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Thymic inflammatory pseudotumor with multilocular thymic cyst caused by immunoglobulin G4‐related disease

A 44‐year‐old man was referred to our hospital after an anterior mediastinal tumor was noted on computed tomography during follow‐up observation after left testicular seminoma resection. Chest computed tomography revealed an enhanced mass measuring 33 x 16 x 15 mm at the anterior mediastinum. Chest...

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Autores principales: Oda, Risa, Okuda, Katsuhiro, Murase, Takayuki, Watanabe, Takuya, Sakane, Tadashi, Tatematsu, Tsutomu, Yokota, Keisuke, Haneda, Hiroshi, Nakanishi, Ryoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312835/
https://www.ncbi.nlm.nih.gov/pubmed/30467988
http://dx.doi.org/10.1111/1759-7714.12914
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author Oda, Risa
Okuda, Katsuhiro
Murase, Takayuki
Watanabe, Takuya
Sakane, Tadashi
Tatematsu, Tsutomu
Yokota, Keisuke
Haneda, Hiroshi
Nakanishi, Ryoichi
author_facet Oda, Risa
Okuda, Katsuhiro
Murase, Takayuki
Watanabe, Takuya
Sakane, Tadashi
Tatematsu, Tsutomu
Yokota, Keisuke
Haneda, Hiroshi
Nakanishi, Ryoichi
author_sort Oda, Risa
collection PubMed
description A 44‐year‐old man was referred to our hospital after an anterior mediastinal tumor was noted on computed tomography during follow‐up observation after left testicular seminoma resection. Chest computed tomography revealed an enhanced mass measuring 33 x 16 x 15 mm at the anterior mediastinum. Chest magnetic resonance imaging revealed high signal intensity on T2‐weighted imaging, and F(18) fluorodeoxyglucose‐positron emission tomography showed a maximum standardized uptake of 12.45. Laboratory tests revealed no elevated tumor markers, except for mildly elevated interleukin‐2. Based on these results, complete resection was performed under suspicion of a malignant tumor, mediastinal metastasis of seminoma, or malignant lymphoma. An extended thymectomy with partial merger pericardial resection was performed using a subxiphoid approach. Small nodules and multiple thymic cysts were observed the thymus in addition to the main mass. Microscopic examination of the tumor revealed fibrosis, lymphocyte infiltration with lymphoid follicular hyperplasia, and hyperplasia of the thymus. Numerous immunoglobulin G4 (IgG4)‐positive plasma cells were found on immunohistochemical staining. The ratio of IgG4 to total IgG was approximately 60%. We ultimately diagnosed the patient with a thymic inflammatory pseudotumor with multilocular cyst caused by IgG4‐related disease.
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spelling pubmed-63128352019-01-07 Thymic inflammatory pseudotumor with multilocular thymic cyst caused by immunoglobulin G4‐related disease Oda, Risa Okuda, Katsuhiro Murase, Takayuki Watanabe, Takuya Sakane, Tadashi Tatematsu, Tsutomu Yokota, Keisuke Haneda, Hiroshi Nakanishi, Ryoichi Thorac Cancer Case Reports A 44‐year‐old man was referred to our hospital after an anterior mediastinal tumor was noted on computed tomography during follow‐up observation after left testicular seminoma resection. Chest computed tomography revealed an enhanced mass measuring 33 x 16 x 15 mm at the anterior mediastinum. Chest magnetic resonance imaging revealed high signal intensity on T2‐weighted imaging, and F(18) fluorodeoxyglucose‐positron emission tomography showed a maximum standardized uptake of 12.45. Laboratory tests revealed no elevated tumor markers, except for mildly elevated interleukin‐2. Based on these results, complete resection was performed under suspicion of a malignant tumor, mediastinal metastasis of seminoma, or malignant lymphoma. An extended thymectomy with partial merger pericardial resection was performed using a subxiphoid approach. Small nodules and multiple thymic cysts were observed the thymus in addition to the main mass. Microscopic examination of the tumor revealed fibrosis, lymphocyte infiltration with lymphoid follicular hyperplasia, and hyperplasia of the thymus. Numerous immunoglobulin G4 (IgG4)‐positive plasma cells were found on immunohistochemical staining. The ratio of IgG4 to total IgG was approximately 60%. We ultimately diagnosed the patient with a thymic inflammatory pseudotumor with multilocular cyst caused by IgG4‐related disease. John Wiley & Sons Australia, Ltd 2018-11-23 2019-01 /pmc/articles/PMC6312835/ /pubmed/30467988 http://dx.doi.org/10.1111/1759-7714.12914 Text en © 2018 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Oda, Risa
Okuda, Katsuhiro
Murase, Takayuki
Watanabe, Takuya
Sakane, Tadashi
Tatematsu, Tsutomu
Yokota, Keisuke
Haneda, Hiroshi
Nakanishi, Ryoichi
Thymic inflammatory pseudotumor with multilocular thymic cyst caused by immunoglobulin G4‐related disease
title Thymic inflammatory pseudotumor with multilocular thymic cyst caused by immunoglobulin G4‐related disease
title_full Thymic inflammatory pseudotumor with multilocular thymic cyst caused by immunoglobulin G4‐related disease
title_fullStr Thymic inflammatory pseudotumor with multilocular thymic cyst caused by immunoglobulin G4‐related disease
title_full_unstemmed Thymic inflammatory pseudotumor with multilocular thymic cyst caused by immunoglobulin G4‐related disease
title_short Thymic inflammatory pseudotumor with multilocular thymic cyst caused by immunoglobulin G4‐related disease
title_sort thymic inflammatory pseudotumor with multilocular thymic cyst caused by immunoglobulin g4‐related disease
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312835/
https://www.ncbi.nlm.nih.gov/pubmed/30467988
http://dx.doi.org/10.1111/1759-7714.12914
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