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Primary atrial fibromyxosarcoma with multiple-system metastases: A case report
RATIONALE: Fibromyxosarcoma is common in head and neck, vessel, omentum, and reproductive system, with low-grade malignant behavior. However, primary atrial fibromyxosarcoma with highly malignant behavior is extremely rare. PATIENT CONCERNS: A 34-year-old female presented with oppression in the ches...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728873/ https://www.ncbi.nlm.nih.gov/pubmed/29245258 http://dx.doi.org/10.1097/MD.0000000000008930 |
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author | Qiu, Jingping Tang, Lingrong Han, Yang Wang, Chun Gu, Tianxiang Li, Guang |
author_facet | Qiu, Jingping Tang, Lingrong Han, Yang Wang, Chun Gu, Tianxiang Li, Guang |
author_sort | Qiu, Jingping |
collection | PubMed |
description | RATIONALE: Fibromyxosarcoma is common in head and neck, vessel, omentum, and reproductive system, with low-grade malignant behavior. However, primary atrial fibromyxosarcoma with highly malignant behavior is extremely rare. PATIENT CONCERNS: A 34-year-old female presented with oppression in the chest, short breath, and onset of headache as initial symptoms. The preoperative echocardiogram showed a medium-size echogenic mass close to the posterior leaflet of the mitral valve in the left atrium. DIAGNOSIS: Primary atrial fibromyxosarcoma with multiple-system metastases. INTERVENTIONS: The patient underwent surgery, and the tumor was removed completely. The diagnosis of left atrium fibromyxosarcoma was confirmed through postoperative histopathological examination. Positron emission tomography/computed tomography scan was performed, which revealed multiple metastases to left adnexa, bilateral adrenal glands, left iliacus, right lateral ventricle, and skeletal system. OUTCOMES: The patient died of cerebral hernia caused by hemorrhage from the metastatic brain tumor, 30 days after the surgery, without receiving chemotherapy or radiotherapy. LESSONS: Cardiac fibromyxosarcoma is a rare primary malignant cardiac neoplasm, probably with systemic metastases. The possibility of malignancy should be considered as differential diagnosis for cardiac mass. |
format | Online Article Text |
id | pubmed-5728873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-57288732017-12-20 Primary atrial fibromyxosarcoma with multiple-system metastases: A case report Qiu, Jingping Tang, Lingrong Han, Yang Wang, Chun Gu, Tianxiang Li, Guang Medicine (Baltimore) 5700 RATIONALE: Fibromyxosarcoma is common in head and neck, vessel, omentum, and reproductive system, with low-grade malignant behavior. However, primary atrial fibromyxosarcoma with highly malignant behavior is extremely rare. PATIENT CONCERNS: A 34-year-old female presented with oppression in the chest, short breath, and onset of headache as initial symptoms. The preoperative echocardiogram showed a medium-size echogenic mass close to the posterior leaflet of the mitral valve in the left atrium. DIAGNOSIS: Primary atrial fibromyxosarcoma with multiple-system metastases. INTERVENTIONS: The patient underwent surgery, and the tumor was removed completely. The diagnosis of left atrium fibromyxosarcoma was confirmed through postoperative histopathological examination. Positron emission tomography/computed tomography scan was performed, which revealed multiple metastases to left adnexa, bilateral adrenal glands, left iliacus, right lateral ventricle, and skeletal system. OUTCOMES: The patient died of cerebral hernia caused by hemorrhage from the metastatic brain tumor, 30 days after the surgery, without receiving chemotherapy or radiotherapy. LESSONS: Cardiac fibromyxosarcoma is a rare primary malignant cardiac neoplasm, probably with systemic metastases. The possibility of malignancy should be considered as differential diagnosis for cardiac mass. Wolters Kluwer Health 2017-12-08 /pmc/articles/PMC5728873/ /pubmed/29245258 http://dx.doi.org/10.1097/MD.0000000000008930 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0 |
spellingShingle | 5700 Qiu, Jingping Tang, Lingrong Han, Yang Wang, Chun Gu, Tianxiang Li, Guang Primary atrial fibromyxosarcoma with multiple-system metastases: A case report |
title | Primary atrial fibromyxosarcoma with multiple-system metastases: A case report |
title_full | Primary atrial fibromyxosarcoma with multiple-system metastases: A case report |
title_fullStr | Primary atrial fibromyxosarcoma with multiple-system metastases: A case report |
title_full_unstemmed | Primary atrial fibromyxosarcoma with multiple-system metastases: A case report |
title_short | Primary atrial fibromyxosarcoma with multiple-system metastases: A case report |
title_sort | primary atrial fibromyxosarcoma with multiple-system metastases: a case report |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728873/ https://www.ncbi.nlm.nih.gov/pubmed/29245258 http://dx.doi.org/10.1097/MD.0000000000008930 |
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