Try adjusting your type
14th October, 2009
European Survey on Standards of Care in paediatric oncology centres. J. R. Kowalczyk, M. Samardakiewicz, K. Pritchard-Jones, R. Ladenstein, S. Essiaf, E. Fitzgerald, G. Petrarulo, G. Vassal - EJC , Volume 61, pp 11-19
8th December, 2014
The purpose of this website is to provide good and clear information about the long-term effects of childhood cancer and to refer to the various late-effects outpatient clinics (LATER outpatient clinics) that exist in the Netherlands.
8th September, 2015
Cancer in young people is rare, but it is still a major health issue in Europe. Each year, more than 6,000 young people in Europe die of cancer. There are more than 300,000 European childhood cancer survivors (in 2020, they will be nearly half a million): two-thirds of them have some late side effects of treatment, that are severe and impact on the daily life of half of those affected.
Angiosarcoma is a rare, malignant tumor that originates from endothelial cells, the cells that line the interior surface of blood vessels. It can occur anywhere in the body, but is most commonly found in the skin, breast, liver, spleen, and deep tissue. Due to its aggressive nature, it often leads to a poor prognosis. This tumor presents unique challenges due to its high recurrence rate and resistance to treatment.
There are several types of cancer that affect individuals worldwide, each possessing unique characteristics and challenges. One such condition is Angiosarcoma, a rare but aggressive form of cancer.
Cancer, in its most basic definition, is the overgrowth of cells in a specific part of the body. When the body’s natural ability to regulate cell growth is disrupted, it can result in the formation of a tumor, which can be harmless (benign) or potentially fatal (malignant). One such malignant tumor is Angiosarcoma.
Among the many types of cancer, angiosarcoma stands as one of the rarest. Angiosarcoma targets the endothelial cells lining the inner part of a person’s blood vessels, causing an abnormal and uncontrolled cell growth.
In medical terminology, angiosarcoma is a high-grade malignancy of endothelial cells. It’s invasive, spreads rapidly, and often exhibits extensively infiltrative borders. This cancer can develop anywhere in the body, but it most often found in the skin or the soft tissues beneath.
Angiosarcoma is classified into several types, depending on where it originates from within the body. Subcategories include cutaneous, breast, hepatic, and primary angiosarcoma of the spleen.
Scientific research has linked angiosarcoma to several genetic mutations. However, the exact cause is yet to be pinpointed. It’s clear, however, that environmental and lifestyle factors may increase the risk of developing this malignancy.
The precise mechanism by which angiosarcoma develops is still unknown. However, it’s generally understood that mutations cause endothelial cells to grow uncontrollably, thereby forming a tumor. Over time, some of these cells may break off and spread to other parts of the body, leading to metastasis.
Symptoms of angiosarcoma may vary greatly, depending on the area of the body affected. They may present as skin lesions that change in size, shape, and color. In more severe cases, there may be internal bleeding or pain.
Due to its aggressive nature, early diagnosis of angiosarcoma is paramount. Diagnostic procedures often include imaging tests, blood analysis, and possibly biopsy for histopathological examination.
The treatment of angiosarcoma often involves a combination of surgery, chemotherapy, and radiation therapy. The choice of treatment modality depends on the location, size, and extent of the cancer.
Angiosarcoma has an unpredictable prognosis, with survival rates varying significantly. Factors that determine prognosis include the size of the tumor, its location, and whether it has spread to other parts of the body.
Living with angiosarcoma presents its unique set of challenges. This journey resonates through the testimonies of individuals who’ve braved angiosarcoma, giving insights into their fights against this disease.
Supportive care is essential for angiosarcoma patients. Through psychotherapy and counseling, and the gathering of support from friends and family, patients can better cope with this challenging condition.
Angiosarcoma is a rare, high-grade malignancy with a varying and often unpredictable prognosis. Despite its aggressive nature, early detection, and comprehensive treatment strategies can provide hope for those diagnosed with this disease.
Medical research continues to make strides towards finding a cure for angiosarcoma. With advancements in genomics and other scientific domains, there is hope for more effective treatments and better prognoses in the future.
Angiosarcoma is a rare type of cancer that forms in the lining of blood vessels. It represents a small percentage of soft tissue sarcomas.
Yes, angiosarcoma is classified depending on where it originates from within the body. This includes cutaneous, breast, hepatic, and primary angiosarcoma of the spleen.
Diagnosis often involves imaging tests, blood analysis, and biopsy. Treatment strategies include surgery, chemotherapy, and radiation therapy.
Research has linked angiosarcoma to certain genetic mutations, but it’s not typically considered hereditary.
Survival rates vary significantly and depend on factors such as the size and location of the tumor and whether it has metastasized.
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