What Doctor Treats Fibrous Dysplasia?


There is no known way to prevent fibrous dysplasia. Treatment aims to prevent complications, such as recurrent bone fractures, to help make the condition less severe.

How many people does fibrous dysplasia affect?

Fibrous dysplasia (FD) is one of those conditions. With an estimated prevalence of 1 in 15000-30000 individuals , it is unsurprising that I had never come across it.

How do you get rid of fibrous dysplasia?

Unfortunately, there is no cure for fibrous dysplasia; however, treatments may help to relieve pain, and supportive measures such as physical therapy may help strengthen muscle and improve range of motion.

Does fibrous dysplasia affect teeth?

Teeth may become displaced as the lesion grows, while the arch form typically maintains its characteristic shape (Figure 3B). Radiographically, the characteristic “ground glass” appearance, of mixed radiolucency/opacity, may be seen – this is a result of woven or abnormal bone superimposed on a fibrous tissue matrix.

What does fibrous dysplasia feel like?

As fibrous bone tissue grows and expands, the affected area can become weak and painful. Pain is more likely to occur if the bone affected is one of the weight-bearing bones of the leg or pelvis. Pain caused by fibrous dysplasia generally begins as a dull ache that worsens with activity and lessens with rest.

Can fibrous dysplasia be cured?

Although fibrous dysplasia is a genetic disorder, it’s caused by a gene mutation that’s not passed from parent to child. There’s no cure for the disorder. Treatment, which may include surgery, focuses on relieving pain and repairing or stabilizing bones.

Is fibrous dysplasia a rare disease?

Fibrous dysplasia (FD) is a rare bone disorder. Bone affected by this disorder is replaced by abnormal scar-like (fibrous) connective tissue. This abnormal fibrous tissue weakens the bone, making it abnormally fragile and prone to fracture. Pain may occur in the affected areas.

What causes fibrodysplasia?

FOP is caused by the mutation of a gene (ACVR1) in the bone morphogenetic protein (BMP) pathway, which is important during the formation of the skeleton in the embryo and the repair of the skeleton following birth.

Who is affected by fibrous dysplasia?

Fibrous dysplasia usually occurs in children ages 3 to 15. It is sometimes not diagnosed until adulthood. It is found equally in men and women.

What are the symptoms of fibrous?

What are the symptoms of fibrous dysplasia?

  • A waddling walk.
  • Bone deformity.
  • Bone fractures.
  • Bone pain (which happens when the fibrous tissue expands in the bone)
  • Scoliosis (a sideways curve of the spine)
  • Hormonal disturbances.
  • Skin discoloration.

Can fibrous dysplasia invade soft tissue?

Fibrous dysplasia generally stops growing when patients reach adulthood. Locally aggressive fibrous dysplasia is an extremely rare subtype of fibrous dysplasia that is characterized by progressive enlargement after bone maturation, cortical bone destruction and soft tissue invasion but without malignant transformation.

How do you diagnose fibrous dysplasia?

The primary tool for diagnosis of fibrous dysplasia is an X-ray. While bone appears solid in an X-ray, a fibrous dysplasia lesion has a relative distinct appearance often described as “ground glass.” The condition may be diagnosed, therefore, even in a person with no symptoms who is getting an X-ray for other reasons.


What is the treatment for fibrodysplasia?

Unfortunately, there is no effective treatment for fibrodysplasia ossificans progressiva (FOP). Surgery is not an option for removing the excess bones because surgery often results in more bone formation. And these new bones don’t disappear on their own.

Does fibrous dysplasia cause headaches?

Fibrous dysplasia originating from the ethmoid bone is a rare disease entity, but may cause severe headache that can be misdiagnosed as “menstrual migraine” because of similar symptoms in female patients.

Does fibrous dysplasia affect bone marrow?

In fibrous dysplasia/McCune-Albright syndrome (FD/MAS), bone and bone marrow are, to varying degrees, replaced by fibro-osseous tissue typically devoid of hematopoietic marrow. Despite the extensive marrow replacement in severely affected patients, bone marrow failure is not commonly associated with FD/MAS.

Is Osteofibrous dysplasia genetic?

Osteofibrous dysplasia is a rare, genetic primary bone dysplasia characterized by the presence of a benign, fibro-osseous, osteolytic tumor typically located in the tibia (occasionally the fibula, or both) and usually involving the anterior diaphyseal cortex with adjacent cortical expansion.

What is the life expectancy of someone with FOP?

FOP can become severely disabling. Most people with FOP will need a wheelchair by the time they reach their late 20s. The median lifespan for people with FOP is 40 years .

Is fibrous dysplasia a tumor?

Background: Fibrous dysplasia is a benign fibroosseous bone tumor that accounts for 5% to 10% of benign bone tumors. It can present as monostotic fibrous dysplasia (70% to 80%), polyostotic fibrous dysplasia (20% to 30%), McCune-Albright syndrome (2% to 3%), or Mazabraud’s syndrome in rare cases.

What are the signs of dysplasia?

What are the signs and symptoms of hip dysplasia?

  • Pain in the hip.
  • Loose or unstable hip joint.
  • Limping when walking.
  • Unequal leg lengths.

What is craniofacial fibrous dysplasia?

Craniofacial fibrous dysplasia is a bone disease of the face and skull that replaces normal bone with fibrous-type tissue. This tissue is not as hard as normal bone, and because it is soft and stringy, it makes the bone more fragile and prone to break.

What is McCune Albright syndrome?

McCune-Albright syndrome is a disorder that affects the bones, skin, and several hormone-producing (endocrine) tissues. People with McCune-Albright syndrome develop areas of abnormal scar-like (fibrous) tissue in their bones, a condition called polyostotic fibrous dysplasia.

How does osteosarcoma differ from fibrous dysplasia?

Fibrous dysplasia is not associated with cortical destruction, except in cases that are associated with a pathologic fracture. In contrast, the majority of central low-grade osteosarcomas show some degree of cortical disruption with or without soft tissue extension.

What is cellular dysplasia?

A term used to describe the presence of abnormal cells within a tissue or organ. Dysplasia is not cancer, but it may sometimes become cancer. Dysplasia can be mild, moderate, or severe, depending on how abnormal the cells look under a microscope and how much of the tissue or organ is affected.