2004
DOI: 10.1016/j.humpath.2004.06.001
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ALK-positive diffuse large B-cell lymphoma of the stomach associated with a clathrin-ALK rearrangement

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Cited by 38 publications
(28 citation statements)
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References 16 publications
(16 reference statements)
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“…Thus, ALK gene rearrangements, originally thought to be uniquely associated with T-/null cell ALCL, have now been convincingly shown to occur in rare cases of B-cell lymphoma. [2][3][4][5][6][7][8][9][10][11][12][13] Of note, prior to the initial series by Delsol et al, 1 Arber et al 17 in 1996 reported NPM/ALK fusion transcripts (by RT-PCR) in four of 33 cases of large B-cell lymphoma. Interestingly, and in contrast to the cases of ALK-DLBCL reported thus far, these four cases had a conventional B-cell immunophenotype (CD20 þ and CD79a þ ).…”
Section: -6mentioning
confidence: 99%
See 1 more Smart Citation
“…Thus, ALK gene rearrangements, originally thought to be uniquely associated with T-/null cell ALCL, have now been convincingly shown to occur in rare cases of B-cell lymphoma. [2][3][4][5][6][7][8][9][10][11][12][13] Of note, prior to the initial series by Delsol et al, 1 Arber et al 17 in 1996 reported NPM/ALK fusion transcripts (by RT-PCR) in four of 33 cases of large B-cell lymphoma. Interestingly, and in contrast to the cases of ALK-DLBCL reported thus far, these four cases had a conventional B-cell immunophenotype (CD20 þ and CD79a þ ).…”
Section: -6mentioning
confidence: 99%
“…1 Recently however, Clathrin/ALK (CLTC/ALK) and NPM/ALK gene rearrangements have been identified in 16 and three cases of ALK-DLBCL, respectively. [2][3][4][5][6][7][8][9][10][11][12][13] All of these cases display the morphologic and immunophenotypic features of ALK-DLBCL, as originally described by Delsol et al Importantly, ALK positivity and ALK gene rearrangements can be seen in B-cell lymphomas and are now no longer uniquely restricted to the T-cell lymphoma, ALCL. To our knowledge, only 29 cases of ALK-DLBCL have been reported thus far in the literature.…”
mentioning
confidence: 99%
“…Up to now, 15 cases of ALK þ DLBCL have been reported in literature. [41][42][43][44][45][46][47] These cases are characterized by a distinct morphology and phenotype. The tumor is composed of a diffuse, rather monotonous proliferation of large immunoblast-or plasmablast-like cells with a plasma cell phenotype (CD20À/CD79a7/CD138 þ ) and a strong submembranous granular cytoplasmic staining for ALK.…”
Section: Alk þ Dlbclmentioning
confidence: 99%
“…First, chromosomal translocation t(2;17)(p23;q23) fuses CHC17 with an intact trimerization domain (aa1-1634) to the C-terminus (aa1058-1620) of anaplastic lymphoma kinase (ALK) (40). The CHC-ALK fusion is often detected in non-Hodgkin's lymphomas and has been reported in anaplastic nul/T-cell lymphoma (41,42), large B-cell lymphoma (43)(44)(45)(46)(47)(48)(49)(50), and the rare inflammatory myofibroblastic tumor (51,52). To initiate ALKmediated lymphomagenesis, Stat3 must be activated (53).…”
Section: Oncogenic Fusionsmentioning
confidence: 99%