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Plasmablastic lymphoma occurring in ulcerative colitis during treatment with immunosuppressive therapy
A 53-year-old man who had a history of ulcerative colitis (UC) for 2 years underwent colonoscopy as regular follow-up. The results showed an elevated lesion in the descending colon, which was diagnosed as plasmablastic lymphoma (PBL) based on pathological findings. In situ hybridization for the Epst...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Nature Singapore
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821367/ https://www.ncbi.nlm.nih.gov/pubmed/36609818 http://dx.doi.org/10.1007/s12328-023-01754-5 |
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author | Ogiyama, Hideharu Murayama, Yoko Tsutsui, Shusaku Iwasaki, Tetsuya Kuriyama, Daisuke Horiki, Masashi Imanaka, Kazuho Kimura, Hayato Inoue, Megumu Iishi, Hiroyasu |
author_facet | Ogiyama, Hideharu Murayama, Yoko Tsutsui, Shusaku Iwasaki, Tetsuya Kuriyama, Daisuke Horiki, Masashi Imanaka, Kazuho Kimura, Hayato Inoue, Megumu Iishi, Hiroyasu |
author_sort | Ogiyama, Hideharu |
collection | PubMed |
description | A 53-year-old man who had a history of ulcerative colitis (UC) for 2 years underwent colonoscopy as regular follow-up. The results showed an elevated lesion in the descending colon, which was diagnosed as plasmablastic lymphoma (PBL) based on pathological findings. In situ hybridization for the Epstein–Barr virus-encoded RNA probe was positive. Fluorescence in situ hybridization revealed rearrangement of the MYC gene. He had been taking prednisolone, 5-aminosalicylic acid, azathiopurine, and ustekinumab at the diagnosis of PBL and had multiple prior therapies for UC including infliximab, tacrolimus, and tofacitinib due to steroid dependence. PBL is a rare aggressive B cell lymphoma initially described in the oral cavity of human immunodeficiency virus positive patients and it is suspected to have an association with immunocompromised status of patients. The number of cases of PBL in inflammatory bowel disease (IBD) patients is extremely rare. All these patients were administered immunosuppressive therapy including thiopurines or biologics. IBD patients with immunosuppressive therapy have a higher potential for developing lymphoproliferative disorders. Clinicians should be aware of the risk of lymphoma, including PBL. |
format | Online Article Text |
id | pubmed-9821367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-98213672023-01-09 Plasmablastic lymphoma occurring in ulcerative colitis during treatment with immunosuppressive therapy Ogiyama, Hideharu Murayama, Yoko Tsutsui, Shusaku Iwasaki, Tetsuya Kuriyama, Daisuke Horiki, Masashi Imanaka, Kazuho Kimura, Hayato Inoue, Megumu Iishi, Hiroyasu Clin J Gastroenterol Case Report A 53-year-old man who had a history of ulcerative colitis (UC) for 2 years underwent colonoscopy as regular follow-up. The results showed an elevated lesion in the descending colon, which was diagnosed as plasmablastic lymphoma (PBL) based on pathological findings. In situ hybridization for the Epstein–Barr virus-encoded RNA probe was positive. Fluorescence in situ hybridization revealed rearrangement of the MYC gene. He had been taking prednisolone, 5-aminosalicylic acid, azathiopurine, and ustekinumab at the diagnosis of PBL and had multiple prior therapies for UC including infliximab, tacrolimus, and tofacitinib due to steroid dependence. PBL is a rare aggressive B cell lymphoma initially described in the oral cavity of human immunodeficiency virus positive patients and it is suspected to have an association with immunocompromised status of patients. The number of cases of PBL in inflammatory bowel disease (IBD) patients is extremely rare. All these patients were administered immunosuppressive therapy including thiopurines or biologics. IBD patients with immunosuppressive therapy have a higher potential for developing lymphoproliferative disorders. Clinicians should be aware of the risk of lymphoma, including PBL. Springer Nature Singapore 2023-01-06 2023 /pmc/articles/PMC9821367/ /pubmed/36609818 http://dx.doi.org/10.1007/s12328-023-01754-5 Text en © Japanese Society of Gastroenterology 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Case Report Ogiyama, Hideharu Murayama, Yoko Tsutsui, Shusaku Iwasaki, Tetsuya Kuriyama, Daisuke Horiki, Masashi Imanaka, Kazuho Kimura, Hayato Inoue, Megumu Iishi, Hiroyasu Plasmablastic lymphoma occurring in ulcerative colitis during treatment with immunosuppressive therapy |
title | Plasmablastic lymphoma occurring in ulcerative colitis during treatment with immunosuppressive therapy |
title_full | Plasmablastic lymphoma occurring in ulcerative colitis during treatment with immunosuppressive therapy |
title_fullStr | Plasmablastic lymphoma occurring in ulcerative colitis during treatment with immunosuppressive therapy |
title_full_unstemmed | Plasmablastic lymphoma occurring in ulcerative colitis during treatment with immunosuppressive therapy |
title_short | Plasmablastic lymphoma occurring in ulcerative colitis during treatment with immunosuppressive therapy |
title_sort | plasmablastic lymphoma occurring in ulcerative colitis during treatment with immunosuppressive therapy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821367/ https://www.ncbi.nlm.nih.gov/pubmed/36609818 http://dx.doi.org/10.1007/s12328-023-01754-5 |
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