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Titlebook: Diagnosis and Management of Myelodysplastic Syndromes; A Clinical Guide Aziz Nazha Book 2020 Springer Nature Switzerland AG 2020 HSCT.CHIP.

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發(fā)表于 2025-3-21 16:07:31 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Diagnosis and Management of Myelodysplastic Syndromes
副標(biāo)題A Clinical Guide
編輯Aziz Nazha
視頻videohttp://file.papertrans.cn/271/270575/270575.mp4
概述Presented in a concise, easy-to-read format.Features over 100 illustrations, photographs, and tables.Written by experts in the field
圖書封面Titlebook: Diagnosis and Management of Myelodysplastic Syndromes; A Clinical Guide Aziz Nazha Book 2020 Springer Nature Switzerland AG 2020 HSCT.CHIP.
描述Myelodysplastic syndromes (MDS) are a group of clonal disorders characterized by pancytopenias and the risk of progression to acute myeloid leukemia. The diagnosis of MDS can be challenging, while the outcomes of MDS patients vary widely. This book provides a concise yet comprehensive overview of MDS..The book begins by reviewing the diagnostic workup of MDS, with a specific focus on the 2016 WHO criteria for MDS diagnosis, and the biology and pathophysiology of the disease. The text then presents the molecular landscape of MDS and its impact on disease diagnosis, prognosis, and treatment decisions. The book continues by profiling different prognostic models of MDS and concludes with a thorough review of treatment algorithms for lower and higher-risk MDS, as well as the use of hematopoietic stem cell transplant to combat the disease..Written by experts in the field,?.Diagnosis and Management of Myelodysplastic Syndromes: A Clinical Guide.?is a valuable resource for clinicians, practitioners, and researchers who are interested in MDS.?The text also features over 100 illustrations, photographs, and tables.?.
出版日期Book 2020
關(guān)鍵詞HSCT; CHIP; CCUS; ICUS; azacitidine; decitabine; lenalidomide
版次1
doihttps://doi.org/10.1007/978-3-030-51878-3
isbn_softcover978-3-030-51880-6
isbn_ebook978-3-030-51878-3
copyrightSpringer Nature Switzerland AG 2020
The information of publication is updating

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MDS Mimics Including CHIP, ICUS, and CCUSns or findings of low specificity. There exist several MDS “mimics” that share findings with MDS but are caused by more benign conditions, other neoplasms, or less well-characterized pre-malignant states. Vitamin and iron deficiencies need to be excluded along with autoimmune conditions, medication
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發(fā)表于 2025-3-22 20:39:41 | 只看該作者
Prognostic Models in Myelodysplastic Syndromestools that take both patient (e.g., age, comorbidities) and disease characteristics (e.g., blast percentage, degree of cytopenias) into account have been developed and are the basis of clinical trial enrollment, patient counseling, and treatment recommendations. Among these clinical-pathologic scori
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發(fā)表于 2025-3-22 22:57:54 | 只看該作者
Treatment Algorithms for Lower-Risk Myelodysplastic Syndromeerized by a low risk of progression to AML, but often prominent anemia. Prognosis of those patients can however be worsened by the presence of myelofibrosis, somatic mutations (except SF3B1 and TET2), resistance to first- and second-line treatments, and comorbidities..Anemia is generally the predomi
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發(fā)表于 2025-3-23 03:23:03 | 只看該作者
Treatment Algorithms for Higher-Risk Diseasel care. While hypomethylating agents (HMAs) have proven clinical and survival benefit in these patients, the only curative treatment remains allogeneic hematopoietic stem cell transplant (HSCT). No regimen has clear superiority in relapsed or refractory higher-risk MDS, and clinical trials (particul
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