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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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T-cell Lymphoma Epidemiology: the Known and Unknown

TL;DR: Current epidemiologic and prognostic factors data associated with the individual subtypes both of peripheral T-cell lymphoma and cutaneous T- cell lymphoma found in large cohort and case studies are reported on.
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Biomarker-driven strategy for MCL1 inhibition in T-cell lymphomas

TL;DR: MCL1 inhibition is a promising strategy as both a single agent and in combination with chemotherapy for patients with TCL and functional dependence on MCL1 and the combination of AZD5991 and CHOP achieved synergy based on survival improvement beyond a mathematical "sum of benefits" model.
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The aetiology of B‐cell lymphoid malignancies with a focus on chronic inflammation and infections

TL;DR: The latest developments in the aetiology of B‐cell lymphoid malignancy subtypes focusing on immune perturbation are summarized, linking several subtypes to variations in the human leucocyte antigen (HLA) class genes.
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Aptamer based recognition of cancer cells: Recent progress and challenges in bioanalysis

TL;DR: This review summarizes advances from 2010 to June 2020 in the development of aptasensors for cancer cell detection, and addresses the remaining challenges and opportunities to integrate aptasensing platforms into point-of-care solutions.
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CLIPPERS and its mimics: evaluation of new criteria for the diagnosis of CLIPPERS

TL;DR: This study highlights that nodular enhancement should be considered more as an unusual finding than a red flag excluding the diagnosis of CLIPPERS; red flags may occur up to 18 months after disease onset; and brain biopsy should target an atypical enhancing lesion when non-invasive investigations remain inconclusive.
References
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Book

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.
Journal ArticleDOI

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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