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Clinics in haematology最新文献

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Platelet disorders 血小板疾病
Pub Date : 2018-08-01 DOI: 10.1093/med/9780199568741.003.0282
N. Curry, R. Alikhan
The term ‘platelet disorder’ covers a very large and heterogeneous group of diseases that have a multitude of causes. Platelet disorders are either inherited or acquired and are due to an abnormality of platelet number (quantitative disorder), an abnormality of platelet function (qualitative disorder), or a combination of both. This chapter addresses the causes, diagnosis, and management of platelet disorders.
“血小板紊乱”一词涵盖了一个非常大且异质性的疾病群,这些疾病有多种原因。血小板疾病是遗传性或获得性的,是由于血小板数量异常(定量障碍),血小板功能异常(定性障碍),或两者的组合。本章讨论血小板紊乱的原因、诊断和管理。
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引用次数: 0
Cell Culture Techniques 细胞培养技术
Pub Date : 2011-07-01 DOI: 10.1007/978-1-61779-077-5
Swati Rauthan
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引用次数: 24
The role of colony stimulating factors in leukaemogenesis. 集落刺激因子在白血病发生中的作用。
Pub Date : 1986-11-01
J D Griffin, D C Young
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引用次数: 0
Classification of the myelodysplastic syndromes. 骨髓增生异常综合征的分类。
Pub Date : 1986-11-01 DOI: 10.1007/978-3-642-75952-9_1
J. Bennett
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引用次数: 30
The treatment of myelodysplastic syndromes. 骨髓增生异常综合征的治疗。
Pub Date : 1986-11-01
D R Spriggs, R M Stone, D W Kufe

The available data fail to support a standard therapy for MDS. Any therapy should therefore, include participation in a well designed clinical trial. The MDS include patients with a variety of prognoses. Since most studies show that death from infection and bleeding are more likely than progression to frank leukaemia, attention to supportive care is crucial for all patients with MDS. Some patients with MDS may be successfully supported with transfusions and observation for prolonged periods. Patients with significant comorbid disease or patients without increased marrow myeloblasts are good candidates for this conservative approach. Conversely, young patients have a better likelihood of benefit from aggressive therapy, and intensive chemotherapy or allogenic bone marrow transplantation should be considered. Patients with preleukaemia related to prior cytotoxic therapy are another poor prognosis group for whom aggressive therapy may be the best alternative. Therapy with low-dose ara-C or other differentiating agents should be considered investigational and unproven until comparative trials can demonstrate a definitive survival advantage. In addition to comparative trials, innovative clinical studies are needed to address differentiation as an in vivo mechanism of action and its importance in MDS therapy.

现有的数据不能支持MDS的标准治疗。因此,任何治疗都应包括参与设计良好的临床试验。MDS包括各种预后的患者。由于大多数研究表明,感染和出血导致的死亡比进展为白血病的可能性更大,因此对所有MDS患者的支持性护理的关注至关重要。一些MDS患者可以成功地支持输血和长时间观察。有明显合并症的患者或没有增加骨髓母细胞的患者是这种保守方法的良好候选者。相反,年轻患者从积极治疗中获益的可能性更大,应考虑强化化疗或同种异体骨髓移植。与既往细胞毒性治疗相关的白血病前期患者是另一个预后不良的群体,对他们来说,积极治疗可能是最好的选择。低剂量ara-C或其他分化剂治疗应被认为是研究性和未经证实的,直到比较试验可以证明明确的生存优势。除了比较试验,还需要创新的临床研究来解决分化作为一种体内作用机制及其在MDS治疗中的重要性。
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引用次数: 0
Myelodysplastic syndromes: natural history and features of prognostic importance. 骨髓增生异常综合征:自然史和预后重要性的特征。
Pub Date : 1986-11-01
G J Mufti, D A Galton
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引用次数: 0
5q- and disordered haematopoiesis. 5q-和紊乱的造血。
Pub Date : 1986-11-01
H F Bunn
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引用次数: 0
Chromosome abnormalities in the myelodysplastic syndromes. 骨髓增生异常综合征中的染色体异常。
Pub Date : 1986-11-01
S Heim, F Mitelman
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引用次数: 0
Classification of the myelodysplastic syndromes. 骨髓增生异常综合征的分类。
Pub Date : 1986-11-01
J M Bennett
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引用次数: 0
Myelodysplastic syndromes. 骨髓增生异常综合征。
Pub Date : 1986-11-01
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引用次数: 0
期刊
Clinics in haematology
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