Literature DB >> 16625103

Atypical NK-cell proliferation of the gastrointestinal tract in a patient with antigliadin antibodies but not celiac disease.

Francisco Vega1, Chung-Che Chang, Mary R Schwartz, Hector Alejandro Preti, Mamoun Younes, April Ewton, Ray Verm, Elaine S Jaffe.   

Abstract

We describe a unique case of atypical natural killer (NK)-cell proliferation likely related to gluten sensitivity, mimicking NK-cell lymphoma. The patient, a 32-year-old man, has had persistent multiple erythematous bull-eye lesions in the stomach, small bowel, and large bowel for 3 years. Histologically, the lesions were well circumscribed and relatively superficial, composed of atypical medium-sized to large-sized lymphocytes with slightly irregular nuclear contours, a dispersed chromatin pattern, and clear cytoplasm. Immunohistochemistry and flow cytometry showed that the cells were NK cells expressing CD56 (aberrantly bright), T-cell intracellular antigen (TIA)-1, cytoplasmic CD3, and CD94, but not surface CD3, with bright aberrant expression of CD7 and a lack of other NK cell-associated markers. Polymerase chain reaction for rearrangement of the T-cell receptor-gamma chain gene showed no evidence of a clonal T-cell population, and in situ hybridization for Epstein-Barr virus encoded RNA was negative. There was no evidence of the involvement of peripheral blood or bone marrow. Although a diagnosis of extranodal NK/T-cell lymphoma was considered because of the atypical morphology and immunophenotypic aberrancy, no chemotherapy was given because of the relatively superficial nature of the infiltrates, lack of significant symptoms, and negativity for Epstein-Barr virus. Two years after initial presentation, the patient was found to have high titers of antigliadin antibodies with no other evidence of celiac disease. After instituting a gluten-free diet, many of the lesions regressed, suggesting that this atypical NK-cell proliferation may be driven by an anomalous immune response. Awareness of this case may prevent pathologists from misdiagnosing similar lesions as NK/T-cell lymphomas. It is as yet unknown whether this process occurs more commonly in patients with gluten sensitivity, or in other settings, and the pathogenesis is as yet undetermined.

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Year:  2006        PMID: 16625103     DOI: 10.1097/00000478-200604000-00017

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  9 in total

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Authors:  Karthik A Ganapathi; Stefania Pittaluga; Oreofe O Odejide; Arnold S Freedman; Elaine S Jaffe
Journal:  Haematologica       Date:  2014-09       Impact factor: 9.941

3.  Recurrent somatic JAK3 mutations in NK-cell enteropathy.

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Journal:  Blood       Date:  2019-08-05       Impact factor: 22.113

4.  NK-cell enteropathy: a benign NK-cell lymphoproliferative disease mimicking intestinal lymphoma: clinicopathologic features and follow-up in a unique case series.

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Review 5.  Cellular Origins and Pathogenesis of Gastrointestinal NK- and T-Cell Lymphoproliferative Disorders.

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Review 6.  The Microscope as a Tool for Disease Discovery-A Personal Voyage.

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Journal:  Annu Rev Pathol       Date:  2016-12-05       Impact factor: 23.472

7.  An Enteropathy-like Indolent NK-Cell Proliferation Presenting in the Female Genital Tract.

Authors:  Rahul Krishnan; Kari Ring; Eli Williams; Craig Portell; Elaine S Jaffe; Alejandro A Gru
Journal:  Am J Surg Pathol       Date:  2020-04       Impact factor: 6.298

8.  Lymphomatoid gastropathy/NK-cell enteropathy involving the stomach and intestine.

Authors:  Makoto Nakajima; Masayuki Shimoda; Kengo Takeuchi; Akito Dobashi; Takanori Kanai; Yae Kanai; Yasushi Iwao
Journal:  J Clin Exp Hematop       Date:  2022-04-27

9.  Lymph node involvement by enteropathy-like indolent NK-cell proliferation.

Authors:  Jean-Louis Dargent; Nicolas Tinton; Mounir Trimech; Laurence de Leval
Journal:  Virchows Arch       Date:  2020-07-21       Impact factor: 4.064

  9 in total

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