A RARE CLINICAL CASE: EWING'S SARCOMA OF THE SCROTUM

EWING'S SARCOMA IS A HIGHLY AGGRESSIVE MALIGNANT NEOPLASM THAT PRIMARILY AFFECTS THE SKELETAL SYSTEM AND PARAOSSEOUS SOFT TISSUES. EXTRAOSSEOUS FORMS OF EWING'S SARCOMA ACCOUNT FOR LESS THAN 1% OF ALL SARCOMA CASES, WITH THE GENITOURINARY SYSTEM BEING THEIR RAREST LOCALIZATION. CURRENTLY, THERE ARE NO SEPARATE GENERALLY ACCEPTED CLINICAL GUIDELINES FOR THE TREATMENT OF PATIENTS WITH EWING'S SARCOMA FAMILY TUMORS IN UROLOGY, AND THE TREATMENT OF EXTRAOSSEOUS FORMS IS CARRIED OUT ACCORDING TO THE PRINCIPLES OF TREATING SOFT TISSUE SARCOMAS. A CLINICAL CASE OF DIAGNOSIS AND TREATMENT OF EWING'S SARCOMA OF THE SCROTUM IN A 28-YEAR-OLD MAN IN THE ONCOLOGY-UROLOGY DEPARTMENT OF THE NOVOSIBIRSK REGION CITY CLINICAL HOSPITAL NO. 1, HOSPITALIZED WITH SUSPECTED NEOPLASM OF THE RIGHT TESTICLE, IS PRESENTED.