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Malignant solitary fibrous tumor of the pancreas with systemic metastasis: A case report and review of the literature
BACKGROUND: Pancreatic solitary fibrous tumor (SFT) is a rare neoplasm of intermediate biological potential. So far, only 22 cases have been reported since 1999. All the cases, except one, exhibited benign features. Here, we report the first case of malignant pancreatic SFT with typical Doege-Potter...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000951/ https://www.ncbi.nlm.nih.gov/pubmed/32047784 http://dx.doi.org/10.12998/wjcc.v8.i2.343 |
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author | Geng, Hao Ye, Yu Jin, Yun Li, Bai-Zhou Yu, Yuan-Quan Feng, Yang-Yang Li, Jiang-Tao |
author_facet | Geng, Hao Ye, Yu Jin, Yun Li, Bai-Zhou Yu, Yuan-Quan Feng, Yang-Yang Li, Jiang-Tao |
author_sort | Geng, Hao |
collection | PubMed |
description | BACKGROUND: Pancreatic solitary fibrous tumor (SFT) is a rare neoplasm of intermediate biological potential. So far, only 22 cases have been reported since 1999. All the cases, except one, exhibited benign features. Here, we report the first case of malignant pancreatic SFT with typical Doege-Potter syndrome, along with the clinical and pathologic evidence of its systemic metastasis. CASE SUMMARY: The patient was a 48-year-old man with a 1-year history of pancreatic and liver masses and refractory hypoglycemia. Increased uptake of the tracer fluorodeoxyglucose (FDG) was found in the liver and bones by fluorine-18 FDG positron emission tomography/computed tomography. After multidisciplinary discussion, a distal pancreatectomy procedure was performed, and histological examination showed a lesion composed of abundant heterogeneous spindle cells with localized necrosis. On immunohistochemistry evaluation, STAT6 was found to be diffusely expressed in the tumor. Based on the overall evidence, the patient was diagnosed with malignant pancreatic SFT with liver and bone metastases. CONCLUSION: The diagnosis of malignant SFT requires comprehensive evidence including clinical, immunohistochemistry, and histological features. This case may be presented as a reference for diagnoses and management of malignant pancreatic SFTs with systemic metastasis. |
format | Online Article Text |
id | pubmed-7000951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-70009512020-02-11 Malignant solitary fibrous tumor of the pancreas with systemic metastasis: A case report and review of the literature Geng, Hao Ye, Yu Jin, Yun Li, Bai-Zhou Yu, Yuan-Quan Feng, Yang-Yang Li, Jiang-Tao World J Clin Cases Case Report BACKGROUND: Pancreatic solitary fibrous tumor (SFT) is a rare neoplasm of intermediate biological potential. So far, only 22 cases have been reported since 1999. All the cases, except one, exhibited benign features. Here, we report the first case of malignant pancreatic SFT with typical Doege-Potter syndrome, along with the clinical and pathologic evidence of its systemic metastasis. CASE SUMMARY: The patient was a 48-year-old man with a 1-year history of pancreatic and liver masses and refractory hypoglycemia. Increased uptake of the tracer fluorodeoxyglucose (FDG) was found in the liver and bones by fluorine-18 FDG positron emission tomography/computed tomography. After multidisciplinary discussion, a distal pancreatectomy procedure was performed, and histological examination showed a lesion composed of abundant heterogeneous spindle cells with localized necrosis. On immunohistochemistry evaluation, STAT6 was found to be diffusely expressed in the tumor. Based on the overall evidence, the patient was diagnosed with malignant pancreatic SFT with liver and bone metastases. CONCLUSION: The diagnosis of malignant SFT requires comprehensive evidence including clinical, immunohistochemistry, and histological features. This case may be presented as a reference for diagnoses and management of malignant pancreatic SFTs with systemic metastasis. Baishideng Publishing Group Inc 2020-01-26 2020-01-26 /pmc/articles/PMC7000951/ /pubmed/32047784 http://dx.doi.org/10.12998/wjcc.v8.i2.343 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Geng, Hao Ye, Yu Jin, Yun Li, Bai-Zhou Yu, Yuan-Quan Feng, Yang-Yang Li, Jiang-Tao Malignant solitary fibrous tumor of the pancreas with systemic metastasis: A case report and review of the literature |
title | Malignant solitary fibrous tumor of the pancreas with systemic metastasis: A case report and review of the literature |
title_full | Malignant solitary fibrous tumor of the pancreas with systemic metastasis: A case report and review of the literature |
title_fullStr | Malignant solitary fibrous tumor of the pancreas with systemic metastasis: A case report and review of the literature |
title_full_unstemmed | Malignant solitary fibrous tumor of the pancreas with systemic metastasis: A case report and review of the literature |
title_short | Malignant solitary fibrous tumor of the pancreas with systemic metastasis: A case report and review of the literature |
title_sort | malignant solitary fibrous tumor of the pancreas with systemic metastasis: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000951/ https://www.ncbi.nlm.nih.gov/pubmed/32047784 http://dx.doi.org/10.12998/wjcc.v8.i2.343 |
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