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A rare case of isolated splenic sarcoidosis: A case report and literature review
Sarcoidosis is a multisystemic granulomatous disease. It is rarely isolated in the spleen. The present report describes a case of isolated splenic sarcoidosis that was diagnosed histologically following laparoscopic splenectomy. A 76-year-old woman, who underwent radical nephroureterectomy 7 years e...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739843/ https://www.ncbi.nlm.nih.gov/pubmed/33335730 http://dx.doi.org/10.3892/mco.2020.2184 |
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author | Kobayashi, Kazuki Einama, Takahiro Fujinuma, Ibuki Tsunenari, Takazumi Miyata, Yoichi Iwasaki, Toshimitsu Asakuma, Junichi Soga, Shigeyoshi Shinmoto, Hiroshi Tsujimoto, Hironori Hase, Kazuo Ueno, Hideki Kishi, Yoji |
author_facet | Kobayashi, Kazuki Einama, Takahiro Fujinuma, Ibuki Tsunenari, Takazumi Miyata, Yoichi Iwasaki, Toshimitsu Asakuma, Junichi Soga, Shigeyoshi Shinmoto, Hiroshi Tsujimoto, Hironori Hase, Kazuo Ueno, Hideki Kishi, Yoji |
author_sort | Kobayashi, Kazuki |
collection | PubMed |
description | Sarcoidosis is a multisystemic granulomatous disease. It is rarely isolated in the spleen. The present report describes a case of isolated splenic sarcoidosis that was diagnosed histologically following laparoscopic splenectomy. A 76-year-old woman, who underwent radical nephroureterectomy 7 years earlier for left renal pelvic cancer and mastectomy 6 years earlier for left breast cancer in another facility, was referred to our hospital for assessment of splenic tumors that were identified during a follow-up examination. The computed tomography scans revealed multiple nodules in the spleen, which had increased in size over 2 years. Positron emission tomography revealed accumulation of [18F]-fluorodeoxyglucose in the spleen. Laparoscopic splenectomy was performed and the diagnosis of sarcoidosis was confirmed histologically. A review of previous reports and the present case suggested that diagnosis of splenic sarcoidosis should be considered when the CT scans show multinodular splenic tumors, and sarcoidosis might be associated with malignant tumors. |
format | Online Article Text |
id | pubmed-7739843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-77398432020-12-16 A rare case of isolated splenic sarcoidosis: A case report and literature review Kobayashi, Kazuki Einama, Takahiro Fujinuma, Ibuki Tsunenari, Takazumi Miyata, Yoichi Iwasaki, Toshimitsu Asakuma, Junichi Soga, Shigeyoshi Shinmoto, Hiroshi Tsujimoto, Hironori Hase, Kazuo Ueno, Hideki Kishi, Yoji Mol Clin Oncol Articles Sarcoidosis is a multisystemic granulomatous disease. It is rarely isolated in the spleen. The present report describes a case of isolated splenic sarcoidosis that was diagnosed histologically following laparoscopic splenectomy. A 76-year-old woman, who underwent radical nephroureterectomy 7 years earlier for left renal pelvic cancer and mastectomy 6 years earlier for left breast cancer in another facility, was referred to our hospital for assessment of splenic tumors that were identified during a follow-up examination. The computed tomography scans revealed multiple nodules in the spleen, which had increased in size over 2 years. Positron emission tomography revealed accumulation of [18F]-fluorodeoxyglucose in the spleen. Laparoscopic splenectomy was performed and the diagnosis of sarcoidosis was confirmed histologically. A review of previous reports and the present case suggested that diagnosis of splenic sarcoidosis should be considered when the CT scans show multinodular splenic tumors, and sarcoidosis might be associated with malignant tumors. D.A. Spandidos 2021-02 2020-12-03 /pmc/articles/PMC7739843/ /pubmed/33335730 http://dx.doi.org/10.3892/mco.2020.2184 Text en Copyright: © Kobayashi et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Kobayashi, Kazuki Einama, Takahiro Fujinuma, Ibuki Tsunenari, Takazumi Miyata, Yoichi Iwasaki, Toshimitsu Asakuma, Junichi Soga, Shigeyoshi Shinmoto, Hiroshi Tsujimoto, Hironori Hase, Kazuo Ueno, Hideki Kishi, Yoji A rare case of isolated splenic sarcoidosis: A case report and literature review |
title | A rare case of isolated splenic sarcoidosis: A case report and literature review |
title_full | A rare case of isolated splenic sarcoidosis: A case report and literature review |
title_fullStr | A rare case of isolated splenic sarcoidosis: A case report and literature review |
title_full_unstemmed | A rare case of isolated splenic sarcoidosis: A case report and literature review |
title_short | A rare case of isolated splenic sarcoidosis: A case report and literature review |
title_sort | rare case of isolated splenic sarcoidosis: a case report and literature review |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739843/ https://www.ncbi.nlm.nih.gov/pubmed/33335730 http://dx.doi.org/10.3892/mco.2020.2184 |
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