Mouhib Hanane, K. Ilham, Hanane Zahir, Yahyaoui Hicham, A. A. Mustapha, C. Mohammed
{"title":"马拉喀什阿维森纳军事医院实验室骨髓增生异常综合征的经验","authors":"Mouhib Hanane, K. Ilham, Hanane Zahir, Yahyaoui Hicham, A. A. Mustapha, C. Mohammed","doi":"10.11648/J.AJLM.20190406.16","DOIUrl":null,"url":null,"abstract":"MDS are clonal disorders of multipotent or myeloid stem cells. The disease is characterized by inefficient hematopoiesis responsible for peripheral cytopenias and contrasting with a rich marrow. The natural course of this disease is acute myeloid leukemia (AML). This is a retrospective study on the files of patients who had a haematological assessment at the laboratory of the military hospital Avicenna Marrakech between July 2014 and July 2018 for a duration of 4 years. Included in our study were all patients with documented myelodysplasia. The average age of patients is 63.63 years with extremes of 19 years and 89 years; the sex ratio was 1.3 (17 men and 13 women). NFS was abnormal in all patients, 96.66% of whom had anemia. The myelogram was performed in all patients and allowed the diagnosis of MDS in 90% of cases. Our study shows that management needs to be further improved by selecting high-risk MDS patients, potentially candidates for allogeneic hematopoietic stem cell transplantation.","PeriodicalId":320526,"journal":{"name":"American Journal of Laboratory Medicine","volume":"29 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Myelodysplastic Syndromes Experience of the Laboratory of the Military Hospital Avicenna Marrakech\",\"authors\":\"Mouhib Hanane, K. Ilham, Hanane Zahir, Yahyaoui Hicham, A. A. Mustapha, C. Mohammed\",\"doi\":\"10.11648/J.AJLM.20190406.16\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"MDS are clonal disorders of multipotent or myeloid stem cells. The disease is characterized by inefficient hematopoiesis responsible for peripheral cytopenias and contrasting with a rich marrow. The natural course of this disease is acute myeloid leukemia (AML). This is a retrospective study on the files of patients who had a haematological assessment at the laboratory of the military hospital Avicenna Marrakech between July 2014 and July 2018 for a duration of 4 years. Included in our study were all patients with documented myelodysplasia. The average age of patients is 63.63 years with extremes of 19 years and 89 years; the sex ratio was 1.3 (17 men and 13 women). NFS was abnormal in all patients, 96.66% of whom had anemia. The myelogram was performed in all patients and allowed the diagnosis of MDS in 90% of cases. Our study shows that management needs to be further improved by selecting high-risk MDS patients, potentially candidates for allogeneic hematopoietic stem cell transplantation.\",\"PeriodicalId\":320526,\"journal\":{\"name\":\"American Journal of Laboratory Medicine\",\"volume\":\"29 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-12-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Laboratory Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.11648/J.AJLM.20190406.16\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Laboratory Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11648/J.AJLM.20190406.16","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Myelodysplastic Syndromes Experience of the Laboratory of the Military Hospital Avicenna Marrakech
MDS are clonal disorders of multipotent or myeloid stem cells. The disease is characterized by inefficient hematopoiesis responsible for peripheral cytopenias and contrasting with a rich marrow. The natural course of this disease is acute myeloid leukemia (AML). This is a retrospective study on the files of patients who had a haematological assessment at the laboratory of the military hospital Avicenna Marrakech between July 2014 and July 2018 for a duration of 4 years. Included in our study were all patients with documented myelodysplasia. The average age of patients is 63.63 years with extremes of 19 years and 89 years; the sex ratio was 1.3 (17 men and 13 women). NFS was abnormal in all patients, 96.66% of whom had anemia. The myelogram was performed in all patients and allowed the diagnosis of MDS in 90% of cases. Our study shows that management needs to be further improved by selecting high-risk MDS patients, potentially candidates for allogeneic hematopoietic stem cell transplantation.