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
Citations
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Characterization of the fecal microbiome in cats with inflammatory bowel disease or alimentary small cell lymphoma.
Sina Marsilio,Sina Marsilio,Rachel Pilla,Benjamin Sarawichitr,Betty Chow,Steve Hill,Mark R. Ackermann,J. Scot Estep,Jonathan A. Lidbury,Joerg M. Steiner,Jan S. Suchodolski +10 more
TL;DR: Feline chronic enteropathy in cats showed patterns of dysbiosis similar to those in found people with IBD, and no significant difference between the microbiome of cats with I BD and those with SCL was found.
Journal ArticleDOI
Follicular lymphoma t(14;18)-negative is genetically a heterogeneous disease
Dominik Nann,Joan Enric Ramis-Zaldivar,Inga Müller,Blanca Gonzalez-Farre,Janine Schmidt,Caoimhe Egan,Julia Salmeron-Villalobos,Guillem Clot,Sven Mattern,Franziska Otto,Barbara Mankel,Dolors Colomer,Olga Balagué,Vanessa Szablewski,Carmen Lome-Maldonado,Lorenzo Leoncini,Stefan Dojcinov,Andreas Chott,Christiane Copie-Bergman,Irina Bonzheim,Falko Fend,Elaine S. Jaffe,Elias Campo,Itziar Salaverria,Leticia Quintanilla-Martinez +24 more
TL;DR: Overall, t(14;18)- FL is genetically a heterogeneous disorder with features that differ from cFL, NMZL, and PTFL, and a positive correlation with CD23 expression.
Journal ArticleDOI
CD79B mutations in primary vitreoretinal lymphoma: Diagnostic and prognostic potential.
Ichiro Yonese,Hiroshi Takase,Mayumi Yoshimori,Erika Onozawa,Akiho Tsuzura,Tohru Miki,Manabu Mochizuki,Osamu Miura,Ayako Arai +8 more
TL;DR: The mutation in PVRL was examined to clarify its diagnostic and prognostic potential and to clarify the development of central nervous system (CNS) lesions during its course.
Journal ArticleDOI
A distinct subtype of Epstein-Barr virus-positive T/NK-cell lymphoproliferative disorder: adult patients with chronic active Epstein-Barr virus infection-like features.
Keisuke Kawamoto,Hiroaki Miyoshi,Takaharu Suzuki,Yasuji Kozai,Koji Kato,Masaharu Miyahara,Toshiaki Yujiri,Ilseung Choi,Katsumichi Fujimaki,Tsuyoshi Muta,Masaaki Kume,Sayaka Moriguchi,Shinobu Tamura,Takeharu Kato,Hiroyuki Tagawa,Junya Makiyama,Yuji Kanisawa,Yuya Sasaki,Daisuke Kurita,Kyohei Yamada,Joji Shimono,Hirohito Sone,Jun Takizawa,Masao Seto,Hiroshi Kimura,Koichi Ohshima +25 more
TL;DR: Adult-onset chronic active Epstein-Barr virus infection is a disease with a poor prognosis, and patients with nasal-type and non-nasal-type extranodal NK/T-cell lymphoma have a poorer prognosis.
Journal ArticleDOI
EBV-associated primary CNS lymphoma occurring after immunosuppression is a distinct immunobiological entity
Maher K. Gandhi,Maher K. Gandhi,Thanh Hoang,Soi Cheng Law,Sandra Brosda,K. O’Rourke,Joshua W.D. Tobin,Frank Vari,Valentine Murigneux,Lynn Fink,Jay Gunawardana,Clare Gould,Harald Oey,Karolina Bednarska,S. Delecluse,Ralf Ulrich Trappe,L. Merida de Long,Muhammed B. Sabdia,Govind Bhagat,Greg Hapgood,Emily Blyth,Leighton Clancy,Joel Wight,Eliza A Hawkes,Lisa M. Rimsza,Alanna Maguire,Kamil Bojarczuk,Björn Chapuy,Colm Keane,Colm Keane +29 more
TL;DR: EBV-tissue positive PCNSL in the immunosuppressed is immunobiologically distinct from EBV(-) HIV(-) PCNSl, and despite expressing an immunogenic virus retains the ability to present EBV-antigens.
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.
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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