白塞病合并骨髓增生异常综合征(MDS)相对少见,国内至1998年共报告11例。我院近4年遇到3例,报告如下。 1 病例报告 1.1 例1.女,34岁。反复口腔、眼部、会阴部位溃疡1年余,于1999—09—13就诊。查体:体温36.5℃,贫血貌,浅表淋巴结不大,口腔及会阴部位多发性溃疡。肝、脾肋下未触及。双肘、踝关节红肿热痛。实验室检查:白细胞2.9×10~9/L,分类未见原始粒单细胞,血红蛋白97g/L, Behcet’s disease with myelodysplastic syndrome (MDS) is relatively rare, a total of 11 cases were reported in China. Nearly 4 years in our hospital encountered three cases, the report is as follows. 1 case report 1.1 cases 1. Female, 34 years old. Repeated oral, ocular, perineal ulcers more than 1 year, in 1999-09-13 treatment. Physical examination: body temperature 36.5 ℃, anemia, superficial lymph nodes, oral and perineal multiple ulcers. Liver, spleen ribs untouched. Double elbow, ankle swelling and heat pain. Laboratory tests: white blood cells 2.9 × 10 ~ 9 / L, no primary classification of single cells, hemoglobin 97g / L,