Myositis ossificans progressiva, forearm
ICD-10 M61.13 is a billable code used to indicate a diagnosis of myositis ossificans progressiva, forearm.
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 forearm and other areas of the body. Patients may experience muscle weakness, stiffness, and limited range of motion as the condition progresses. The ossification process can lead to significant functional impairment, as the affected muscles become increasingly replaced by bone. Diagnosis is often confirmed through imaging studies, such as X-rays or MRI, which reveal the presence of heterotopic ossification. Management of MOP is primarily supportive, focusing on physical therapy and pain management, as surgical intervention is often complicated by the risk of further ossification. Understanding the clinical presentation and progression of myositis ossificans progressiva is crucial for accurate coding and effective patient management.
Detailed history of symptoms, physical examination findings, and imaging results.
Patients presenting with unexplained muscle stiffness and swelling after trauma.
Documentation should emphasize the genetic nature of the condition and any family history.
Surgical notes, imaging studies, and post-operative assessments.
Patients requiring surgical intervention for severe ossification.
Careful documentation of the risks associated with surgery in patients with MOP.
Used when joint aspiration is needed due to swelling from ossification.
Document the reason for aspiration and findings during the procedure.
Orthopedic specialists should ensure clear documentation of the condition's impact on joint function.
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 typically made through clinical evaluation and imaging studies, such as X-rays or MRI, which reveal heterotopic ossification.
Treatment is primarily supportive, focusing on physical therapy and pain management, as surgical options carry risks of further ossification.
