天津医药 ›› 2018, Vol. 46 ›› Issue (7): 760-764.doi: 10.11958/20171352

• 诊断技术 • 上一篇    下一篇

儿童特发性高嗜酸粒细胞增多综合征一例及文献复习

王晶瑶,赵煜△   

  1. 天津市儿童医院消化科(邮编300134)
  • 收稿日期:2017-11-29 修回日期:2018-05-18 出版日期:2018-07-15 发布日期:2018-07-15
  • 通讯作者: 王晶瑶 E-mail:404862256@qq.com
  • 作者简介:王晶瑶(1985),女,硕士,主要从事小儿消化内科方面研究

Case report of one child with idiopathic hypereosinophilic syndrome and literature review

WANG Jing-yao,ZHAO Yu△   

  1. Department of Gastroenterology, Tianjin Children’s Hospital, Tianjin 300134, China △Corresponding Author E-mail: zhaoyu1617@126.com
  • Received:2017-11-29 Revised:2018-05-18 Published:2018-07-15 Online:2018-07-15
  • Contact: Jing-Yao WANG E-mail:404862256@qq.com

摘要: 特发性高嗜酸粒细胞增多综合征(IHES)以骨髓、外周血和组织中嗜酸性粒细胞增高及多脏器受损为主要 特征,发生在儿童中极为罕见。现报道1例8岁的IHES女性患儿,以腹胀、呕吐为首发症状,影像学检查发现消化道、 膀胱、肺受累,血常规示嗜酸性粒细胞 20.64×109/L,骨髓涂片示成熟嗜酸性粒细胞比例 32%,FIP1L1/PDGFRA、 FGFR1、IGH等基因检测,寄生虫、自身抗体等检测均阴性,诊断考虑为IHES,给予激素治疗后嗜酸性粒细胞明显下 降,症状缓解,虽后有病情反复,但是仍对激素敏感。后附文献分析及国内的相关个案报道。

关键词: 少见病, 高嗜酸粒细胞增多综合征, 特发性, 儿童

Abstract: Idiopathic hypereosinophilic syndrome (IHES) is a very rare disorder in children, characterized by increased eosinophils in bone marrow, peripheral blood and tissue, resulting in multiple organ damage. We report a case of an 8-yearold girl with IHES, whose initial complaints were diarrhea and abdominal distension. Image examinations indicated that the digestive tract, lung and urinary bladder were all affected. Routine blood test showed that the eosinophilia was 20.64×109/L. Bone marrow smear showed that the mature eosinophilic granulocytes increased to 32%. The FIL1P1/PDGFRA, FGFR1 and IGH gene detection, parasites and antibody tests were all negative. The diagnosis of IHES was considered. The eosinophil decreased significantly and symptoms relieved after steroid treatment, though with recurrences, steroids were still sensitive. Then we reviewed the relevant literature and cases of children with IHES in China.

Key words: rare diseases, hypereosinophilic syndrome, idiopathic, child