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Sarcoidosis-Lymphoma Syndrome Associated With Primary Thyroid Lymphoma: A Case Report
Background: Sarcoidosis is occasionally accompanied by hematologic malignancies, including lymphoma, called sarcoidosis-lymphoma syndrome. Although the mechanism underlying the induction of lymphomas is still unknown, understanding the immunological background of sarcoidosis could help explain the p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089818/ http://dx.doi.org/10.1210/jendso/bvab048.1837 |
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author | Yamashita, Saori Matsuda, Yayoi Muta, Hiroki Nagao, Toshihiko Nakao, Hiroshi Haji, Shojiro Nakashima, Yasuhiro Sakamoto, Ryuichi Ogawa, Yoshihiro |
author_facet | Yamashita, Saori Matsuda, Yayoi Muta, Hiroki Nagao, Toshihiko Nakao, Hiroshi Haji, Shojiro Nakashima, Yasuhiro Sakamoto, Ryuichi Ogawa, Yoshihiro |
author_sort | Yamashita, Saori |
collection | PubMed |
description | Background: Sarcoidosis is occasionally accompanied by hematologic malignancies, including lymphoma, called sarcoidosis-lymphoma syndrome. Although the mechanism underlying the induction of lymphomas is still unknown, understanding the immunological background of sarcoidosis could help explain the possible mechanisms of the induction of lymphomas. Case Presentation: A 52-year-old woman was diagnosed chronic thyroiditis with normal thyroid function. One year later, she underwent a screening chest radiograph and identified bilateral hilar adenopathy and mediastinum lymphadenopathy. Subsequent mediastinoscopy demonstrated sarcoidosis. Because of the lack of clinical symptoms, steroid treatment was not initiated and regular follow-up was performed. One and a half years after the diagnosis of chronic thyroiditis, she presented with rapid swelling of the thyroid gland. FDG-PET/CT showed intense uptake of FDG in the thyroid gland and multiple lymphadenopathy. Fine-needle aspiration (FNA) cytology of the thyroid gland was only suggestive of a lymphoproliferative disorder and did not provide a definitive diagnosis. Partial thyroidectomy was performed, and the pathology indicated diffuse large B-cell lymphoma (DLBCL) such as high-grade transformation of extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT) lymphoma. The results of an examination of a paraffin block histopathology specimen by fluorescence in-situ hybridization (FISH) detected BCL6 rearrangement (3q27), which is the most common chromosomal abnormality in DLBCL. After the treatment with R-EPOCH (rituximab, etoposide, vincristine, doxorubicin, cyclophosphamide, and prednisone) chemotherapy, the thyroid gland enlargement has improved markedly, while the lymph nodes remained swelling, that suggested lymph node involvements were due to sarcoidosis. Conclusions: Rapid swelling of the thyroid gland in the setting of chronic thyroiditis should raise suspicion for thyroid lymphoma. Furthermore, our present case might suggest that sarcoidosis accelerate the development and high-grade transformation of thyroid lymphoma. To our knowledge, this is the first reported case of sarcoidosis and primary thyroid lymphoma in the same patient. |
format | Online Article Text |
id | pubmed-8089818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-80898182021-05-06 Sarcoidosis-Lymphoma Syndrome Associated With Primary Thyroid Lymphoma: A Case Report Yamashita, Saori Matsuda, Yayoi Muta, Hiroki Nagao, Toshihiko Nakao, Hiroshi Haji, Shojiro Nakashima, Yasuhiro Sakamoto, Ryuichi Ogawa, Yoshihiro J Endocr Soc Thyroid Background: Sarcoidosis is occasionally accompanied by hematologic malignancies, including lymphoma, called sarcoidosis-lymphoma syndrome. Although the mechanism underlying the induction of lymphomas is still unknown, understanding the immunological background of sarcoidosis could help explain the possible mechanisms of the induction of lymphomas. Case Presentation: A 52-year-old woman was diagnosed chronic thyroiditis with normal thyroid function. One year later, she underwent a screening chest radiograph and identified bilateral hilar adenopathy and mediastinum lymphadenopathy. Subsequent mediastinoscopy demonstrated sarcoidosis. Because of the lack of clinical symptoms, steroid treatment was not initiated and regular follow-up was performed. One and a half years after the diagnosis of chronic thyroiditis, she presented with rapid swelling of the thyroid gland. FDG-PET/CT showed intense uptake of FDG in the thyroid gland and multiple lymphadenopathy. Fine-needle aspiration (FNA) cytology of the thyroid gland was only suggestive of a lymphoproliferative disorder and did not provide a definitive diagnosis. Partial thyroidectomy was performed, and the pathology indicated diffuse large B-cell lymphoma (DLBCL) such as high-grade transformation of extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT) lymphoma. The results of an examination of a paraffin block histopathology specimen by fluorescence in-situ hybridization (FISH) detected BCL6 rearrangement (3q27), which is the most common chromosomal abnormality in DLBCL. After the treatment with R-EPOCH (rituximab, etoposide, vincristine, doxorubicin, cyclophosphamide, and prednisone) chemotherapy, the thyroid gland enlargement has improved markedly, while the lymph nodes remained swelling, that suggested lymph node involvements were due to sarcoidosis. Conclusions: Rapid swelling of the thyroid gland in the setting of chronic thyroiditis should raise suspicion for thyroid lymphoma. Furthermore, our present case might suggest that sarcoidosis accelerate the development and high-grade transformation of thyroid lymphoma. To our knowledge, this is the first reported case of sarcoidosis and primary thyroid lymphoma in the same patient. Oxford University Press 2021-05-03 /pmc/articles/PMC8089818/ http://dx.doi.org/10.1210/jendso/bvab048.1837 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Thyroid Yamashita, Saori Matsuda, Yayoi Muta, Hiroki Nagao, Toshihiko Nakao, Hiroshi Haji, Shojiro Nakashima, Yasuhiro Sakamoto, Ryuichi Ogawa, Yoshihiro Sarcoidosis-Lymphoma Syndrome Associated With Primary Thyroid Lymphoma: A Case Report |
title | Sarcoidosis-Lymphoma Syndrome Associated With Primary Thyroid Lymphoma: A Case Report |
title_full | Sarcoidosis-Lymphoma Syndrome Associated With Primary Thyroid Lymphoma: A Case Report |
title_fullStr | Sarcoidosis-Lymphoma Syndrome Associated With Primary Thyroid Lymphoma: A Case Report |
title_full_unstemmed | Sarcoidosis-Lymphoma Syndrome Associated With Primary Thyroid Lymphoma: A Case Report |
title_short | Sarcoidosis-Lymphoma Syndrome Associated With Primary Thyroid Lymphoma: A Case Report |
title_sort | sarcoidosis-lymphoma syndrome associated with primary thyroid lymphoma: a case report |
topic | Thyroid |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089818/ http://dx.doi.org/10.1210/jendso/bvab048.1837 |
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