Intimal angiosarcoma is a most unexpected cause of aortic occlusion. We present the case of a 74-year-old woman with intimal angiosarcoma that manifested with the triad of congestive heart failure, acute renal failure, and abdominal angina. A review of the literature and discussion of postoperative outcomes follows
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...
Introduction Epithelioid angiosarcoma is a rare soft tissue sarcoma with a poor prognosis. We report...
Although extremely rare, the group of primary malignant tumors of the aorta (PMTA) exhibits enormous...
AbstractPrimary malignant tumors of the thoracic and abdominal aortas are extremely rare. In most ca...
AbstractPrimary malignant tumours of the abdominal aorta are rare and they are usually associated wi...
Intimal angiosarcomas are rare and difficult to diagnose preoperatively. Complete surgical resection...
INTRODUCTION: Primary angiosarcoma of the aorta is a rare malignancy arising from the aorta’s endoth...
IntroductionPrimary angiosarcomas of the aorta are rare and because of their non-specific presentati...
Aortic angiosarcoma is an exceedingly rare clinical entity. Significant delay in diagnosis can occur...
Aortic sarcomas have not been linked to Lynch syndrome in humans, although other soft tissue maligna...
We describe a 74-year-old male patient with an intimal sarcoma of the descending aorta mimicking aor...
Primary tumors originating within the wall of the arteries are rare and they frequently manifest lat...
SummaryThe overall incidence of cardiac tumor is very low, and malignant cardiac tumors account for ...
: Introduction: Primary angiosarcomas of the aorta are rare and because of their non-specific prese...
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...
Introduction Epithelioid angiosarcoma is a rare soft tissue sarcoma with a poor prognosis. We report...
Although extremely rare, the group of primary malignant tumors of the aorta (PMTA) exhibits enormous...
AbstractPrimary malignant tumors of the thoracic and abdominal aortas are extremely rare. In most ca...
AbstractPrimary malignant tumours of the abdominal aorta are rare and they are usually associated wi...
Intimal angiosarcomas are rare and difficult to diagnose preoperatively. Complete surgical resection...
INTRODUCTION: Primary angiosarcoma of the aorta is a rare malignancy arising from the aorta’s endoth...
IntroductionPrimary angiosarcomas of the aorta are rare and because of their non-specific presentati...
Aortic angiosarcoma is an exceedingly rare clinical entity. Significant delay in diagnosis can occur...
Aortic sarcomas have not been linked to Lynch syndrome in humans, although other soft tissue maligna...
We describe a 74-year-old male patient with an intimal sarcoma of the descending aorta mimicking aor...
Primary tumors originating within the wall of the arteries are rare and they frequently manifest lat...
SummaryThe overall incidence of cardiac tumor is very low, and malignant cardiac tumors account for ...
: Introduction: Primary angiosarcomas of the aorta are rare and because of their non-specific prese...
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...
Introduction Epithelioid angiosarcoma is a rare soft tissue sarcoma with a poor prognosis. We report...