Literature DB >> 21423155

Primary intestinal T-cell and NK-cell lymphomas: a clinicopathological and molecular study from China focused on type II enteropathy-associated T-cell lymphoma and primary intestinal NK-cell lymphoma.

Jian Sun1, Zhaohui Lu, Di Yang, Jie Chen.   

Abstract

In China, which is a non-endemic area for celiac disease, primary intestinal T-cell and NK-cell lymphomas might comprise heterogeneous subtypes. Both type II enteropathy-associated T-cell lymphoma and primary intestinal NK-cell lymphoma are rarely reported and poorly characterized in China. In this study, we examined the clinicopathological and molecular features of 38 cases of primary intestinal T-cell and NK-cell lymphoma in Chinese patients. Based on these findings, we first classified the patients into an NK-cell group (n=6) and a T-cell group (n=32). In the NK-cell group, the mean age was 37 years. All tumors of the NK-cell group were positive for Epstein-Barr virus encoded mRNA in the majority of tumor cells and were polyclonal according to the results of commercial BIOMED-2 T-cell receptor gene rearrangement assays. The survival in the NK-cell group was significantly worse than that of the T-cell group (P=0.0247). Next, 7 tumors of the T-cell group were considered type II enteropathy-associated T-cell lymphoma, while 24 were considered peripheral T-cell lymphoma, not otherwise specified (NOS). In the type II enteropathy-associated T-cell lymphoma group, the mean age was 55 years. Type II enteropathy-associated T-cell lymphoma tumor cells from all seven patients were monomorphic, medium sized. The survival in the type II enteropathy-associated T-cell lymphoma group was significantly worse than that of the peripheral T-cell lymphoma, NOS group (P=0.0181). Multivariate analysis identified NK-cell phenotype, male gender, and CD8 positivity as factors for poor prognosis in our series of primary intestinal T-cell and NK-cell lymphoma patients. In conclusion, most cases of primary intestinal T-cell and NK-cell lymphoma in China are not associated with celiac disease and could be classified to NK-cell group, type II enteropathy-associated T-cell lymphoma group, and peripheral T-cell lymphoma, NOS group. Each group has distinctive histopathological features with prognostic significance.

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Year:  2011        PMID: 21423155     DOI: 10.1038/modpathol.2011.45

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  21 in total

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Journal:  World J Gastroenterol       Date:  2014-01-07       Impact factor: 5.742

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Review 7.  Enteropathy-Associated T-Cell Lymphoma.

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Journal:  Curr Hematol Malig Rep       Date:  2016-12       Impact factor: 3.952

8.  Clinically undiagnosed enteropathy associated T-cell lymphoma type II presenting with prolonged lower gastrointestinal tract symptoms: report of an autopsy case and review of diagnostic challenges and clinicopathological correlation.

Authors:  Andrew J Rand; Diana M Cardona; Alan D Proia; Anand S Lagoo
Journal:  J Gastrointest Oncol       Date:  2013-03

9.  Primary intestinal extranodal natural killer/T-cell lymphoma, nasal type: A case report.

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Journal:  World J Clin Cases       Date:  2020-01-06       Impact factor: 1.337

10.  Perforation of the small intestine caused by enteropathy-associated T cell lymphoma.

Authors:  Selva Kabul; Nesrin Uğraş; Ömer Yerci; Ersin Öztürk
Journal:  Turk J Surg       Date:  2018-01-03
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