ACRP  >> Vol. 1 No. 3 (August 2013)

    One Case Report of Hypereosinophilic Carditis Combined Cerebral Infarction in Child

  • 全文下载: PDF(189KB) HTML    PP.53-55   DOI: 10.12677/ACRP.2013.13014  
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蔺 萃,张永法:潍坊医学院附属益都中心医院儿内二科;

脑梗塞儿童嗜酸性粒细胞增多综合征Cerebral Infarction; Child; Idiopathic Hypereosinophilic Syndrome


Idiopathic hypereosinophilic syndrome is minority in clinical. And more cases were found in male adults while only less cases were found in children. This disease could destroy skin, heart and central never system etc. When the heart was destroyed, it could be named hypereosinophilic carditis. And it also could distroy brain and caused cerebral infarction. As following case, we reported a case of hypereosinophilic carditis combined cerebral infarction in child. The case was a 7 years old boy. Its clinical symptoms were shed tears and sneezing for 20 days, fever for 2 weeks, headache and abdominal pain for 3 days. Eosinophilic cells were 80% of all WBC. Heart echo displaied loffler carditis. Head MRI displaied cerebral infarction. After oral prednison for 4 weeks, the boy came through. This disease had no very effective treatment up to now. The sugar cortical hormone and other immunosuppressant might be effective drugs.

蔺萃, 张永法, 刘海燕. 儿童嗜酸性粒细胞增多性心内膜心肌病伴脑梗塞1例报告[J]. 亚洲儿科病例研究, 2013, 1(3): 53-55.


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