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Titlebook: Neoplastic Diseases of the Blood; Peter H. Wiernik,Janice P. Dutcher,Morie A. Gertz Textbook 2018Latest edition Springer International Pub

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发表于 2025-3-21 18:01:21 | 显示全部楼层 |阅读模式
书目名称Neoplastic Diseases of the Blood
编辑Peter H. Wiernik,Janice P. Dutcher,Morie A. Gertz
视频video
概述Spans the range of hematologic neoplastic disorders from a clinical perspective.Integrates the history, epidemiology, pathology, pathophysiology, therapeutics, and supportive care of neoplastic hemato
图书封面Titlebook: Neoplastic Diseases of the Blood;  Peter H. Wiernik,Janice P. Dutcher,Morie A. Gertz Textbook 2018Latest edition Springer International Pub
描述The new edition of this textbook integrates the history, epidemiology, pathology, pathophysiology, therapeutics, and supportive care of modern neoplastic hematopathology. Now in its sixth edition, this classic and invaluable text brings together a team of internationally renowned experts and offers in-depth coverage of the complex interface between diagnosis and therapy. The textbook is divided into five major sections, with the first four covering the spectrum of hematologic neoplasia, including chronic leukemias and related disorders, acute leukemias, myeloma and related disorders, and lymphomas, and the fifth section covering a variety of topics in supportive care. Chapters are presented in an accessible and easy-to-read layout, providing updates on the tremendous progress made in the last decade in the understanding of the nature of hematologic malignancies and their treatment..Neoplastic Diseases of the Blood, Sixth Edition. is an authoritative and indispensable resource for students, trainees, and clinicians, sure to distinguish itself as the definitive reference on this subject..
出版日期Textbook 2018Latest edition
关键词Chronic Myeloid Leukemia; CLL; Acute Promyelocytic Leukemia; Multiple Myeloma; Non-Hodgkin Lymphoma; Hema
版次6
doihttps://doi.org/10.1007/978-3-319-64263-5
isbn_softcover978-3-030-13261-3
isbn_ebook978-3-319-64263-5
copyrightSpringer International Publishing AG, part of Springer Nature 2018
The information of publication is updating

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发表于 2025-3-22 00:01:40 | 显示全部楼层
Epidemiology and Etiology of Chronic Myeloid Leukemial sparse. CML incidence rates vary from 0.6 to 2.8 cases per 100,000 inhabitants with an obvious increase in age, and men are more often affected than women. Geographic and/or ethnic variations and diagnostic accurateness might contribute to the seen variability. CML can be induced by acute high-dos
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Pathology of the Chronic Myeloid Leukemias, leading to a purely myeloid phenotype, or a lymphoid-myeloid stem cell, potentially giving rise to a mixed phenotype leukemia. These leukemias are categorized partly on the basis of clinicopathological features and partly on the basis of the underlying cytogenetic/molecular genetic abnormalities.
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Morphology and Immunophenotype of Chronic Lymphocytic Leukemia involvement. Lymphadenopathy and proliferation in extramedullary tissues are often seen. The key to the precise diagnosis of CLL begins with assessment of the cytomorphology of the neoplastic cells, often from peripheral blood, but also the architectural patterns of involvement from tissue sections
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The Genomic and Epigenomic Landscape of Chronic Lymphocytic Leukemiadel to understand the processes of cancer progression and evolution. Genome-wide genomic and epigenetic approaches have delivered an unparalleled view of the architecture of the CLL (epi)genome, so that we now possess an extensive catalogue of the copy number, mutational and epigenetic landscape of
发表于 2025-3-23 04:01:20 | 显示全部楼层
Treatment of Chronic Lymphocytic Leukemia and Related Disordersus, and other disease-specific characteristics. According to SEER data, in 2016, there will be 18,960 new cases of CLL diagnosed and more than 100,000 people with CLL living in the USA (.). Fludarabine, cyclophosphamide, and rituximab is an effective regimen in CLL, producing long-term survivors. Ho
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Hairy Cell Leukemia(hairy cells) infiltrating the bone marrow and spleen, leading to pancytopenia, bone marrow fibrosis, and splenic enlargement. Hairy cells have a unique immunophenotypic profile—CD11c+, CD20+, CD25+, and CD103+—that confirms its diagnosis. The course of HCL is usually chronic, but can often be progr
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