Hu Xi-Mei, Fan Zhi-Rong, Zhou Shui-Yang, Wei Wei, Zhu Bi-Hui, Cao Yun-Fang
Department of Hematology, Songjiang District Center Hospital, Shanghai 201600, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2004 Apr;12(2):170-3.
To investigate the hematological abnormality and clinical characteristics in systemic lupus erythematosus (SLE), the hematological data of 58 SLE and the curative effects of corticosteroid and immunosuppressive agents on SLE were retrospectively analysed by using SPSS/PC software. The results showed that the incidence of hematological abnormalities in 58 cases was as follows: 50 cases of hemogram abnormality (86.2%), 41 of anemia (70.7%), 34 of thrombocytopenia (58.7%), 37 of leukopenia (63.8%). Peripheral cytopenia of every cell lineage was common in SLE. The cell abnormalities of two or three lineages were seen in 41 cases (70.7%). The initial symptoms with hematological abnormality were found in 12 cases (20.7%), 7 out of 12 cases were erroneously diagnosed as hematology diseases (12.1%). In 30 out of 58 patients, the results of bone marrow examination showed that 23 had hyperplasia (76.7%) and 7 were hypoplasia. In 25 out of 38 cases, splenomegaly (65.8%) was found by B ultrasonography. In 25 patients with SLE receiving Coombs test, 3 were positive (12.0%). PAIg increased in 16 out of 22 cases of thrombocytopenia (72.7%). 26 cases of SLE with two or three lineage cytopenia in peripheral blood were treated by corticosteroid and immunosuppressive agent. The hemogram improved in all patients including 6 cases of bone marrow hypoplasia. It is concluded that the hematological abnormalities are frequent in SLE patients, which are short of specialty. The cytopenia of two or more lineage in peripheral blood is most common when bone marrow shows hyperplastic. The therapy with corticosteroid and immunosuppressive agents is efficacious.
为探讨系统性红斑狼疮(SLE)患者血液学异常情况及临床特点,采用SPSS/PC软件对58例SLE患者的血液学资料及糖皮质激素和免疫抑制剂对SLE的疗效进行回顾性分析。结果显示,58例患者血液学异常发生率如下:血常规异常50例(86.2%),贫血41例(70.7%),血小板减少34例(58.7%),白细胞减少37例(63.8%)。SLE患者外周血各细胞系减少较为常见。41例(70.7%)患者出现两系或三系细胞异常。12例(20.7%)患者以血液学异常为首发症状,其中7例(12.1%)曾被误诊为血液系统疾病。58例患者中30例行骨髓检查,结果显示23例增生(76.7%),7例增生减低。38例患者中行B超检查,25例(65.8%)发现脾大。25例SLE患者行Coombs试验,3例阳性(12.0%)。22例血小板减少患者中16例(72.7%)PAIg升高。对26例外周血两系或三系血细胞减少的SLE患者采用糖皮质激素和免疫抑制剂治疗。所有患者血常规均有改善,包括6例骨髓增生减低患者。结论:SLE患者血液学异常较为常见,缺乏特异性。外周血两系或以上血细胞减少最为常见,骨髓多表现为增生。糖皮质激素和免疫抑制剂治疗有效。