What is Angiosarcoma?
Angiosarcoma is a type of tumor that commonly develops in the lining of blood vessels.
The disease is aggressive, spreads fast, and has a high rate of recurrence locally.
Its origins can be in any part of the body but commonly arises in the skin, soft tissues, breasts, lungs, heart, liver, spleens, and bones.
The disease is aggressive, spreads fast, and has a high rate of recurrence locally.
Its origins can be in any part of the body but commonly arises in the skin, soft tissues, breasts, lungs, heart, liver, spleens, and bones.
Factors Contributing to Angiosarcoma
Factors that may have caused angiosarcoma include:*Radiotherapy
*Chronic lymphedema (or radical mastectomy)
*Foreign objects retained in the body (like plastic, steel, shrapnel, and Dacron vascular prosthesis)
*Environmental toxins:
Arsenic solutions that are sprayed on grapevines
Thorotrast (contrast agent that emits radiation)
Vinyl chloride (commercial chemical used in plastic and rubber industry)
Type of Tumor
Angiosarcoma is a type of tumor that commonly develops in the lining of blood vessels. Its origins can be in any part of the body but commonly arises in the skin, soft tissues, breasts, lungs, heart, liver, spleens, and bones.
Angiosarcoma Prognosis
Angiosarcoma prognosis is often poor because symptoms do not appear early or not specific.
However, the earlier angiosarcoma was diagnosed, the faster and more effective the treatment would be. The end result could be a better prognosis.
However, the earlier angiosarcoma was diagnosed, the faster and more effective the treatment would be. The end result could be a better prognosis.
“Prognosis of the disease becomes good when the tumor is limited to a primary site”
Factors Affecting Diagnosis
Here some factors that affect the diagnosis:
*Tumor size is often larger than what it shown externally.
*Treatments like chemotherapy sometimes cause development of angiosarcoma.
*Primary site of tumor may assist the disease to spread to other parts.
*The spread of tumor is wider and deeper than the result from tests.
Soft Tissue Angiosarcomas (extremities, abdominal wall, and retroperitoneum)
*MRI provides accurate delineation of local disease.
*CT scan (chest) is sensitive but not specific.
Bone Angiosarcoma
*Radiography result does not specify presentation but features high-grade lesions that destroy soft tissues.
*CT scan confirms insidious character of lesions and their multiplicity.
*MRI test findings help present involvement of neurovascular structures and extension of soft tissue.
*Bone scan helps form differential diagnosis with multifocal bone processes and multiple myeloma (or cell histiocytosis).
Cutaneous angiosarcoma
*CT scan helps identify disease on head and neck.
*MRI shows extent of bone and soft tissue involvement.
Prognosis of the disease becomes good when the tumor is limited to a primary site. It is known as malignant and aggressive but treatment options include:
*Surgical resection
*Radiotherapy
*Chemotherapy
*Medication with angiogenesis inhibitor
*Tumor size is often larger than what it shown externally.
*Treatments like chemotherapy sometimes cause development of angiosarcoma.
*Primary site of tumor may assist the disease to spread to other parts.
*The spread of tumor is wider and deeper than the result from tests.
Soft Tissue Angiosarcomas (extremities, abdominal wall, and retroperitoneum)
*MRI provides accurate delineation of local disease.
*CT scan (chest) is sensitive but not specific.
Bone Angiosarcoma
*Radiography result does not specify presentation but features high-grade lesions that destroy soft tissues.
*CT scan confirms insidious character of lesions and their multiplicity.
*MRI test findings help present involvement of neurovascular structures and extension of soft tissue.
*Bone scan helps form differential diagnosis with multifocal bone processes and multiple myeloma (or cell histiocytosis).
Cutaneous angiosarcoma
*CT scan helps identify disease on head and neck.
*MRI shows extent of bone and soft tissue involvement.
Prognosis of the disease becomes good when the tumor is limited to a primary site. It is known as malignant and aggressive but treatment options include:
*Surgical resection
*Radiotherapy
*Chemotherapy
*Medication with angiogenesis inhibitor
Angiosarcoma Law Blog
Angiosarcoma
- Cancer sufferer with no nose left struggling to breath at the PRU
- Mrs Searle, from Halstead in Kent, has had problems breathing since she had her nose removed in February 2011 as part of her treatment for a rare form of cancer known as angiosarcoma. The grandmother-of-seven, who was being treated for cellulitis in ...
- Cancer specialist's husband pays tribute to her 'strength'
- Dr Helen Patterson, lead clinician for prostate cancer at Addenbrooke's, died last month aged 49 after a long battle with angiosarcoma ? cancer of the blood vessel lining. She had studied sarcomas for her PhD, but the form she developed was very rare.
- Alford's fight inspires Chiles baseball team
- This latest diagnosis showed the cancer ? angiosarcoma ? had moved to a spot that made chemotherapy difficult. ?It was pretty much in the lung and a little bit up around the heart,? said Bill Alford, Chris' father. ?That was the doctors' concern.
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