A 65-year-old man was referred for a nodular and ulcerated tumour on the right foot which started four months earlier. The diagnosis of cutaneous angiosarcoma was made based on histology and immunohistochemistry. Growth of Cutaneous angiosarcoma may be encouraged by the presence of a congenital or acquired chronic lymphoedema, irradiation sites and chronic ulceration. Cutaneous angiosarcoma is a rare kind of tumour with an aggressive course and a poor prognosis. Methods of treatment are surgical, radiotherapy, and chemotherapy. Fitzpatrick skin type (FST) phototype 6.
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