Skip to main content

Legg–Calve–Perthes disease

 Legg–Calve–Perthes disease



Overview

Legg-Calve-Perthes (LEG-kahl-VAY-PER-tuz) disease is a childhood condition that occurs when blood supply to the ball part (femoral head) of the hip joint is temporarily interrupted and the bone begins to die.

This weakened bone gradually breaks apart and can lose its round shape. The body eventually restores blood supply to the ball, and the ball heals. But if the ball is no longer round after it heals, it can cause pain and stiffness. The complete process of bone death, fracture and renewal can take several years.

To keep the ball part of the joint as round as possible, doctors use a variety of treatments that keep it snug in the socket portion of the joint. The socket acts as a mold for the fragmented femoral head as it heals.

Symptoms

Symptoms of Perthes disease include:

Limping.

Pain or stiffness in the hip, groin, thigh or knee.

Limited range of motion of the hip joint.

Pain that worsens with activity and improves with rest.

Perthes disease usually involves just one hip. Both hips can be affected, but they usually are affected at different times.

Causes

Perthes disease occurs when too little blood reaches the ball portion of the hip joint for a short time. Without enough blood, this bone becomes weak and collapses. The cause of the reduced blood flow is unknown.

Risk factors

Risk factors for Perthes disease include:

Age. Perthes disease can affect children of nearly any age, but it most commonly begins between ages 4 and 10.

Your child's sex. Perthes is about four times more common in boys than in girls.

Complications

Children who have had Perthes disease are at higher risk of developing hip arthritis in adulthood — especially if the hip joint has poor healing. If the ball-and-socket joint doesn't fit together well after healing, the joint can wear out early.

In general, children who are diagnosed with Perthes disease after age 6 are more likely to develop hip conditions later in life. The younger the child is at the time of diagnosis, the better the chances for the hip joint to heal in a typical, round shape.

Diagnosis

During the physical exam, your healthcare professional might move your child's legs into various positions to check range of motion and see whether any of the positions cause pain.

Imaging tests

These types of tests, which are vital to the diagnosis of Perthes disease, might include:

X-rays. Initial X-rays may not show changes in the hip. It can take 1 to 2 months after symptoms begin for the changes related to Perthes disease to become clear on X-rays. Your healthcare professional will likely recommend several X-rays over time to track the progression of the disease.

MRI. This technology uses radio waves and a strong magnetic field to make very detailed images of bone and soft tissue inside the body. MRIs often can visualize bone damage caused by Perthes disease more clearly than X-rays can, but MRI isn't always needed.

Treatment

In Perthes disease, the complete healing process can take several years. The types of treatment recommended depend on the:

Age when symptoms began.

Stage of the disease.

Amount of hip damage.

As Perthes disease gets worse, the ball part of the joint, called the femoral head, weakens and breaks apart. During healing, the socket part of the joint can serve as a mold. This can help the weakened femoral head keep its round shape.

For this molding to work, the femoral head must sit snugly within the socket. Sometimes a child wears a special type of leg cast that spreads the legs widely apart for 4 to 6 weeks to keep the bone in the right position.

Some children need surgery to help keep the ball of the joint snug within the socket. This procedure might involve making wedge-shaped cuts in the thighbone or pelvis to align the joint again.

Surgery generally isn't needed for children younger than 6. In this age group, the hip socket is naturally more moldable, so the ball and socket usually continue to fit together well without surgery.

Other treatments

Some children, especially very young ones, might need only conservative treatments or observation. Conservative treatments can include:

Activity restrictions. Children with Perthes disease should not run, jump or take part in other high-impact activities that might speed up hip damage.

Crutches. Sometimes, your child may need to avoid bearing weight on the affected hip. Using crutches can help protect the joint.

Physical therapy. As the hip stiffens, the muscles and ligaments around it may shorten. Stretching exercises can help keep the hip more flexible.

Anti-inflammatory medicines. Your healthcare professional might recommend infants' or children's medicines that you can buy without a prescription, such as ibuprofen (Advil, Motrin, others) to help relieve your child's pain.

Type of Doctor Department : A pediatric orthopedic surgeon or specialist

Comments

Popular posts from this blog

Charge Syndrome

Overview CHARGE syndrome is a recognizable genetic syndrome with known pattern of features. It is an extremely complex syndrome, involving extensive medical and physical difficulties that differ from child to child. CHARGE syndrome is correlated with genetic mutation to CHD7 and the prevalence of CHARGE syndrome is 1:10,000-1:15,000 live births. Babies with CHARGE syndrome are often born with life-threatening birth defects. They spend many months in the hospital and undergo many surgeries and other treatments. Swallowing and breathing problems make life difficult even when they come home. Most have hearing two little girls sitting on a carpet, one girl has a trach and is biting her finger.loss, vision loss, and balance problems that delay their development and communication. Despite these seemingly insurmountable obstacles, children with CHARGE syndrome often far surpass their medical, physical, educational, and social expectations. One of the hidden features of CHARGE syndrome is the ...

HMSN Type I

 HMSN Type I Overview Hereditary motor and sensory neuropathy type 1 (HMSN I), also known as Charcot-Marie-Tooth disease type 1 (CMT1), is a group of inherited neurological disorders affecting the peripheral nerves. It is characterized by progressive muscle weakness and wasting, primarily in the feet and legs, as well as sensory loss. HMSN I is the most common form of HMSN and is typically caused by a duplication on chromosome 17p11.2-p12, including the PMP22 gene.  Symptoms Numbness and tingling: Often starting in the feet and potentially extending to the hands, these sensations can mimic poor circulation.  Reduced ability to feel pain and temperature: This can lead to unnoticed injuries and complications.  Motor Symptoms: Muscle weakness and wasting: Primarily affecting the distal muscles (those farthest from the body's core), such as the feet and hands.  Foot deformities: High arches (pes cavus) and hammer toes are frequently observed.  Gait abnormalit...

Sjogren's syndrome

Sjogren's syndrome Overview Sjogren's (SHOW-grins) syndrome is a disorder of your immune system identified by its two most common symptoms — dry eyes and a dry mouth. The condition often accompanies other immune system disorders, such as rheumatoid arthritis and lupus. In Sjogren's syndrome, the mucous membranes and moisture-secreting glands of your eyes and mouth are usually affected first — resulting in decreased tears and saliva. Although you can develop Sjogren's syndrome at any age, most people are older than 40 at the time of diagnosis. The condition is much more common in women. Treatment focuses on relieving symptoms. Symptoms The two main symptoms of Sjogren's syndrome are: Dry eyes . Your eyes might burn, itch or feel gritty — as if there's sand in them. Dry mouth. Your mouth might feel like it's full of cotton, making it difficult to swallow or speak. Some people with Sjogren's syndrome also have one or more of the following: Joint pain, swel...