Testicular mesothelioma

Testicular mesothelioma is a rare cancer characterized by the development of a tumor from the mesothelial cells that line the surface of the testicles. This disease occurs in men aged 30 to 60 years and most often manifests itself in the form of a tumor, which can be either benign or malignant.

Symptoms of testicular mesothelioma may include testicular pain, enlarged testicles, urinary and erectile dysfunction, and blood in the urine. If the tumor is malignant, it can spread to other organs and tissues, which can lead to serious complications.

To diagnose testicular mesothelioma, ultrasound, MRI or CT is performed. Treatment may include surgical removal of the tumor, chemotherapy, or radiation therapy. The prognosis for testicular mesothelioma depends on the stage of the disease and the presence of complications.

Testicular mesothelial tumor is a rare cancer that can occur in men of any age. It is a cancer of the intrareticular tumor cell of the membrane layer lining the abdominal cavity and organs of the genitourinary system. Mesothelial testicular cancer can manifest itself as tumors in the groin, lower abdomen or scrotum, localized primarily in the right testicle, but can also be located in the left organ.

Causes of mesothelial tumor One of the causes of the disease is considered to be the papilloma virus