Papers

International journal
Sep 11, 2019

Feasibility of flow cytometric analysis of restricted light chain in endoscopic biopsy specimens from patients with gastrointestinal tract B cell lymphoma: a pilot study.

BMC research notes
  • Katsunori Matsueda
  • ,
  • Masaya Iwamuro
  • ,
  • Takahide Takahashi
  • ,
  • Sizuma Omote
  • ,
  • Kenji Nishida
  • ,
  • Takehiro Tanaka
  • ,
  • Daisuke Ennishi
  • ,
  • Fumio Otsuka
  • ,
  • Tadashi Yoshino
  • ,
  • Hiroyuki Okada

Volume
12
Number
1
First page
571
Last page
571
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1186/s13104-019-4578-4

OBJECTIVE: Gastrointestinal tract lymphomas are currently detected more frequently due to advances in endoscopic technology. The aim of this study was to assess the feasibility of flow cytometric analysis of restricted light chain in endoscopic biopsy specimens for the diagnosis of gastrointestinal tract B-cell lymphoma. We prepared viable cell suspensions from unfixed specimens obtained from 10 consecutive patients who had a previous histological diagnosis of gastrointestinal tract B-cell lymphoma. We performed immunophenotypic studies with multi-color flow cytometry and assessed clonality through examination of immunoglobulin light chain expression exclusively in a population identified by anti-CD45 or CD20 antibodies. RESULTS: We could perform light chain expression analysis with 2 endoscopic biopsy specimens from all 10 patients with gastrointestinal tract B-cell lymphoma. We conclude that flow cytometric analysis of endoscopic biopsy specimens is feasible and thus likely useful for the diagnosis of gastrointestinal tract B-cell lymphoma in clinical settings. Trial registration UMIN Clinical Trials Registry, UMIN000027730. Registered 12 June 2017.

Link information
DOI
https://doi.org/10.1186/s13104-019-4578-4
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31511043
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737588
ID information
  • DOI : 10.1186/s13104-019-4578-4
  • Pubmed ID : 31511043
  • Pubmed Central ID : PMC6737588

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