Abstract

In this paper, we introduce a simplified, one-step procedure for lymphocyte isolation from an endoscopically biopsied fragment. For lymphocyte isolation, an endoscopically harvested specimen and 5 mL of normal saline solution were placed in a wire mesh strainer set in a porcelain bowl. To obtain the lymphocyte suspension, the solid specimen was crushed using the rubber portion of a plunger of a 10 mL injection syringe. Flow cytometry was performed using the lymphocyte suspension. For validating our methods, the one-step lymphocyte isolation technique was used to perform flow cytometry on samples from 23 patients with (n = 12) or without (n = 11) gastrointestinal lymphoma. Flow cytometry of light chain expression was performed in all patient samples (feasibility: 100%). Sensitivity was 83.3% (10/12) and specificity was 100% (11/11). In conclusion, lymphocytes isolated from a single endoscopic biopsy specimen using our simplified and quick procedure are suitable for flow cytometry. Considering that flow cytometry has an important advantage of providing the results on the examination day itself, the results of this study suggest that flow cytometric analysis using our single-step lymphocyte isolation technique can be potentially used to diagnose lymphoma in the gastrointestinal mucosa.•We introduce a simplified, one-step procedure for lymphocyte isolation from an endoscopically biopsied fragment.•Our technique is feasible for flow cytometric analysis in patients with gastrointestinal lymphoma as well as those with gastrointestinal lesions that are suspected to be lymphoma.

Highlights

  • Method ArticleMasaya Iwamuro a,∗, Takahide Takahashi b, Natsuki Watanabe b, Sizuma Omote c, Katsunori Matsueda d, Takehiro Tanaka c, Daisuke Ennishi e, Fumio Otsuka f, Tadashi Yoshino c, Hiroyuki Okada a a Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan b Division of Medical Support, Okayama University Hospital, Okayama 700-8558, Japan c Department of Pathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan d Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka 541-8567, Japan e Department of Hematology and Oncology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan f Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan abstract

  • We reported that flow cytometric analysis of light chain expression in endoscopic biopsy specimens was feasible for the diagnosis of gastrointestinal B-cell lymphoma using two endoscopic biopsy fragments or even a single endoscopic biopsy fragment [6,7]

  • Benign lesions consisted of lymphoid hyperplasia, eosinophilic gastritis (n = 1), erosive gastritis (n = 1), gastric cancer (n = 1), non-specific ileitis (n = 1), ulcerative colitis (n = 1), colon cancer (n = 1), and the remission stage of lymphoma

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Summary

Method Article

Masaya Iwamuro a,∗, Takahide Takahashi b, Natsuki Watanabe b, Sizuma Omote c, Katsunori Matsueda d, Takehiro Tanaka c, Daisuke Ennishi e, Fumio Otsuka f, Tadashi Yoshino c, Hiroyuki Okada a a Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan b Division of Medical Support, Okayama University Hospital, Okayama 700-8558, Japan c Department of Pathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan d Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka 541-8567, Japan e Department of Hematology and Oncology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan f Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan abstract.

Method details
Method validation
Results
Conclusion

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