海蓝组织细胞增生症临床及遗传方式的探讨  

Research on Sea Blue Histiocytosis Clinical Findings and Its Hereditary Mode

作　　者：曾宪昌[1] 杨友德[1] 许友芝 许喜泳[1] 曾庆斌[1] 金小君[1] 

机构地区：[1]湖北医学院附二医院

出　　处：《湖北医学院学报》1991年第1期79-83,共5页

摘　　要：本文通过海蓝组织细胞(SBH)增生症一个家系的调查,发现6位患者。对 SBH 进行了细胞化学染色分析,还进行了光镜、位相显微镜荧光显微镜、透射及扫描电镜观察.认为 SBH 增生症的临床表现由 SBH 广泛全身浸润引起,并提出应与反应性 SBH 增生症鉴别.本家系遗传方式为常染色体显性遗传,和其它学者报告不同.Six cases of sea blue histiocytosis were discovered by means of a family line investgation.The analysis of cytochemical staining of sea blue histiocyte was carried out,the observations by optical,phase-contrast,fluorescence micro- scopes and transmission,scanning electron microscopes were also performed. It is suggested that clinical findings of sea blue histiocytosis are due to the general infiltration of SBH in the whole body and difference should be made between it and reactive sea blue histiocytosis.The hereditary mode of this family line is a autosomal dominant inheritance,which differs from those which have been reported.

关 键 词：海蓝组织细胞 增生症 遗传学 

分 类 号：R589.202[医药卫生—内分泌]