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Right femoral pathological fracture caused by primary bone epithelioid angiosarcoma: Case report
RATIONALE: Epithelioid angiosarcoma (EAS) is an extremely rare malignant disease, which accounts no more than 1% of all soft tissue sarcomas. In this article, we would report a new case of EAS with multiple bone destruction and right femoral pathological fracture, which was an even rarer manifestati...
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/PMC5502134/ https://www.ncbi.nlm.nih.gov/pubmed/28682861 http://dx.doi.org/10.1097/MD.0000000000006951 |
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author | Li, Yatong Zou, Xiongfei Chang, Xiaoyan Chang, Xiao Sun, Shengfang Zhang, Baozhong |
author_facet | Li, Yatong Zou, Xiongfei Chang, Xiaoyan Chang, Xiao Sun, Shengfang Zhang, Baozhong |
author_sort | Li, Yatong |
collection | PubMed |
description | RATIONALE: Epithelioid angiosarcoma (EAS) is an extremely rare malignant disease, which accounts no more than 1% of all soft tissue sarcomas. In this article, we would report a new case of EAS with multiple bone destruction and right femoral pathological fracture, which was an even rarer manifestation of EAS. PATIENT CONCERNS: In this case, a 64-year-old man with right femoral fracture was reported. He had suffered from a progressive low back pain for about 8 months, and the imaging examinations prompted a multiple bone destruction in his vertebra and lower limbs. He then got a right femoral fracture without any obvious traumatic injury, and came to our hospital. INTERVENTIONS: He underwent an operation of radical resection, bone cement filling and dynamic condylar screw internal fixation. During the operation, we found that the soft tissue around the fracture had a rotten fish change, which suggested a malignant disease. DIAGNOSES: The postoperative pathological diagnosis reported an EAS, which is extremely rare and highly malignant. OUTCOMES: The patient died in 83 days after the surgery, and the survival time from the symptoms started to the end was only 11 months, which showed a rapid progress and poor prognosis of EAS. LESSONS: EAS is very hard to be diagnosed by clinical manifestation or radiological examinations. As in our case, pathological analysis is the final diagnosis. The images of the patient may offer some tips for the skeletal presentation of EAS, and do more help in future study of this disease. |
format | Online Article Text |
id | pubmed-5502134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-55021342017-07-18 Right femoral pathological fracture caused by primary bone epithelioid angiosarcoma: Case report Li, Yatong Zou, Xiongfei Chang, Xiaoyan Chang, Xiao Sun, Shengfang Zhang, Baozhong Medicine (Baltimore) 5700 RATIONALE: Epithelioid angiosarcoma (EAS) is an extremely rare malignant disease, which accounts no more than 1% of all soft tissue sarcomas. In this article, we would report a new case of EAS with multiple bone destruction and right femoral pathological fracture, which was an even rarer manifestation of EAS. PATIENT CONCERNS: In this case, a 64-year-old man with right femoral fracture was reported. He had suffered from a progressive low back pain for about 8 months, and the imaging examinations prompted a multiple bone destruction in his vertebra and lower limbs. He then got a right femoral fracture without any obvious traumatic injury, and came to our hospital. INTERVENTIONS: He underwent an operation of radical resection, bone cement filling and dynamic condylar screw internal fixation. During the operation, we found that the soft tissue around the fracture had a rotten fish change, which suggested a malignant disease. DIAGNOSES: The postoperative pathological diagnosis reported an EAS, which is extremely rare and highly malignant. OUTCOMES: The patient died in 83 days after the surgery, and the survival time from the symptoms started to the end was only 11 months, which showed a rapid progress and poor prognosis of EAS. LESSONS: EAS is very hard to be diagnosed by clinical manifestation or radiological examinations. As in our case, pathological analysis is the final diagnosis. The images of the patient may offer some tips for the skeletal presentation of EAS, and do more help in future study of this disease. Wolters Kluwer Health 2017-07-07 /pmc/articles/PMC5502134/ /pubmed/28682861 http://dx.doi.org/10.1097/MD.0000000000006951 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-sa/4.0 This is an open access article distributed under the Creative Commons Attribution-ShareAlike License 4.0, which allows others to remix, tweak, and build upon the work, even for commercial purposes, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-sa/4.0 |
spellingShingle | 5700 Li, Yatong Zou, Xiongfei Chang, Xiaoyan Chang, Xiao Sun, Shengfang Zhang, Baozhong Right femoral pathological fracture caused by primary bone epithelioid angiosarcoma: Case report |
title | Right femoral pathological fracture caused by primary bone epithelioid angiosarcoma: Case report |
title_full | Right femoral pathological fracture caused by primary bone epithelioid angiosarcoma: Case report |
title_fullStr | Right femoral pathological fracture caused by primary bone epithelioid angiosarcoma: Case report |
title_full_unstemmed | Right femoral pathological fracture caused by primary bone epithelioid angiosarcoma: Case report |
title_short | Right femoral pathological fracture caused by primary bone epithelioid angiosarcoma: Case report |
title_sort | right femoral pathological fracture caused by primary bone epithelioid angiosarcoma: case report |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502134/ https://www.ncbi.nlm.nih.gov/pubmed/28682861 http://dx.doi.org/10.1097/MD.0000000000006951 |
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