Cargando…

Concealed primary aortic sarcoma induced hypertensive encephalopathy resulting from a thoracic aortic occlusion: a case report

Primary aortic sarcoma is a rare condition that is frequently associated with distal embolization. In addition, growth characteristics of primary aortic sarcoma lead to the narrowing of the involved aortic lumen. A 72-year-old Korean male with primary aortic sarcoma showed progressive unexplained bl...

Descripción completa

Detalles Bibliográficos
Autores principales: Choi, Hyunmin, Yoon, Hee-Jeoung, Jang, Woo-Ik, Kim, Chang-Young, Doh, Joon-Hyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658867/
https://www.ncbi.nlm.nih.gov/pubmed/23597173
http://dx.doi.org/10.1186/1749-8090-8-102
_version_ 1782270350139064320
author Choi, Hyunmin
Yoon, Hee-Jeoung
Jang, Woo-Ik
Kim, Chang-Young
Doh, Joon-Hyung
author_facet Choi, Hyunmin
Yoon, Hee-Jeoung
Jang, Woo-Ik
Kim, Chang-Young
Doh, Joon-Hyung
author_sort Choi, Hyunmin
collection PubMed
description Primary aortic sarcoma is a rare condition that is frequently associated with distal embolization. In addition, growth characteristics of primary aortic sarcoma lead to the narrowing of the involved aortic lumen. A 72-year-old Korean male with primary aortic sarcoma showed progressive unexplained blood pressure elevation that didn’t improve with additional antihypertensive drug therapy. Because follow-up measures were not taken, the patient ultimately developed hypertensive encephalopathy with concurrent embolic dissemination. Although we successfully performed open transcatheter embolectomy in both legs, the patient died because of multiple organ failure 3 days after surgery. Given the ominous prognosis for this condition, this case report highlights the fact that the value of early detection and prompt evaluation of altered vital signs should not be overemphasized. We describe a rare case of primary aortic sarcoma that showed hypertensive encephalopathy caused by thoracic aortic occlusion and also had embolic metastases to the lower extremities.
format Online
Article
Text
id pubmed-3658867
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-36588672013-05-21 Concealed primary aortic sarcoma induced hypertensive encephalopathy resulting from a thoracic aortic occlusion: a case report Choi, Hyunmin Yoon, Hee-Jeoung Jang, Woo-Ik Kim, Chang-Young Doh, Joon-Hyung J Cardiothorac Surg Case Report Primary aortic sarcoma is a rare condition that is frequently associated with distal embolization. In addition, growth characteristics of primary aortic sarcoma lead to the narrowing of the involved aortic lumen. A 72-year-old Korean male with primary aortic sarcoma showed progressive unexplained blood pressure elevation that didn’t improve with additional antihypertensive drug therapy. Because follow-up measures were not taken, the patient ultimately developed hypertensive encephalopathy with concurrent embolic dissemination. Although we successfully performed open transcatheter embolectomy in both legs, the patient died because of multiple organ failure 3 days after surgery. Given the ominous prognosis for this condition, this case report highlights the fact that the value of early detection and prompt evaluation of altered vital signs should not be overemphasized. We describe a rare case of primary aortic sarcoma that showed hypertensive encephalopathy caused by thoracic aortic occlusion and also had embolic metastases to the lower extremities. BioMed Central 2013-04-18 /pmc/articles/PMC3658867/ /pubmed/23597173 http://dx.doi.org/10.1186/1749-8090-8-102 Text en Copyright © 2013 Choi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Choi, Hyunmin
Yoon, Hee-Jeoung
Jang, Woo-Ik
Kim, Chang-Young
Doh, Joon-Hyung
Concealed primary aortic sarcoma induced hypertensive encephalopathy resulting from a thoracic aortic occlusion: a case report
title Concealed primary aortic sarcoma induced hypertensive encephalopathy resulting from a thoracic aortic occlusion: a case report
title_full Concealed primary aortic sarcoma induced hypertensive encephalopathy resulting from a thoracic aortic occlusion: a case report
title_fullStr Concealed primary aortic sarcoma induced hypertensive encephalopathy resulting from a thoracic aortic occlusion: a case report
title_full_unstemmed Concealed primary aortic sarcoma induced hypertensive encephalopathy resulting from a thoracic aortic occlusion: a case report
title_short Concealed primary aortic sarcoma induced hypertensive encephalopathy resulting from a thoracic aortic occlusion: a case report
title_sort concealed primary aortic sarcoma induced hypertensive encephalopathy resulting from a thoracic aortic occlusion: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658867/
https://www.ncbi.nlm.nih.gov/pubmed/23597173
http://dx.doi.org/10.1186/1749-8090-8-102
work_keys_str_mv AT choihyunmin concealedprimaryaorticsarcomainducedhypertensiveencephalopathyresultingfromathoracicaorticocclusionacasereport
AT yoonheejeoung concealedprimaryaorticsarcomainducedhypertensiveencephalopathyresultingfromathoracicaorticocclusionacasereport
AT jangwooik concealedprimaryaorticsarcomainducedhypertensiveencephalopathyresultingfromathoracicaorticocclusionacasereport
AT kimchangyoung concealedprimaryaorticsarcomainducedhypertensiveencephalopathyresultingfromathoracicaorticocclusionacasereport
AT dohjoonhyung concealedprimaryaorticsarcomainducedhypertensiveencephalopathyresultingfromathoracicaorticocclusionacasereport