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  2. Content medically reviewed by
    Dr. Shreenidhi Kulkarniverified specialist
    MS, Orthopaedics
    View full profile onLinkedIn logoLinkedIn
    Your provider may recommend one or more of these tests.
    Chondrosarcoma is a slow growing tumor that is often diagnosed incidentally. Imaging tests and biopsy are performed.
    Common tests & procedures

    Imaging tests: Such as X ray, CT scan, MRI and bone scan help determine the tumor's location, size, and shape, and also assess the damage and extent of spread.

    Biopsy: A tissue sample from the affected region is taken for further examination and staging.

    Source: Focus Medica . For informational purposes only. Consult a medical professional for advice. Learn more
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    What is mesenchymal chondrosarcoma?NORD gratefully acknowledges Robert G. Maki, MD, PhD, Department of Medicine, Mount Sinai School of Medicine, New York, NY, for assistance in the preparation of this report. Mesenchymal chondrosarcoma is an extremely rare, often aggressive form of cancer. It is an uncommon type of chondrosarcoma.
    Can a parathyroid adenoma develop into cancer?
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    Dr. Himanshu J. Vats

    Doctor of Medicine (MBBS) · 1.5 years of exp

    A parathyroid adenoma is a non-cancerous (benign) tumor that grows in one of the four parathyroid glands. The parathyroid glands are located in the neck, near the thyroid gland. They produce parathyroid hormone (PTH), which helps to regulate the body's calcium levels. Parathyroid adenomas are the most common type of parathyroid tumor. They are usually small and do not cause any symptoms. In some cases, however, parathyroid adenomas can grow large enough to cause hyperparathyroidism, a condition where the body has too much calcium. Hyperparathyroidism can cause symptoms such as fatigue, muscle weakness, kidney stones, and bone loss.
    Q&A: Hyperparathyroidism
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    Are metastases common in mesenchymal chondrosarcoma (MCs)?Metastases were common at initial presentation and more commonly seen with larger tumors. Mesenchymal chondrosarcoma (MCS) is a rare, high-grade malignancy first described in 1959 by the pathologists Lichtenstein and Bernstein [ 1] as an unusual variant of chondrosarcoma affecting bone and soft tissues.
    Does mesenchymal chondrosarcoma have a worse prognosis?In comparison to conventional chondrosarcoma, which has a 10-year overall survival rate of 60% to 70% [ 6, 7, 9 ], the mesenchymal subtype is believed to portend a worse prognosis [ 2, 14, 17 ].
     
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