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.
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