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同胞姐弟同患海蓝组织细胞综合征2例报告并文献复习 被引量:2

Sea-blue Histiocytic Syndrome in Sister and Brother and Review of Literature
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摘要 目的:探讨海蓝组织细胞综合征(SBH)的临床及血液学特点。方法:对2例同患SBH姐弟的临床资料进行分析,并对文献进行复习。结果:2例同属原发性家族性SBH,具有典型的SBH的临床及血液学特点。结论:此病少见,临床易误诊,注意鉴别诊断,以基础治疗为基础。 Objective :To discuss the clinical and haematological characteristics of sea-blue histiocytic syndrome (SBH.). Methods:To analyse the clinical materials of two cases of SBH and then to review the literature. Results:The two cases belong to idiopathic familial SBH,and they had the typical characteristics of clinic and haematology. Conclusions:the disease is very rare and is easily misdiagnosed, the doctor should distinguish them,the sufferer should be taken the support treatment as the foundation.
出处 《中国误诊学杂志》 CAS 2006年第14期2670-2672,共3页 Chinese Journal of Misdiagnostics
关键词 海蓝组织细胞综合征/遗传学 同胞 Sea-blue histiocyte syndrome/genetics Siblings
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参考文献14

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共引文献10

同被引文献14

  • 1刘平毅,陈玉云,林兴明.同胞姐弟同患海蓝组织细胞增生症并文献复习[J].山东医学高等专科学校学报,2006,28(4):263-264. 被引量:1
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  • 9李彦旭,郭涛,聂秀,杨秀萍,安丹,柴新群.脾切除术治疗海蓝组织细胞增多症1例[J].肝胆胰外科杂志,2008,20(6):399-399. 被引量:4
  • 10李惠珍,杨生义,李维,周小平,白萱.乙型肝炎肝硬化合并海蓝组织细胞增生症1例报告[J].实用肝脏病杂志,2013,16(6):565-566. 被引量:3

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