The 2016 revision of the World Health Organization classification of lymphoid neoplasms
Steven H. Swerdlow,Elias Campo,Stefano Pileri,Nancy L. Harris,Harald Stein,Reiner Siebert,Ranjana H. Advani,Michele Ghielmini,Gilles Salles,Andrew D. Zelenetz,Elaine S. Jaffe +10 more
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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.About:
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.read more
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Baseline 18F-FDG PET radiomic features as predictors of 2-year event-free survival in diffuse large B cell lymphomas treated with immunochemotherapy
Nicolas Aide,Nicolas Aide,Christophe Fruchart,Catherine Nganoa,Anne-Claire Gac,Charline Lasnon +5 more
TL;DR: 18F-FDG PET heterogeneity of the largest lymphoma lesion is an independent predictor of 2y-EFS in newly diagnosed DLBCL treated with immunochemotherapy, and metabolic heterogeneity emerges as a new tool for survival prognostication of patients and has been explored in many solid tumours with promising results.
Journal ArticleDOI
Feline low-grade alimentary lymphoma: an emerging entity and a potential animal model for human disease
Mathieu Victor Paulin,Lucile Couronné,Lucile Couronné,Jérémy Béguin,Sophie Le Poder,Maxence Delverdier,Marie-Odile Semin,Julie Bruneau,Julie Bruneau,Nadine Cerf-Bensussan,Nadine Cerf-Bensussan,Georgia Malamut,Georgia Malamut,Christophe Cellier,Christophe Cellier,G. Benchekroun,Laurent Tiret,Alexander J. German,Olivier Hermine,Olivier Hermine,Valérie Freiche +20 more
TL;DR: Feline LGAL could be considered to be a potential animal model for indolent digestive T-cell lymphoproliferative disorder, a rare condition in human medicine.
Journal ArticleDOI
Spanish Guidelines for Diagnosis, Management, Treatment, and Prevention of DRESS Syndrome.
Rosario Cabañas,Elena Ramírez,Elena Sendagorta,Remedios Alamar,R. Barranco,Natalia Blanca-López,Inmaculada Doña,Javier Fernández,Ignacio Garcia-Nunez,J García-Samaniego,R Lopez-Rico,E Marín-Serrano,C Mérida,MC Moya,N R Ortega-Rodríguez,B Rivas Becerra,Patricia Rojas-Pérez-Ezquerra,M J Sánchez-González,C Vega-Cabrera,C Vila-Albelda,Teresa Bellón +20 more
TL;DR: The first Spanish guidelines on DRESS syndrome are now being published and important aspects as practical recommendations about clinical diagnosis, identification of the culprit drug through the Spanish pharmacovigilance system algorithm and allergy study have been addressed.
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High-resolution architecture and partner genes of MYC rearrangements in lymphoma with DLBCL morphology.
Lauren C. Chong,Susana Ben-Neriah,Graham W. Slack,Ciara L. Freeman,Daisuke Ennishi,Anja Mottok,Brett Collinge,Pau Abrisqueta,Pedro Farinha,Merrill Boyle,Barbara Meissner,Robert Kridel,Alina S. Gerrie,Diego Villa,Kerry J. Savage,Laurie H. Sehn,Reiner Siebert,Ryan D. Morin,Randy D. Gascoyne,Marco A. Marra,Joseph M. Connors,Andrew J. Mungall,Christian Steidl,David W. Scott +23 more
TL;DR: The data reveal clinically relevant architecture of MYC rearrangements in lymphomas with DLBCL morphology and shows a trend toward inferior time to progression and overall survival compared with MYC-non-IG rearrangement.
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Histopathology Reporting: Guidelines for Surgical Cancer
TL;DR: This chapter discusses Gastrointestinal Cancer, Bone and Soft Tissue Cancer, and Ophthalmic Cancer: Intraocular Malignancy.
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.
Journal ArticleDOI
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
Xose S. Puente,Magda Pinyol,Víctor Quesada,Laura Conde,Gonzalo R. Ordóñez,Neus Villamor,Geòrgia Escaramís,Pedro Jares,Sílvia Beà,Marcos González-Díaz,Laia Bassaganyas,Tycho Baumann,Manel Juan,Mónica López-Guerra,Dolors Colomer,Jose M. C. Tubio,Cristina López,Alba Navarro,Cristian Tornador,Marta Aymerich,María Rozman,Jesús M. Hernández,Diana A. Puente,José M.P. Freije,Gloria Velasco,Ana Gutiérrez-Fernández,Dolors Costa,Anna Carrió,Sara Guijarro,Anna Enjuanes,Lluis Hernández,Jordi Yagüe,Pilar Nicolás,Carlos M. Romeo-Casabona,Heinz Himmelbauer,Ester Castillo,Juliane C. Dohm,Silvia de Sanjosé,Miguel A. Piris,Enrique de Alava,Jesús F. San Miguel,Romina Royo,Josep Lluís Gelpí,David Torrents,Modesto Orozco,David G. Pisano,Alfonso Valencia,Roderic Guigó,Mònica Bayés,Simon Heath,Marta Gut,Peter Klatt,John Marshall,Keiran Raine,Lucy Stebbings,P. Andrew Futreal,Michael R. Stratton,Peter J. Campbell,Ivo Gut,Armando López-Guillermo,Xavier Estivill,Emili Montserrat,Carlos López-Otín,Elias Campo +63 more
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.
Journal ArticleDOI
MYD88 L265P Somatic Mutation in Waldenström's Macroglobulinemia
Steven P. Treon,Lian Xu,Guang Yang,Yangsheng Zhou,Xia Liu,Yang Cao,Patricia Sheehy,Robert Manning,Christopher J. Patterson,Christina K. Tripsas,Luca Arcaini,Geraldine S. Pinkus,Scott J. Rodig,Aliyah R. Sohani,Nancy L. Harris,Jason M. Laramie,Donald A Skifter,Stephen E Lincoln,Zachary R. Hunter +18 more
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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