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The 2016 revision of the World Health Organization classification of lymphoid neoplasms

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TLDR
The revision clarifies the diagnosis and management of lesions at the very early stages of lymphomagenesis, refines the diagnostic criteria for some entities, details the expanding genetic/molecular landscape of numerous lymphoid neoplasms and their clinical correlates, and refers to investigations leading to more targeted therapeutic strategies.
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This article is published in Blood.The article was published on 2016-05-19 and is currently open access. It has received 5321 citations till now.

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Chronic lymphocytic leukemia treatment algorithm 2018

TL;DR: The ability to risk stratify CLL patients continues to evolve; the CLL-International Prognostic Index (CLL-IPI) is the best validated tool in predicting time to first therapy among previously untreated patients.
Journal ArticleDOI

The 2016 updated WHO classification of lymphoid neoplasias

TL;DR: The aim of this revised version of the 4th edition of the WHO classification of tumors of the hematopoietic and lymphoid tissue is to incorporate the new scientific and clinical information to refine diagnostic criteria for previously described lymphomas, in some cases, change nomenclature to convey better the clinical features of the disease.
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CREBBP/EP300 mutations promoted tumor progression in diffuse large B-cell lymphoma through altering tumor-associated macrophage polarization via FBXW7-NOTCH-CCL2/CSF1 axis.

TL;DR: In this paper, the authors investigated the biological relevance of epigenetic gene mutations on tumor microenvironment and found that mutations in CREBBP/EP300 were associated with decreased peripheral blood absolute lymphocyte-to-monocyte ratios and inferior progression-free and overall survival.
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Epstein-Barr Virus-Associated Lymphoproliferative Disorders: Review and Update on 2016 WHO Classification.

TL;DR: This article reviews the current evidence covering EBV-associated LPDs based on the 2016 classification of the World Health Organization and explains why it is important to understand their unique pathophysiology for correct diagnoses and optimal management.
References
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WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues

TL;DR: Thank you very much for reading who classification of tumours of haematopoietic and lymphoid tissues, and maybe you have knowledge that, people have look hundreds of times for their chosen readings like this, but end up in malicious downloads.
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The 2008 WHO classification of lymphoid neoplasms and beyond: evolving concepts and practical applications.

TL;DR: The criteria and significance of early or precursor lesions and the identification of certain lymphoid neoplasms largely associated with particular age groups, such as children and the elderly are addressed, and the issue of borderline categories having overlapping features with large B-cell lymphomas is reviewed.
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Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

TL;DR: The patterns of somatic mutation, supported by functional and clinical analyses, strongly indicate that the recurrent NOTCH1, MYD88 and XPO1 mutations are oncogenic changes that contribute to the clinical evolution of the disease.
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MYD88 L265P Somatic Mutation in Waldenström's Macroglobulinemia

TL;DR: MYD88 L265P is a commonly recurring mutation in patients with Waldenström's macroglobulinemia that can be useful in differentiating WaldenStröm’s macrogalobulinesia and non-IgM LPL from B-cell disorders that have some of the same features.
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