Peripheral T-cell Lymphoma Following Diffuse Large B-cell Lymphoma Associated with Celiac Disease

Makishima, Hideki; Komiyama, Yuichi; Asano, Naoki; Momose, Kayoko; Nakamura, Shigeo; Ishida, Fumihiro

doi:10.2169/internalmedicine.47.0500

Cited by 10 publications

(7 citation statements)

References 22 publications

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“…However, intestinal T-cell lymphomas associated with celiac disease are very rare in our country. Because celiac disease is uncommon in Far East Asia [7], some characteristics of EATL in this region may differ from those in Western countries even though they have morphologic similarities. To test this hypothesis, we analyzed the clinicopathologic findings and genomic profiles of 8 Korean cases of EATL.…”

Section: Introductionmentioning

confidence: 99%

Enteropathy-associated T-cell lymphoma—a clinicopathologic and array comparative genomic hybridization study

Karnan

Kim

et al. 2010

Human Pathology

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Section: Introductionmentioning

confidence: 99%

Enteropathy-associated T-cell lymphoma—a clinicopathologic and array comparative genomic hybridization study

Karnan

Kim

et al. 2010

Human Pathology

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“…In addition to the lymphomas included in the current study, chronic lymphocytic leukemia, acute lymphoblastic leukemia, and acute myeloid leukemia have been reported being positive on [ 68 Ga]pentixafor PET [4,[11][12][13]. In vitro studies with ow cytometry, reverse transcription-polymerase chain reaction, and immunohistochemical analysis also detected strong expression of CXCR4 in hairy cell leukemia, T cell lymphoblastic lymphoma/leukemia, Sézary syndrome, angioimmunoblastic lymphoma, and anaplastic large cell lymphoma [32][33][34][35][36][37][38][39]. The CXCR4-targeted imaging with [ 68 Ga]pentixafor in these lymphoma/leukemia needs to be further investigated.…”

Section: Resultsmentioning

confidence: 55%

Preliminary evidence of imaging of chemokine receptor-4 targeted PET/CT with [68Ga]pentixafor in non-Hodgkin lymphoma: comparison to [18F]FDG

Pan

Luo

Zhang

et al. 2020

Preprint

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Background: In order to study the CXCR4 expression with [68Ga]pentixafor PET in different types of non-Hodgkin lymphoma, we performed a retrospective study to describe the [68Ga]pentixafor PET/CT imaging in a spectrum of lymphomas and to compare it with [18F]FDG PET/CT. Results: Twenty-seven patients with newly diagnosed non-Hodgkin lymphoma were recruited retrospectively. [68Ga]pentixafor PET showed increased radioactivity in lymphoplasmacytic lymphoma (n = 8), marginal zone lymphoma (n = 4), diffuse large B cell lymphoma (n = 3), follicular lymphoma (n = 2), mantle cell lymphoma (n = 1), unclassified indolent B cell lymphoma (n = 3) and enteropathy associated T cell lymphoma (n = 3). However, peripheral T cell lymphoma, not otherwise specified (n = 1), and NK/T cell lymphoma (n = 2) were not avid for [68Ga]pentixafor. In comparison to [18F]FDG PET, [68Ga]pentixafor PET demonstrated more extensive disease and higher radioactivity in lymphoplasmacytic lymphoma and marginal zone lymphoma. Conclusion: CXCR4 expression varies in different types of non-Hodgkin lymphoma. Overexpression of CXCR4 was detected with [68Ga]pentixafor PET/CT in lymphoplasmacytic lymphoma, marginal zone lymphoma, diffuse large B cell lymphoma, follicular lymphoma, mantle cell lymphoma, unclassified indolent B cell lymphoma, and enteropathy associated T cell lymphoma. The uptake of [68Ga]pentixafor was higher than [18F]FDG in lymphoplasmacytic lymphoma and marginal zone lymphoma.

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“…The five of the seven patients had malignant lymphoma, including mucosa-associated lymphoid tissue (MALT) lymphoma (n=2), diffuse large B-cell lymphoma (DLBCL) (n=1), and peripheral T-cell lymphoma, unspecified (PTCL-u) (n=1). The other presented both DLBCL and PTCL-u at different times during the 28 months of his clinical course (patient #2), which was the case reported previously 14, 15. All five cases had lymphoma lesions in the gastrointestinal tract.…”

Section: Resultsmentioning

confidence: 71%

Screening Tests Using Serum Tissue Transglutaminase IgA May Facilitate the Identification of Undiagnosed Celiac Disease among Japanese Population

Nakazawa¹,

Makishima²,

Ito³

et al. 2014

Int. J. Med. Sci.

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The prevalence of celiac disease (CD) among Japanese population has been unknown, whereas it has been increasingly recognized in the US and in the European countries. The aim of the present study is to identify possible cases with CD among Japanese population and clarify the relevance of screening for the disease.We conducted a serologic screening for the disease among 710 Japanese patients and 239 healthy volunteers at a local tertiary teaching hospital, using an anti-tissue transglutaminase IgA (TTG-IgA) test, and histological examination of the small intestines from the TTG-IgA positive subjects.There were no TTG-IgA positive sera among the healthy volunteers. Twenty of the patients (2.8%), including eight with malignant lymphoma, were tested positive for TTG-IgA. The histological examination of the eleven patients among those with positive TTG-IgA, seven showed villous atrophy and partial lymphocytes infiltration in the mucosa, which could be compatible to mucosal changes observed in CD. Five of them had non-Hodgkin lymphoma in the gastrointestinal tracts.Serologic tests using TTG-IgA might be relevant to screen for those with undiagnosed CD among Japanese population.

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Peripheral T-cell Lymphoma Following Diffuse Large B-cell Lymphoma Associated with Celiac Disease

Abstract: Abstract

Cited by 10 publications

References 22 publications

Enteropathy-associated T-cell lymphoma—a clinicopathologic and array comparative genomic hybridization study

Enteropathy-associated T-cell lymphoma—a clinicopathologic and array comparative genomic hybridization study

Preliminary evidence of imaging of chemokine receptor-4 targeted PET/CT with [68Ga]pentixafor in non-Hodgkin lymphoma: comparison to [18F]FDG

Screening Tests Using Serum Tissue Transglutaminase IgA May Facilitate the Identification of Undiagnosed Celiac Disease among Japanese Population

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