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海兰组织细胞增生症(Sea blue histiocyto-sis 简称 SBH),亦称海兰组织细胞综合征(Seablue histiocytosis syndrome)。1954年 Sawi-tsky 等首次描述,1970年 Silverstein 总结39例,国内自1980年陆定伟首次报道以来,至1986年共报道22例,本文报道1例。病历摘要女患,32岁。1979年初自觉头晕,乏力,手足麻木感;血红蛋白95g/L。1982年发现脾肋下1.0cm。1985年间断出现齿龈出血、皮肤紫癜、诊断血小板减少性紫癜,为进一步确诊而来我所就诊。体检:巩膜无黄染,表浅淋巴结不肿大,双肺呼吸
Sea blue histiocyto-sis (Sea blue histiocyto-sis referred to as SBH), also known asHeland tissue cell syndrome (Seablue histiocytosis syndrome). First described by Sawi-tsky et al in 1954, Silverstein summed up 39 cases in 1970. Since Lu Dingwei first reported in 1980, 22 cases were reported in 1986, and 1 case was reported in this paper. Female patient history, 32 years old. Early 1979, dizziness, fatigue, numbness of hands and feet; hemoglobin 95g / L. In 1982 found 1.0cm spleen ribs. 1985 intermittent bleeding gums, purpura skin, diagnosis of thrombocytopenic purpura, for further diagnosis come to my clinic. Physical examination: Sclera no yellow dye, superficial lymph nodes not swollen, lungs breathing