nausea (55%). Generally, the symptoms disapeared in 3~10 days. Persistent high fever probably is a forewarning of a large area of splenic necrosis or liquefied necrosis, Incidence of the complications was 17.9% , including splenic necrosis (12 cases, 60% ), transient hypertension (3 cases, 16% )pneumonia(2 cases,11% ), acute pancreatitis ( 1 case, 6% ), and mechanical intesinal obstruction(1 case, 6% ). Liquefied necrosis was treated by percutaneous drainage. All the complications were cured without fatality or severe sequalae. It is believed that PSE is a safe therapy for children with hereditary anemia.
作者 陈勇 李彦豪
出处 《中华放射学杂志》 CAS CSCD 北大核心 1995年第8期534-537,共4页 Chinese Journal of Radiology
关键词 地中海贫血 球形红细胞增多 部分性脾栓塞 栓塞 Embolization, therapeutic Thalassemia Spleen Children
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参考文献4

  • 1杨彤翰,第三军医大学学报,1989年,11卷,380页
  • 2李红旗,中国医学影像技术杂志,1988年,4卷,36页
  • 3李楚杰,病理生理学报,1985年,1卷,58页
  • 4孙大裕,介入放射学,1985年

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