Myositis ossificans progressiva, right lower leg
ICD-10 M61.161 is a billable code used to indicate a diagnosis of myositis ossificans progressiva, right lower leg.
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 in childhood or early adulthood and is often triggered by trauma or injury, although it can occur spontaneously. In the case of M61.161, the ossification occurs specifically in the right lower leg, leading to progressive muscle stiffness, weakness, and reduced mobility. Patients may experience episodes of swelling and pain in the affected area, which can be mistaken for other conditions such as muscle strains or sprains. The ossification process can severely limit joint movement and function, leading to significant disability. Diagnosis is primarily clinical, supported by imaging studies such as X-rays or MRI, which reveal the presence of heterotopic bone formation. Genetic testing may also be utilized to confirm the diagnosis, particularly in atypical cases. Management focuses on symptomatic relief, physical therapy, and avoiding invasive procedures that may exacerbate the condition. Understanding the complexities of MOP is crucial for accurate coding and appropriate patient management.
Detailed clinical notes on physical examination, imaging results, and treatment plans.
Patients presenting with unexplained muscle stiffness and swelling after trauma.
Documentation must clearly outline the progression of symptoms and any interventions attempted.
Genetic testing results and family history documentation.
Patients with a family history of myositis ossificans or unexplained ossification.
Ensure that genetic counseling notes are included to support the diagnosis.
Used when imaging is required to assess for ossification in the lower leg.
Radiology reports must be included to support the diagnosis.
Orthopedic specialists should ensure imaging findings correlate with clinical symptoms.
Myositis ossificans progressiva is a rare genetic disorder characterized by the abnormal formation of bone in muscles and connective tissues, leading to progressive stiffness and weakness.
Diagnosis is primarily clinical, supported by imaging studies that reveal heterotopic ossification and may include genetic testing to confirm the condition.
