Objective. We describe specific surgical methods for angiosarcoma regarding extent of resection and reconstructive options and assess their effect on patients’ prognosis. Patients and Methods. We retrospectively examined 14 patients undergoing treatment for angiosarcoma of the scalp at our institute between January 2000 and June 2015. Surgical treatment comprised wide excision of the tumor and reconstruction using a free flap with skin graft. Kaplan-Meier survival analysis was used to assess the survival parameters. Univariate and multivariate analyses were performed to evaluate the association between risk factors and outcome parameters. Results. Mean patient age at diagnosis was 69 years, and the mean follow-up period was 17 months. The o...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
none14siBACKGROUND: Angiosarcoma of bone is a rare high-grade malignant vascular tumor. The literat...
Angiosarcoma is a soft tissue tumour with a dismal prognosis. We present a 74 year old male presenti...
BACKGROUND Angiosarcoma is a malignant tumor of vascular endothelial cells that arises in the head ...
AbstractBackgroundScalp angiosarcoma is a rare soft tissue sarcoma with a very poor prognosis and hi...
[[abstract]]Background: Scalp angiosarcomas (AS) are aggressive soft tissue sarcomas that present wi...
Angiosarcoma is a relatively rare soft tissue tumour. It usually occurs in the head and neck, and es...
PURPOSE: Angiosarcoma is a rare vascular malignancy, and there are few published data to guide chemo...
Scalp angiosarcoma is a rare and highly malignant tumour originating from endothelial cells of vesse...
Purpose: Angiosarcoma of the scalp is unusual vascular tumor originating from endothelial cell. Angi...
Angiosarcomas are rare neoplasms of the head and neck region accounting for less than 1 % of maligna...
Introduction Angiosarcoma of the head and neck is a rare vascular sarcoma associated with high rates...
Cutaneous angiosarcoma is a rare and aggressive malignant tumor of vascular origin. Multimodality tr...
Angiosarcoma is a rare soft tissue sarcoma of poor prognosis. A retrospective single-center study wa...
BACKGROUND: The etiology of cutaneous angiosarcoma (cAS) may be idiopathic (I-cAS), or arise seconda...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
none14siBACKGROUND: Angiosarcoma of bone is a rare high-grade malignant vascular tumor. The literat...
Angiosarcoma is a soft tissue tumour with a dismal prognosis. We present a 74 year old male presenti...
BACKGROUND Angiosarcoma is a malignant tumor of vascular endothelial cells that arises in the head ...
AbstractBackgroundScalp angiosarcoma is a rare soft tissue sarcoma with a very poor prognosis and hi...
[[abstract]]Background: Scalp angiosarcomas (AS) are aggressive soft tissue sarcomas that present wi...
Angiosarcoma is a relatively rare soft tissue tumour. It usually occurs in the head and neck, and es...
PURPOSE: Angiosarcoma is a rare vascular malignancy, and there are few published data to guide chemo...
Scalp angiosarcoma is a rare and highly malignant tumour originating from endothelial cells of vesse...
Purpose: Angiosarcoma of the scalp is unusual vascular tumor originating from endothelial cell. Angi...
Angiosarcomas are rare neoplasms of the head and neck region accounting for less than 1 % of maligna...
Introduction Angiosarcoma of the head and neck is a rare vascular sarcoma associated with high rates...
Cutaneous angiosarcoma is a rare and aggressive malignant tumor of vascular origin. Multimodality tr...
Angiosarcoma is a rare soft tissue sarcoma of poor prognosis. A retrospective single-center study wa...
BACKGROUND: The etiology of cutaneous angiosarcoma (cAS) may be idiopathic (I-cAS), or arise seconda...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
none14siBACKGROUND: Angiosarcoma of bone is a rare high-grade malignant vascular tumor. The literat...
Angiosarcoma is a soft tissue tumour with a dismal prognosis. We present a 74 year old male presenti...