What is osteochondritis dissecans?
Osteochondritis dissecans (OCD) is a term used to describe bone and cartilage injuries. If your child has OCD, a portion of his bone or cartilage has partially or completely separated from the surface of the joint. That's how the condition got its name: osteo (bone), chondrus (cartilage), itis (inflammation) and dissecans (to separate).
OCD most often affects the knee, but the elbow and ankle can also be affected. Lesions have been reported in other parts of the body, too.
While the exact cause of osteochondritis dissecans is unknown, several factors appear to play a role in determining which children may be affected.
OCD may stem from:
- Repetitive use and trauma of the affected joint
- Slightly decreased blood supply in some locations
- Other genetic factors
Signs and symptoms
Symptoms of osteochondritis dissecans can vary from child to child, and can change in intensity within one child with the disorder.
The most common symptoms of OCD include:
- Pain and swelling
- Locking or "catching" of the affected joint or area of the body
- Increased pain with activity
- A "giving way" sensation in the affected area
Testing and diagnosis
At Children's Hospital of Philadelphia (CHOP), OCD is treated by orthopaedic and sports medicine physicians who specialize in diagnosing and treating bone and muscle injuries in children, teens and young adults.
The first step in treating OCD is to modify your child's activities. Your child may need to temporarily change his sport or stop all activity in it.
Our multidisciplinary team will design a customized treatment program for your child that may include non-surgical options such as:
- Hard or soft cast to immobilize the bone/joint
- Weight-bearing or protected weight-bearing exercises
If non-operative treatment doesn't produce the desired effect — easing pain and allowing the bone to heal — surgical intervention may be necessary.
If surgery is needed, our world-renowned orthopaedic surgeons will:
- Secure or remove a loose piece of the bone
- Stimulate new bone formation
Your child with OCD should continue to be monitored periodically by a physician.
If your child had surgery, he will need to see the orthopaedic surgeon about one to two weeks after surgery, then again at three and six months post-surgery. After that, annual monitoring by trained clinicians is strongly encouraged to ensure any problems are spotted and treated as soon as possible.
During follow-up visits, X-rays and other diagnostic testing may be done. The goal of continued monitoring is to help spot any irregularities in growth or development and to address health issues as they develop.
Follow-up care and ongoing support and services are available at our Main Campus and throughout our CHOP Care Network. Our team is committed to partnering with parents and referring physicians to provide the most current, comprehensive and specialized care possible for your child.