短暂性无脾症与纯红细胞再生障碍性贫血并存。
Concurrence of transient asplenia and pure red cell aplasia.
作者信息
Ozkaynak M F, Ortega J A, Miller J
机构信息
Division of Hematology/Oncology, Children's Hospital of Los Angeles.
出版信息
Eur J Pediatr. 1990 May;149(8):542-4. doi: 10.1007/BF01957688.
PMID:2112092
Abstract
We report a 9-year-old male with anatomical asplenia diagnosed at 7 months of age documented by ultrasound and liver-spleen scan which resolved spontaneously 3 years later. The patient concurrently had pure red cell aplasia which subsequently resolved spontaneously.
摘要
我们报告一例9岁男性，其在7个月大时经超声和肝脾扫描诊断为解剖学无脾症，3年后自发缓解。该患者同时患有纯红细胞再生障碍性贫血，随后也自发缓解。
Zotero 插件