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5q-syndrome presenting as essential thrombocythemia: myelodysplastic syndrome or chronic myeloproliferative disorders?

作者信息

Koike T, Uesugi Y, Toba K, Narita M, Fuse I, Takahashi M, Shibata A

出版信息

Leukemia. 1995 Mar;9(3):517-8.

PMID:7885050
Abstract
摘要

相似文献

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5q-syndrome presenting as essential thrombocythemia: myelodysplastic syndrome or chronic myeloproliferative disorders?表现为原发性血小板增多症的5q综合征：骨髓增生异常综合征还是慢性骨髓增殖性疾病？
Leukemia. 1995 Mar;9(3):517-8.
2
MDS with del(5q) and associated cKIT D816V positive mastocytosis.伴有5号染色体长臂缺失（del(5q)）及相关cKIT D816V阳性肥大细胞增多症的骨髓增生异常综合征
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Bone marrow morphology in myelodysplastic syndrome associated with isolated del(5q).与孤立性5号染色体长臂缺失相关的骨髓增生异常综合征的骨髓形态学
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Myeloid neoplasm with isolated del(5q) and the MPLW515L mutation fulfills the WHO diagnostic criteria for ET.孤立性 del(5q)和 MPLW515L 突变的骨髓增生异常肿瘤符合 WHO 关于 ET 的诊断标准。
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[Myelodysplastic syndrome associated with 5q deletion, review of 3 cases].[5q 缺失相关的骨髓增生异常综合征，3 例病例回顾]
Tunis Med. 1997 Mar;75(3):127-31.
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Deletion of the long arm of chromosome 5 in essential thrombocythemia.原发性血小板增多症中5号染色体长臂缺失
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Cytogenetic features of 5q deletion and 5q- syndrome in myelodysplastic syndrome in Korea; marker chromosomes proved to be chromosome 5 with interstitial deletion by fluorescence in situ hybridization.韩国骨髓增生异常综合征中5q缺失和5q-综合征的细胞遗传学特征；荧光原位杂交证实标记染色体为存在间质缺失的5号染色体。
Cancer Genet Cytogenet. 2010 Dec;203(2):193-202. doi: 10.1016/j.cancergencyto.2010.08.007.
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5q- syndrome presenting chronic myeloproliferative disorders-like manifestation: a case report.
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Efficacy of lenalidomide treatment and complete cytogenetic remission in a case of myelodysplastic syndrome with del(5q) and del(9q).来那度胺治疗伴有del(5q)和del(9q)的骨髓增生异常综合征患者的疗效及细胞遗传学完全缓解情况
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Myelodysplastic syndromes associated with interstitial deletion of chromosome 5q: clinicopathologic correlations and new insights from the pre-lenalidomide era.与5号染色体长臂间质性缺失相关的骨髓增生异常综合征：临床病理相关性及来那度胺治疗前时代的新见解
Am J Hematol. 2008 Sep;83(9):708-13. doi: 10.1002/ajh.21245.

引用本文的文献

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Cytogenetic abnormalities in essential thrombocythemia at presentation and transformation.原发性血小板增多症初诊时和转化后的细胞遗传学异常。
Int J Hematol. 2009 Nov;90(4):522-525. doi: 10.1007/s12185-009-0411-5. Epub 2009 Aug 29.
2
Clinical and pathological criteria for the diagnosis of essential thrombocythemia, polycythemia vera, and idiopathic myelofibrosis (agnogenic myeloid metaplasia).原发性血小板增多症、真性红细胞增多症和原发性骨髓纤维化（特发性髓样化生）诊断的临床及病理标准。
Int J Hematol. 2002 Aug;76(2):133-45. doi: 10.1007/BF02982575.