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