2011
DOI: 10.1007/s00270-011-0219-6
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Epithelioid Angiosarcoma With Metastatic Disease After Endovascular Therapy of Abdominal Aortic Aneurysm

Abstract: Malignancies of the aortic wall represent a rare condition, and only a few reports have covered cases of sarcomas arising at the site of a prosthesis made of Dacron. A coincidence with endovascular repair has only been reported in one case to date. We report a patient with epithelioid angiosarcoma and metastatic disease, which was found in an aneurysmal sac after endovascular aortic repair for abdominal aortic aneurysm.

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Cited by 23 publications
(25 citation statements)
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“…With respect to aortic endografts, some investigators have suggested an association between endograft infection and subsequent malignancy, although this remains speculative. 13,[17][18][19][20] While causality cannot be proven, other authors, like in our case, testify that malignancy was not seen at the time of surgical graft implantation and was not seen on pre-operative imaging at the time of endograft implantation. Furthermore, as in this case, the malignancy arises in the aortic wall adjacent to the graft.…”
Section: J O U R N a L P R E -P R O O Fmentioning
confidence: 44%
“…With respect to aortic endografts, some investigators have suggested an association between endograft infection and subsequent malignancy, although this remains speculative. 13,[17][18][19][20] While causality cannot be proven, other authors, like in our case, testify that malignancy was not seen at the time of surgical graft implantation and was not seen on pre-operative imaging at the time of endograft implantation. Furthermore, as in this case, the malignancy arises in the aortic wall adjacent to the graft.…”
Section: J O U R N a L P R E -P R O O Fmentioning
confidence: 44%
“…Histologically, the aortic sarcomas represent a heterogeneous group with major reported subtypes including angiosarcoma, leiomyosarcoma, fibrosarcoma, fibromyxosarcoma, fibroxanthosarcoma, and malignant fibrous histiocytoma [4]. Primary aortic angiosarcoma (2 of the 3 cases reported here; previously &35 reported cases) and primary aortic sarcoma arising after EVAR (all 3-cases in this report; previously 2 reported cases) are unique subsets of this pathology [2,3]. To our knowledge, the presented cases series is the largest describing primary aortic sarcomas in the setting of successful endovascular repair.…”
Section: Discussionmentioning
confidence: 67%
“…Since their first description in surgical literature by Brodowski in 1873, only approximately, 140 cases have been reported [1]. A unique subset of this rare pathology is aortic sarcomas arising after endovascular aneurysm repair (EVAR), reports of which are scarce in the published literature [2,3]. As the presenting symptoms can be non-specific and may be mistakenly attributed to more common aortic disease processes, the diagnosis of an underlying aortic malignancy can be challenging and often delayed.…”
Section: Introductionmentioning
confidence: 98%
“…[4] F-18 FDG PET/CT experiences in imaging angiosarcoma at anterior mediastinum, vessel, epicardium and adrenal gland were reported. [14][15][16][17] These reports have described variable F-18 FDG avidity of epithelioid angiosarcoma, which were mild to intense in F-18 FDG uptake (SUVmax up to 9.7). To our knowledge, the F-18 FDG PET/CT findings of primary uterine angiosarcoma have not been previously reported.…”
Section: Discussionmentioning
confidence: 96%