Monomorphic epitheliotropic intestinal T-cell lymphoma comprises morphologic and genomic heterogeneity impacting outcome

Autor: Luis Veloza, Doriane Cavalieri, Edoardo Missiaglia, Albane Ledoux-Pilon, Bettina Bisig, Bruno Pereira, Christophe Bonnet, Elsa Poullot, Leticia Quintanilla-Martinez, Romain Dubois, Francisco Llamas-Gutierrez, Céline Bossard, Roland De Wind, Fanny Drieux, Juliette Fontaine, Marie Parrens, Jeremy Sandrini, Virginie Fataccioli, Marie-Hélène Delfau-Larue, Adrien Daniel, Faustine Lhomme, Lauriane Clément-Filliatre, François Lemonnier, Anne Cairoli, Pierre Morel, Sylvie Glaisner, Bertrand Joly, Abderrazak El Yamani, Kamel Laribi, Emmanuel Bachy, Reiner Siebert, David Vallois, Philippe Gaulard, Olivier Tournilhac, Laurence De Leval

Publikováno v: Haematologica, vol. 108, no. 1, pp. 181-195

Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) is a rare aggressive T-cell lymphoma most reported in Asia. We performed a comprehensive clinical, pathological and genomic study of 71 European MEITL patients (36 males, 35 females, medi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c84ad149728e38912551fdf7d669d17
https://doi.org/10.3324/haematol.2022.281226

The International Consensus Classification of Mature Lymphoid Neoplasms: a report from the Clinical Advisory Committee

Autor: Campo, E., Jaffe, E.S., Cook, J.R., Quintanilla-Martinez, L., Swerdlow, S.H., Anderson, K.C., Brousset, P., Cerroni, L., de Leval, L., Dirnhofer, S., Dogan, A., Feldman, A.L., Fend, F., Friedberg, J.W., Gaulard, P., Ghia, P., Horwitz, S.M., King, R.L., Salles, G., San-Miguel, J., Seymour, J.F., Treon, S.P., Vose, J.M., Zucca, E., Advani, R., Ansell, S., Au, W.Y., Barrionuevo, C., Bergsagel, L., Chan, W.C., Cohen, J.I., d'Amore, F., Davies, A., Falini, B., Ghobrial, I.M., Goodlad, J.R., Gribben, J.G., Hsi, E.D., Kahl, B.S., Kim, W.S., Kumar, S., LaCasce, A.S., Laurent, C., Lenz, G., Leonard, J.P., Link, M.P., Lopez-Guillermo, A., Mateos, M.V., Macintyre, E., Melnick, A.M., Morschhauser, F., Nakamura, S., Narbaitz, M., Pavlovsky, A., Pileri, S.A., Piris, M., Pro, B., Rajkumar, V., Rosen, S.T., Sander, B., Sehn, L., Shipp, M.A., Smith, S.M., Staudt, L.M., Thieblemont, C., Tousseyn, T., Wilson, W.H., Yoshino, T., Zinzani, P.L., Dreyling, M., Scott, D.W., Winter, J.N., Zelenetz, A.D.

Publikováno v: Blood, vol. 140, no. 11, pp. 1229-1253

Since the publication of the Revised European-American Classification of Lymphoid Neoplasms in 1994, subsequent updates of the classification of lymphoid neoplasms have been generated through iterative international efforts to achieve broad consensus

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1900::9d6d6db77ed0140f6fbe09a0a2f5e110
https://serval.unil.ch/notice/serval:BIB_42E7F7A0538F

Life threatening rare lymphomas presenting as longitudinally extensive transverse myelitis: a diagnostic challenge

Autor: Judit Csomor, Árpád Vadvári, Zsolt Illes, Zsuzsanna Nagy, Katalin Hahn, Balázs Tolvaj, Ferenc Garzuly, Ellen Gelpi

Publikováno v: Tolvaj, B, Hahn, K, Nagy, Z, Vadvári, Á, Csomor, J, Gelpi, E, Illes, Z & Garzuly, F 2020, ' Life threatening rare lymphomas presenting as longitudinally extensive transverse myelitis : a diagnostic challenge ', Clinical Neuroscience, vol. 73, no. 7-8, pp. 275-285 . https://doi.org/10.18071/isz.73.0275

Background and aims - Description of two cases of rare intravascular large B-cell lymphoma and secondary T-cell lymphoma diagnosed postmortem, that manifested clinically as longitudinally extensive transverse myelitis (LETM). We discuss causes of dia

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93040191db640c914e88f0e1ee38edd2
https://doi.org/10.18071/isz.73.0275

Primary bone lymphoma: pictorial essay

Autor: Stefanini, Flavio Scavone, Gois, Franklin Wilson Caires, de Arruda, Tiago Cesar Silva Borba, Bitencourt, Almir Galvão Vieira, Cerqueira, Wagner Santana

Publikováno v: Radiologia Brasileira v.53 n.6 2020
Radiologia Brasileira
Colégio Brasileiro de Radiologia e Diagnóstico por Imagem (CBR)
instacron:CBR
Radiologia Brasileira, Volume: 53, Issue: 6, Pages: 419-423, Published: 20 NOV 2020
Radiologia Brasileira, Vol 53, Iss 6, Pp 419-423 (2020)

Primary bone lymphoma is a rare neoplasm that can initially present as local pain, a palpable mass, and pathologic fracture. It can also be discovered as an incidental finding on an imaging examination. It is defined as a bone marrow tumor with no in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf0829cf921753d64c036722fe9fa074
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-39842020000600419

NKp46 is a diagnostic biomarker and may be a therapeutic target in gastrointestinal T-cell lymphoproliferative diseases: A CELAC study

Autor: Nicolas Guegan, Florence Lhospice, Sascha Cording, Amélie Trinquand, Julie Bruneau, Olivier Hermine, Virginie Verkarre, Nicole Brousse, Christophe Cellier, Georgia Malamut, Elizabeth Macintyre, Felipe Suarez, Laurent Frenzel, Vahid Asnafi, Morgane Cheminant, Sherine Khater, Bertrand Meresse, Ambroise Marçais, Nadine Cerf-Bensussan, Tom van Gils, Chris J. J. Mulder, Thierry Jo Molina, Ludovic Lhermitte, C. cile Bonnafous, David Sibon, Anne-Sophie Jannot, Richard Delarue, Laurent Pouyet

Publikováno v: Gut, 68(8), 1396-1405. BMJ Publishing Group
Gut
Gut, BMJ Publishing Group, 2019, 68 (8), pp.1396-1405. ⟨10.1136/gutjnl-2018-317371⟩
Cheminant, M, Bruneau, J, Malamut, G, Sibon, D, Guegan, N, van Gils, T, Cording, S, Trinquand, A, Verkarre, V, Lhermitte, L, Brousse, N, Jannot, A-S, Khater, S, Frenzel, L, Delarue, R, Suarez, F, Marçais, A, Mulder, C J J, Macintyre, E, Asnafi, V, Pouyet, L, Bonnafous, C C, Lhospice, F, Molina, T J, Meresse, B, Cellier, C, Cerf-Bensussan, N & Hermine, O 2019, ' NKp46 is a diagnostic biomarker and may be a therapeutic target in gastrointestinal T-cell lymphoproliferative diseases: A CELAC study ', Gut, vol. 68, no. 8, pp. 1396-1405 . https://doi.org/10.1136/gutjnl-2018-317371
Gut, 2019, 68 (8), pp.1396-1405. ⟨10.1136/gutjnl-2018-317371⟩

ObjectivesPrimary GI T-cell lymphoproliferative diseases (T-LPD) are heterogeneous entities, which raise difficult diagnosis and therapeutic challenges. We have recently provided evidences that lymphomas complicating coeliac disease (CD) arise from i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70bf16bc8e37754465b0cd121bf54c22
https://research.vumc.nl/en/publications/c070e3fd-4cc5-486e-8710-e1f8ba369480