Sarcoma is cancer that begins in the body's soft tissues, such as fat, muscles, nerves, tendons, blood vessels, and lymph vessels, and can occur anywhere in the body and any organ. The most common areas affected are arms and legs. These cancers do not cause symptoms early on, as the tissues' elastic nature accommodates the growing tumor. Symptoms only occur when the lump presses on a nerve, bone, blood vessel, or muscle or if a lump is visible. Inherited medical conditions, such as familial adenomatous polyposis (FAP), neurofibromatosis, Li-Fraumeni syndrome, and retinoblastoma, make a person more prone to soft tissue sarcoma.
Examples of these benign tumors are ossifying fibromyxoid tumor, perivascular epithelioid cell tumor, angiomyolipoma, and sugar cell tumor, lymphangioleiomyomatosis, giant cell tumor of the tendon sheath and pigmented villonodular synovitis, myoepithelial tumors of soft tissue, and glomus tissue tumor. Benign tumors that are the least aggressive are lipoma, lipomatosis, lipoblastoma or lipoblastomatosis, angiolipoma, angiomyolipoma, angiomyolipoma, hibernoma, granular cell tumors, elastoma, hemangioma, leiomyoma, schwannoma, neurofibroma, myxoma, angiomyxoma, and angiofibroma.
All cancer patients at MSK are offered compassionate and personalized care from their experts. Specialists experienced in surgery, chemotherapy, radiation therapy, rehabilitation, and maintaining the quality of life will work closely to develop a customized treatment plan to ensure the best outcome possible. Patients also benefit from new chemotherapy drugs through thousands of ongoing clinical trials at MSK. MSK doctors see more than 600 new patients with sarcoma every year and operate on tumors considered inoperable by other cancer centers. They have published their experience in diagnosing and treating more than 10,000 patients with soft tissue sarcoma.
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