Bing-Neel Syndrome with Detectable MYD88 L265P Gene Mutation as a Late Relapse Following Autologous Hematopoietic Stem Cell Transplantation for Waldenström's Macroglobulinemia.
作者信息
Kopińska Anna J, Helbig Grzegorz, Koclęga Anna, Kyrcz-Krzemień Sławomira
机构信息
Silesia University Faculty of Medicine in Katowice, Department of Hematology and Bone Marrow Transplantation, Katowice, Poland Phone: +48322591310 E-mail:
出版信息
Turk J Haematol. 2017 Jun 5;34(2):186-187. doi: 10.4274/tjh.2016.0452.
Abstract
摘要
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Bing-Neel Syndrome with Detectable MYD88 L265P Gene Mutation as a Late Relapse Following Autologous Hematopoietic Stem Cell Transplantation for Waldenström's Macroglobulinemia.伴可检测到MYD88 L265P基因突变的宾-尼尔综合征作为华氏巨球蛋白血症自体造血干细胞移植后的晚期复发
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本文引用的文献
1
Guideline for the diagnosis, treatment and response criteria for Bing-Neel syndrome.宾-尼尔综合征的诊断、治疗及反应标准指南。
Haematologica. 2017 Jan;102(1):43-51. doi: 10.3324/haematol.2016.147728. Epub 2016 Oct 6.
2
Bing Neel Syndrome in a Previously Untreated Patient With Waldenström's Macroglobulinemia: Contribution of MYD88 L265P Mutation on Cerebrospinal Fluid.一名既往未治疗的华氏巨球蛋白血症患者的宾尼尔综合征：MYD88 L265P突变在脑脊液中的作用
Clin Lymphoma Myeloma Leuk. 2016 Jan;16(1):e7-9. doi: 10.1016/j.clml.2015.11.004. Epub 2015 Dec 2.
3
Efficacy of ibrutinib in the treatment of Bing-Neel syndrome.依鲁替尼治疗宾-尼尔综合征的疗效。
Am J Hematol. 2016 Mar;91(3):E17-9. doi: 10.1002/ajh.24279.
4
Central nervous system involvement by Waldenström macroglobulinaemia (Bing-Neel syndrome): a multi-institutional retrospective study.华氏巨球蛋白血症累及中枢神经系统（宾 - 尼尔综合征）：一项多机构回顾性研究
Br J Haematol. 2016 Mar;172(5):709-15. doi: 10.1111/bjh.13883. Epub 2015 Dec 21.
5
Bing-Neel syndrome, a rare complication of Waldenström macroglobulinemia: analysis of 44 cases and review of the literature. A study on behalf of the French Innovative Leukemia Organization (FILO).宾-尼尔综合征，一种华氏巨球蛋白血症的罕见并发症：44例病例分析及文献综述。一项代表法国创新白血病组织（FILO）开展的研究。
Haematologica. 2015 Dec;100(12):1587-94. doi: 10.3324/haematol.2015.133744. Epub 2015 Sep 18.
6
Recurrent mutations of CD79B and MYD88 are the hallmark of primary central nervous system lymphomas.CD79B和MYD88的复发性突变是原发性中枢神经系统淋巴瘤的标志。
Neuropathol Appl Neurobiol. 2016 Apr;42(3):279-90. doi: 10.1111/nan.12259. Epub 2015 Jul 20.
7
MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome.MYD88 L265P 突变有助于宾-尼尔综合征的诊断。
Br J Haematol. 2014 Nov;167(4):506-13. doi: 10.1111/bjh.13078. Epub 2014 Aug 27.
8
MYD88 L265P somatic mutation in Waldenström's macroglobulinemia.瓦尔登斯特伦巨球蛋白血症中的 MYD88 L265P 体细胞突变。
N Engl J Med. 2012 Aug 30;367(9):826-33. doi: 10.1056/NEJMoa1200710.
9
Waldenström's macroglobulinemia.华氏巨球蛋白血症
Oncologist. 2000;5(1):63-7. doi: 10.1634/theoncologist.5-1-63.
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