Myositis ossificans progressiva, right ankle
ICD-10 M61.171 is a billable code used to indicate a diagnosis of myositis ossificans progressiva, right ankle.
Myositis ossificans progressiva (MOP) is a rare genetic disorder characterized by the abnormal formation of bone in muscles and connective tissues. This condition typically manifests after trauma or injury, leading to progressive ossification of soft tissues, particularly in the limbs. In the case of M61.171, the ossification occurs specifically in the right ankle region. Patients may experience muscle weakness, stiffness, and limited range of motion due to the formation of bone where muscle tissue should be. The condition is often misdiagnosed as other musculoskeletal disorders, which can complicate treatment. Diagnosis is primarily clinical, supported by imaging studies such as X-rays or MRIs that reveal the characteristic calcifications. Management focuses on symptomatic relief and physical therapy, but surgical intervention may be necessary in severe cases to remove excess bone formation. Understanding the nuances of this condition is crucial for accurate coding and appropriate patient management.
Detailed clinical notes on symptoms, physical examination findings, and imaging studies.
Patients presenting with unexplained muscle stiffness and swelling after trauma.
Ensure that genetic counseling and testing results are documented when applicable.
Surgical notes if intervention is performed, including pre-operative and post-operative assessments.
Patients requiring surgical intervention for severe ossification affecting mobility.
Document the extent of ossification and its impact on function.
Used for symptomatic relief in patients with joint swelling due to myositis ossificans.
Document the reason for the procedure, including clinical findings and imaging results.
Orthopedic specialists should ensure that the procedure is justified based on the patient's symptoms.
Myositis ossificans progressiva is a rare genetic disorder characterized by the abnormal formation of bone in muscles and connective tissues, often following trauma.
Diagnosis is primarily clinical, supported by imaging studies such as X-rays or MRIs that reveal characteristic calcifications in the affected area.
Treatment focuses on managing symptoms, including physical therapy and pain management, with surgical intervention considered in severe cases.
