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Chondroblastoma is a rare, benign, locally aggressive bone tumor that typically affects the epiphyses or apophyses of long bones. [ 1 ] [ 2 ] It is thought to arise from an outgrowth of immature cartilage cells ( chondroblasts ) from secondary ossification centers , originating from the epiphyseal plate or some remnant of it.
General treatment regimens have not changed much in the past 30 years, in part due to the lack of randomized clinical trials. [4] Surgery is the treatment of choice if the tumor is determined to be resectable. Curettage is a commonly used technique. [12] The situation is complicated in a patient with a pathological fracture.
Osteochondroma is the most common benign tumor of bone. [1] [2] The tumors take the form of cartilage-capped bony projections or outgrowth on the surface of bones ().[3] [4] It is characterized as a type of overgrowth that can occur in any bone where cartilage forms bone.
Specific treatment for enchondroma is determined by a physician based on the age, overall health, and medical history of the patient. Other considerations include: extent of the disease; tolerance for specific medications, procedures, or therapies; expectations for the course of the disease; opinion or preference of the patient; Treatment may ...
Treatment - best left alone - if it causes fractures (enchondroma) or is unsightly it should be removed by curettage and the defect filled with bone graft. [1]
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