Dermatofibrosarcoma Explosive

Dermatofibrosarcoma is an uncommon epithelial tumor. The term "dermatofibosarcoma" was introduced into scientific use in 1864 by the French surgeon Wirth to designate this malignant tumor. There are a fair number of synonyms and descriptions of the disease. Currently, terms such as fibrous histiocytoma or Wade's tumor are found in the scientific literature.

Etiology Histological studies have shown that the neoplasm differs from benign nevi in ​​the presence of tumor cells with nuclei and intracellular granules involved in malignant growth. Develops quickly. It is a primary infiltrative tumor of the flat dermal layer (the process develops through a cell or through aggressive epithelial invasion). She looks like a devil

Dermatofibrosarcoma is a rare type of cancer of soft tissue and subcutaneous fat. Although it was first described in 1824, the scientific name comes from terms proposed by English pathologists in the 40s and 50s of the 20th century, A. Joubert and R. Douglas. The name comes from the word "fibro", which means "fiber" due to the fact that the tumor consists mainly of long and thin collagen fibers that form characteristic papillae and cysts. Another remarkable property of the neoplasm is its ability to spontaneously ulcerate with subsequent formation of wounds. **Why such a name as dermatofibrosis fibroroma falls?** In 1764, the English military surgeon D. Undernight conducted a macroscopic analysis of a number of skin tumors, noting among them a uniform (without