Ewing Tumor

Ewing's tumor, or jungisarcoma, is a malignant tumor that originates from connective tissue and develops in the bone. It is extremely rare in adults. At the same time, almost a third of all childhood tumors are cancerous. Tumors form both in and outside the bones. But the majority develops in the musculoskeletal system. Jungasarcoma can also form in soft tissues and nerve sheaths.

The disease has some symmetry: most often defects are detected in the right half of the body or the right side of the skull. Mainly affected elements of the axial skeleton (next



Ewing is a malignant tumor arising from primitive nerve cells. The pathogenesis of these neoplasms remains unclear. The largest number of these tumors occur in children. Detection is important due to tumor metastasis, which most often affects the central nervous system and bones. This tumor is characterized by rapid growth, an abundance of relapses, and early diagnosis has not yet been developed. Treatment depends on the histological type of tumor. Neoplasms such as Neurofibromas must be excised with or without adjacent fatty tissue. However, this procedure does not guarantee against possible relapse. Mostly such children are shown



Ewing's tumor is a rare disease associated with the proliferation of osteosarcoma and polymorphic connective tissue in bones and soft tissues. This type of tumor is a malignant neoplasm that develops from the endothelium, the inner lining of blood vessels. The pathology was named after the American



Article: Ewing's tumor (J. Ewing, 1876-1259, American pathologist; synonym: Omoblastoma of bone, Endothelioma of Bone Diffuse, Ewing's disease of bone, Diffuse Endotheliomas of Bone Ewing's sarcoma of bone)

Ewing tumor, also known as disseminated endodermal bone lesion and more commonly known as J. Ewing disease, is a rare type of soft tissue sarcoma of endothelial cells. This type of tumor occurs during childhood or adolescence and can affect various areas of the body, especially the bones. Tumors can develop anywhere in the bone without the ability to determine its original location. They rarely affect the nervous system.