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Titlebook: Rare Lymphomas; Martin Dreyling,Michael E. Williams Book 2014 Springer-Verlag Berlin Heidelberg 2014 Malignant Lymphoma.Molecular Pathogen

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書(shū)目名稱(chēng)Rare Lymphomas
編輯Martin Dreyling,Michael E. Williams
視頻videohttp://file.papertrans.cn/822/821259/821259.mp4
概述Focuses on the rare lymphomas often not covered in other books.Provides a comprehensive overview of current treatment strategies.Emphasizes translation of molecular science into clinical care.Most cha
叢書(shū)名稱(chēng)Hematologic Malignancies
圖書(shū)封面Titlebook: Rare Lymphomas;  Martin Dreyling,Michael E. Williams Book 2014 Springer-Verlag Berlin Heidelberg 2014 Malignant Lymphoma.Molecular Pathogen
描述After a decade of tremendous progress in the diagnostic and therapeutic approaches to malignant lymphoma, optimal treatment strategies are now based not only on accurate diagnosis but also on thorough evaluation of clinical and molecular risk factors. Even more importantly, molecular targeted approaches have been shown to be effective in the treatment of distinct lymphoma subtypes. Against this background, clinical management of especially the rare lymphomas remains a challenge for the general oncologist. This book provides a comprehensive overview of current treatment strategies in these rare lymphoma subtypes. Experts in the field from around the world describe histomorphology in a clinically relevant manner, consider the role of risk factors in detail, and discuss the spectrum of therapeutic approaches. Special emphasis is placed on the translation of molecular science into clinical care, and a disease-specific algorithm is proposed for each entity.
出版日期Book 2014
關(guān)鍵詞Malignant Lymphoma; Molecular Pathogenesis; Targeted Approaches
版次1
doihttps://doi.org/10.1007/978-3-642-39590-1
isbn_softcover978-3-662-50772-8
isbn_ebook978-3-642-39590-1Series ISSN 2197-9766 Series E-ISSN 2197-9774
issn_series 2197-9766
copyrightSpringer-Verlag Berlin Heidelberg 2014
The information of publication is updating

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Molecular Genetics of Rare Lymphomas behavior. Recent improvements in pathologic diagnosis as well as the application of novel molecular biological techniques in clinical routine have led to the distinction of various subtypes of malignant lymphoma that occur at rather low frequencies. These lymphoma subtypes are here referred to as “
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Cutaneous T-Cell Lymphomaoming T lymphocytes. Clinically, they appear in considerable variability as cutaneous lesions, but mostly without signs of further nodal or systemic involvement and in many instances they keep confined to the skin for a indefinite time. Historically, mycosis fungoides (MF) and Sézary syndrome (SS) h
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Primary Mediastinal Large B-Cell Lymphomastitutes 6–10 % of all diffuse large B-cell lymphomas (DLBCL), occurring more often in young females. It is characterised by a diffuse proliferation of medium to large B cells associated with sclerosis and a degree of compartmentalisation. CD30 staining is observed in the vast majority of cases (~80
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