作者报告1例海兰组织细胞增生症(简称 SBH)。女性,57岁,因13天前起不规则低热伴面色苍白、头晕、乏力、皮肤出血点及紫癜,体检:中度贫血貌、皮肤散在出血点及紫癜肝肋下12cm,脾肋下5cm。化验:Hb 6.2克,RBC 215万,WBC 7600,分类正常,血小板9.8万;血沉68mm/h,肝功及胎甲球正常,骨髓像增生明显活跃,粒:红为13∶1,全 The authors report a case of Highland Histiocytosis (SBH). Female, 57 years old, irregular and hypothermia with pale complexion, dizziness, weakness, skin bleeds and purpura since 13 days ago. Physical examination: moderate anemia appearance, scattered bleeding spots and purpura liver ribs 12cm, splenic ribs 5cm. Assay: Hb 6.2g, RBC 2150000, WBC 7600, normal classification, platelet 98000; ESR 68mm / h, liver function and normal fetal bone, bone marrow hyperplasia was significantly active, granule: red 13: 1, all