Heterotopic Ossification Research Paper

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The disease I am going to discuss in this paper is Heterotopic Ossification (HO). According to Goodman, Fuller, and O’Shea (2012), Heterotopic Ossification is defined as bone formation in nonosseous tissues (forms the rigid part of the bones that make up the skeletal system), and is considered a benign condition of abnormal bone formation in soft tissue. (pg. 666)
According to numerous references and medical websites, I have found no known cause of HO. It is presumed by Chao, Suh, & Joyce (2007), that pluripotential mesenchymal cells differentiate into osteoblasts, which in turn causes heterotopic ossification. Research has yet to determine the source of these mesenchymal cells and the stimulus that causes them to differentiate. So …show more content…

There are a few hereditary forms, fibrodysplasia ossificans progressive, which is a disorder in which muscle tissue and connective tissue such as tendons and ligaments are gradually replaced by bone, forming bone outside the skeleton. Another hereditary form of HO is progressive osseous heteroplasia, which is a disorder in which bone forms within skin and muscle tissue. Also, there is Albright’s hereditary osteodystrophy, which is completely different from the average HO. It is a syndrome with symptoms such as, short stature, obesity, round face, subcutaneous ossifications and characteristic shortening and widening of the bones in the hands and feet.
The most common symptom of heterotopic ossification according to Cluett (2014), is stiffness of a joint. Most people who develop heterotopic ossification cannot feel the abnormal bone, but notice the bone growth getting in the way of normal movements, which will cause loss in range of motion in the particular joint affected. HO forms around the hip or elbow joints, making bending of these joints difficult. Other symptoms may include a mass that can be felt, deformity of the area, pain along with localized swelling, and increase in the patient’s …show more content…

It can be difficult to distinguish from cellulitis, osteomyelitis, or thrombophlebitis. Bone scanning and other imaging tests frequently are used to distinguish between these diagnostic possibilities. It is difficult to differentiate early Heterotopic Ossification from deep venous thrombosis, because the symptoms may be similar. CT’s and radiography are also used to help diagnose Heterotopic Ossification. In early stages of HO it is hard to detect with CT and radiography, because HO is not detected on radiographs until 4-6 weeks post-injury. Further testing generally reveals an increase in serum alkaline phosphatase, a positive three-phase bone scan, and the identification of bone formation on radiographs. According to Bossche and Vanderstraeten (2005), four weeks post injury alkaline phosphate levels may reach 3.5 times the normal value, with a peak concentration around the 12th week. If Heterotopic Ossification formation is small, alkaline phosphate levels may remain unchanged. Alkaline phosphate levels are tested in the follow-up of

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