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Hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding T‐cell lymphoma

A 61‐year‐old woman with hypereosinophilia and elevated interleukin (IL)‐5 level was admitted to our hospital after detection of multiple liver tumors. Liver biopsy demonstrated that the tumor consisted of scar tissue with remnants of eosinophilic infiltration, suggesting that it had formed by massi...

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Detalles Bibliográficos
Autores principales: Tsuchiya, Atsunori, Tanaka, Tomoyuki, Shibasaki, Yasuhiko, Terai, Shuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144778/
https://www.ncbi.nlm.nih.gov/pubmed/32280790
http://dx.doi.org/10.1002/jgh3.12253
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author Tsuchiya, Atsunori
Tanaka, Tomoyuki
Shibasaki, Yasuhiko
Terai, Shuji
author_facet Tsuchiya, Atsunori
Tanaka, Tomoyuki
Shibasaki, Yasuhiko
Terai, Shuji
author_sort Tsuchiya, Atsunori
collection PubMed
description A 61‐year‐old woman with hypereosinophilia and elevated interleukin (IL)‐5 level was admitted to our hospital after detection of multiple liver tumors. Liver biopsy demonstrated that the tumor consisted of scar tissue with remnants of eosinophilic infiltration, suggesting that it had formed by massive eosinophilic infiltration. The hypereosinophilia was treated mainly by prednisolone, and thereafter, the liver tumors disappeared. However, 10 months postadmission, CD4+ T‐cell lymphoma, which can produce IL‐5, was detected in the nasopharynx and oropharynx. Therefore, we believe that this is a rare case of hypereosinophilia‐related liver pseudotumor induced by presumed by IL‐5 elevation.
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spelling pubmed-71447782020-04-10 Hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding T‐cell lymphoma Tsuchiya, Atsunori Tanaka, Tomoyuki Shibasaki, Yasuhiko Terai, Shuji JGH Open Case Reports A 61‐year‐old woman with hypereosinophilia and elevated interleukin (IL)‐5 level was admitted to our hospital after detection of multiple liver tumors. Liver biopsy demonstrated that the tumor consisted of scar tissue with remnants of eosinophilic infiltration, suggesting that it had formed by massive eosinophilic infiltration. The hypereosinophilia was treated mainly by prednisolone, and thereafter, the liver tumors disappeared. However, 10 months postadmission, CD4+ T‐cell lymphoma, which can produce IL‐5, was detected in the nasopharynx and oropharynx. Therefore, we believe that this is a rare case of hypereosinophilia‐related liver pseudotumor induced by presumed by IL‐5 elevation. Wiley Publishing Asia Pty Ltd 2019-09-06 /pmc/articles/PMC7144778/ /pubmed/32280790 http://dx.doi.org/10.1002/jgh3.12253 Text en © 2019 The Authors. JGH Open: An open access journal of gastroenterology and hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Tsuchiya, Atsunori
Tanaka, Tomoyuki
Shibasaki, Yasuhiko
Terai, Shuji
Hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding T‐cell lymphoma
title Hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding T‐cell lymphoma
title_full Hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding T‐cell lymphoma
title_fullStr Hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding T‐cell lymphoma
title_full_unstemmed Hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding T‐cell lymphoma
title_short Hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding T‐cell lymphoma
title_sort hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding t‐cell lymphoma
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144778/
https://www.ncbi.nlm.nih.gov/pubmed/32280790
http://dx.doi.org/10.1002/jgh3.12253
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