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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Main Authors: Atsunori Tsuchiya, Tomoyuki Tanaka, Yasuhiko Shibasaki, Shuji Terai
Format: Article
Language:English
Published: Wiley 2020-04-01
Series:JGH Open
Subjects:
Online Access:https://doi.org/10.1002/jgh3.12253
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spelling doaj-0a627f90effb43f3ad663e304ed81d1f2021-05-02T16:43:57ZengWileyJGH Open2397-90702020-04-014231231410.1002/jgh3.12253Hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding T‐cell lymphomaAtsunori Tsuchiya0Tomoyuki Tanaka1Yasuhiko Shibasaki2Shuji Terai3Division of Gastroenterology and Hepatology, Graduate School of Medical and Dental Sciences Niigata University Niigata JapanDepartment of Hematology, Endocrinology and Metabolism, Faculty of Medicine Niigata University Niigata JapanDepartment of Hematology, Endocrinology and Metabolism, Faculty of Medicine Niigata University Niigata JapanDivision of Gastroenterology and Hepatology, Graduate School of Medical and Dental Sciences Niigata University Niigata JapanA 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.https://doi.org/10.1002/jgh3.12253hypereosinophiliainterleukin‐5malignant lymphomamultiple liver tumorsultrasonography
collection DOAJ
language English
format Article
sources DOAJ
author Atsunori Tsuchiya
Tomoyuki Tanaka
Yasuhiko Shibasaki
Shuji Terai
spellingShingle Atsunori Tsuchiya
Tomoyuki Tanaka
Yasuhiko Shibasaki
Shuji Terai
Hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding T‐cell lymphoma
JGH Open
hypereosinophilia
interleukin‐5
malignant lymphoma
multiple liver tumors
ultrasonography
author_facet Atsunori Tsuchiya
Tomoyuki Tanaka
Yasuhiko Shibasaki
Shuji Terai
author_sort Atsunori Tsuchiya
title 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_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_sort hypereosinophilia‐related liver pseudotumor with elevated interleukin‐5 levels preceding t‐cell lymphoma
publisher Wiley
series JGH Open
issn 2397-9070
publishDate 2020-04-01
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.
topic hypereosinophilia
interleukin‐5
malignant lymphoma
multiple liver tumors
ultrasonography
url https://doi.org/10.1002/jgh3.12253
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AT tomoyukitanaka hypereosinophiliarelatedliverpseudotumorwithelevatedinterleukin5levelsprecedingtcelllymphoma
AT yasuhikoshibasaki hypereosinophiliarelatedliverpseudotumorwithelevatedinterleukin5levelsprecedingtcelllymphoma
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