Maaroufi Hicham El, Ababou Mounir, Hammani Adnane, Ahchouch Siham, Jennane Salim, Mahtat Mehdi, Mikdmae Mohamed, Messaoudi Nezha, Doghmi Kamal
Service d´Hématologie Clinique, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Laboratoire d´Hématologie, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Pan Afr Med J. 2020 Dec 2;37:300. doi: 10.11604/pamj.2020.37.300.20972. eCollection 2020.
We conducted a retrospective descriptive analytical study in the Department of Clinical Haematology at the Mohammed V Military Training Hospital in Rabat over a period of 10 years. This study included 76 patients diagnosed with myelodysplastic syndrome (MDS) between 2008 and 2018. The average number of cases per year was 7.6. Out of 76 patients, 57% were men and 43% were women. The average age of our study population was 65.75 ± 12.55. The average age was 66.88 ± 13.10. No cases of profession exposed to disease was reported. Ninety-seven point three percent of patients had primary myelodysplastic syndrome and only 2 or 2.7% had myelodysplastic syndrome secondary to chemotherapy. The average time between the first visit and the diagnosis of myelodysplastic syndrome was, on average, 33.6 days ± 51, with a median of 19 days. The IPSS prognostic score was: low risk in 37.4% of cases, intermediate risk 1 in 46.6% of cases, intermediate risk in 12% of cases and high risk in 4% of cases. Thus, 84% of patients had low-risk MDS and 16% had high-risk MDS. Regular monitoring of patients showed many complications such as bleeding in 13% of patients, infections in 8% of cases, secondary hemochromatosis as a result of iterative transfusions in 6.6% of patients and transformation to acute myeloid leukemia in 2.7% of patients. In our study, abstention was the therapeutic choice in 42.1% of patients, transfusion was recommended in 35.5% of patients: red cells in 70% of cases, platelet concentrates in 40% of cases, iron chelators in 25% of transfused patients and EPO in 27% of patients. azacitidine was prescribed in 18% of patients, 50% had low-risk MDS and 50% had high-risk MDS. Bone marrow transplant was the only curative treatment for MDS. It was performed in a single patient with high risk MDS.
我们在拉巴特穆罕默德五世军事训练医院临床血液科进行了一项为期10年的回顾性描述性分析研究。该研究纳入了2008年至2018年间确诊为骨髓增生异常综合征(MDS)的76例患者。每年的平均病例数为7.6例。76例患者中,57%为男性,43%为女性。我们研究人群的平均年龄为65.75±12.55岁。平均年龄为66.88±13.10岁。未报告有职业暴露于该疾病的病例。97.3%的患者患有原发性骨髓增生异常综合征,仅有2例(占2.7%)患有化疗继发的骨髓增生异常综合征。首次就诊至骨髓增生异常综合征诊断的平均时间为33.6天±51天,中位数为19天。国际预后评分系统(IPSS)预后评分情况为:低危病例占37.4%,中危-1病例占46.6%,中危病例占12%,高危病例占4%。因此,84%的患者患有低危MDS,16%的患者患有高危MDS。对患者的定期监测显示出许多并发症,如13%的患者出现出血,8%的病例发生感染,6.6%的患者因反复输血导致继发性血色素沉着症,2.7%的患者转化为急性髓系白血病。在我们的研究中,42.1%的患者选择不治疗,35.5%的患者建议输血:70%的病例输注红细胞,40%的病例输注血小板浓缩物,25%的输血患者使用铁螯合剂,27%的患者使用促红细胞生成素(EPO)。18%的患者使用阿扎胞苷,其中50%为低危MDS,50%为高危MDS。骨髓移植是MDS唯一的治愈性治疗方法。仅1例高危MDS患者接受了骨髓移植。