Myeloproliferative disorders "Philadelphia negative" and JAK2V617F mutation: study of 15 cases in Togo

被引:0
作者
Padaro, Essohana [1 ]
Agbetiafa, Kossi [1 ]
Kueviakoe, Irenee Messanh Delagnon [1 ]
Layibo, Yao [1 ]
Amegbor, Koffi [2 ]
Vovor, Ahoefa [3 ]
Giraudier, Stephane [4 ]
Sanogo, Ibrahima [5 ]
Segbena, Akuete Yvon [1 ]
机构
[1] Univ Lome, Serv Hematol, Lome, Togo
[2] Univ Lome, CHU Tokoin, Serv Anat Pathol, Lome, Togo
[3] Univ Lome, CHU Tokoin, Serv Hematol, Lome, Togo
[4] Univ Paris 12, Serv Hematol Biol, APHP Henri Mondor, Creteil, France
[5] Univ Cocody, CHU Yopougon, Serv Hematol Clin, Abidjan, Cote Ivoire
关键词
myeloproliferative syndrome; negative Chromosom Philadelphia; JAK2; change; Togo; TYROSINE KINASE JAK2; POLYCYTHEMIA-VERA; ACQUIRED MUTATION; THROMBOCYTHEMIA; DIAGNOSIS; NEOPLASMS;
D O I
10.1684/abc.2012.0747
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The goal of our study is to document the prevalence of change JAK2V617F among patients reached of myeloproliferative syndromes (MPS) in Togo in order to evaluate frequencies. This descriptive study included 15 patients followed with the CHU Campus for a SMP. The research of JAK2 change by PCR was carried out with the APHP Henri Mondor of Creteil (France). During the study period, 15 patients followed for MPS (9 cases of polycythemia Vera, 5 cases of essential thrombocytemia and a case of primitive myelofibrosis) profited from the research of JAK2 change. The Middle age of the patients was respectively of 45 +/- 18 years; of 55 +/- 6 years for the PV and the essential thrombocytemia. The patient followed for primitive myelofibrosis was 72 years old. Sex-ratio (H/F) was of 2. JAK2 Change was positive in 5 cases out of 9 (55.5%) of the polycythemia Vera, at 3 patients out of 5 (60%) followed for essential thrombocytemia but negative for patient reached of primitive myelofibrosis. In conclusion, JAK2 Change has an interest diagnosis and forecast in the MPS negative Chromosom Philadelphia and can be systematic even in Africa Sub-saharian.
引用
收藏
页码:591 / 594
页数:4
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