Intimal angiosarcomas are rare and difficult to diagnose preoperatively. Complete surgical resection is essential, but long-term survival is unlikely. We report a patient who presented with a contained ruptured infrarenal aorta with clinical and radiologic findings suggestive of infectious aortitis. Surgical resection, regional debridement, and reconstruction were completed using a cadaveric arterial homograft. However, pathologic evaluation revealed a high-grade intimal sarcoma
Aortic angiosarcoma is a rare, malignant neoplasm of the vasculature, with 24 case reports in the li...
The overall incidence of cardiac tumor is very low, and malignant cardiac tumors account for only 25...
Epithelioid angiosarcomas of the aorta are extremely rare neoplasms with only 26 previous reports in...
Although extremely rare, the group of primary malignant tumors of the aorta (PMTA) exhibits enormous...
Intimal angiosarcoma is a most unexpected cause of aortic occlusion. We present the case of a 74-yea...
Aortic angiosarcoma is an exceedingly rare clinical entity. Significant delay in diagnosis can occur...
AbstractPrimary malignant tumours of the abdominal aorta are rare and they are usually associated wi...
Introduction Epithelioid angiosarcoma is a rare soft tissue sarcoma with a poor prognosis. We report...
A 76-year-old male presented with recurrent claudication. A duplex scan showed an occluded superfici...
AbstractPrimary malignant tumors of the thoracic and abdominal aortas are extremely rare. In most ca...
Intimal angiosarcoma is a rare malignant vascular tumor with an aggressive natural history. Presenti...
Aortic dissection is a sudden and often dramatic event in which the blood passes through a tear in t...
SummaryThe overall incidence of cardiac tumor is very low, and malignant cardiac tumors account for ...
We report a rare case of angiosarcoma involving the gastrointestinal tract, liver, spleen, pancreas,...
Primary tumors of the aorta are extremely rare and the diagnosis is made most often after surgery or...
Aortic angiosarcoma is a rare, malignant neoplasm of the vasculature, with 24 case reports in the li...
The overall incidence of cardiac tumor is very low, and malignant cardiac tumors account for only 25...
Epithelioid angiosarcomas of the aorta are extremely rare neoplasms with only 26 previous reports in...
Although extremely rare, the group of primary malignant tumors of the aorta (PMTA) exhibits enormous...
Intimal angiosarcoma is a most unexpected cause of aortic occlusion. We present the case of a 74-yea...
Aortic angiosarcoma is an exceedingly rare clinical entity. Significant delay in diagnosis can occur...
AbstractPrimary malignant tumours of the abdominal aorta are rare and they are usually associated wi...
Introduction Epithelioid angiosarcoma is a rare soft tissue sarcoma with a poor prognosis. We report...
A 76-year-old male presented with recurrent claudication. A duplex scan showed an occluded superfici...
AbstractPrimary malignant tumors of the thoracic and abdominal aortas are extremely rare. In most ca...
Intimal angiosarcoma is a rare malignant vascular tumor with an aggressive natural history. Presenti...
Aortic dissection is a sudden and often dramatic event in which the blood passes through a tear in t...
SummaryThe overall incidence of cardiac tumor is very low, and malignant cardiac tumors account for ...
We report a rare case of angiosarcoma involving the gastrointestinal tract, liver, spleen, pancreas,...
Primary tumors of the aorta are extremely rare and the diagnosis is made most often after surgery or...
Aortic angiosarcoma is a rare, malignant neoplasm of the vasculature, with 24 case reports in the li...
The overall incidence of cardiac tumor is very low, and malignant cardiac tumors account for only 25...
Epithelioid angiosarcomas of the aorta are extremely rare neoplasms with only 26 previous reports in...