Poshi's sarcoma

Sarcomaka Poshi: description, treatment and prognosis

Sarcomaka Poshi (also known as superficial sarcomatosis) is a rare type of skin sarcoma that usually affects the extremities and trunk. Lymph nodes, internal organs and bones can also be affected, but this is much less common. This is a malignant disease that can be combined with immunodeficiency conditions and is characterized by a slow course.

Symptoms of Poshi's sarcomaca develop on the skin in the form of multiple exophytic formations that may be prone to ulceration. Gradually, these tumor nodules merge and form ulcerative surfaces of various sizes, which may be prone to infection. Underlying structures such as soft tissue and bone are also involved.

To treat Poshi's sarcomaca, surgery, radiation therapy and cytostatic ointments are used. In advanced cases of the disease, chemotherapy is used, which includes a combination of drugs such as dactinomycin, vincristine and adriamycin. Combinations including prospidin, cyclophosphamide and some other drugs are also effective.

The prognosis of Poshi's sarcoma depends on the stage of the disease and the effectiveness of treatment. Complete remission is achieved in 70% of cases, but relapses of the disease are not uncommon. Therefore, it is important to receive regular medical supervision after treatment.

Overall, Poshi's sarcoma is a rare but dangerous type of skin sarcoma. However, early consultation with a doctor, accurate diagnosis and timely treatment can improve the prognosis of the disease and help avoid serious complications.