Myositis ossificans progressiva, left upper arm
ICD-10 M61.122 is a billable code used to indicate a diagnosis of myositis ossificans progressiva, left upper arm.
Myositis ossificans progressiva (MOP) is a rare genetic disorder characterized by the abnormal formation of bone in muscles, tendons, and other connective tissues. This condition typically presents with progressive muscle stiffness and weakness, often following minor trauma or injury. In the case of M61.122, the ossification occurs specifically in the left upper arm, leading to significant functional impairment. Patients may experience pain, swelling, and a decrease in range of motion as the condition progresses. The ossification process can lead to the formation of heterotopic bone, which can severely restrict mobility and quality of life. Diagnosis is often confirmed through imaging studies such as X-rays or MRI, which reveal the presence of abnormal bone formation. Management of MOP is primarily supportive, focusing on pain relief and maintaining mobility, as surgical intervention is often complicated by the risk of further ossification. Understanding the nuances of this condition is crucial for accurate coding and appropriate patient management.
Detailed clinical notes on symptoms, progression, and treatment response.
Patients presenting with unexplained muscle stiffness and pain after minor trauma.
Documentation should include family history and genetic testing results if applicable.
Surgical notes if intervention is performed, including pre-operative assessments.
Patients requiring surgical evaluation for restricted mobility due to ossification.
Careful documentation of the risks associated with surgery in patients with MOP.
Used for pain management in patients with MOP experiencing joint swelling.
Document the reason for the procedure and any imaging studies performed.
Orthopedic specialists should ensure clear documentation of the patient's condition and treatment plan.
Myositis ossificans progressiva is a rare genetic disorder characterized by the abnormal formation of bone in soft tissues, leading to progressive stiffness and weakness.
Diagnosis is typically made through clinical evaluation, imaging studies such as X-rays or MRI, and consideration of the patient's history.
Treatment is primarily supportive, focusing on pain management and maintaining mobility, as surgical options carry risks of further ossification.
