Inflammatory fibrous hyperplasia; Idiopathic fibrous hyperplasia
Fibrous dysplasia is a bone disease that destroys and replaces normal bone with fibrous bone tissue. One or more bones can be affected.
Fibrous dysplasia occurs in childhood, usually between ages 3 and 15. The condition is linked to a problem with genes (gene mutation) that control bone-producing cells. The mutation occurs when a baby is developing in the womb. The condition is not passed from parent to child.
Symptoms may include any of the following:
The bone lesions may stop when the child reaches puberty.
The doctor will perform a physical examination. X-rays of bones are taken.
There is no cure for fibrous dysplasia. Bone fractures or deformities are treated as needed. Hormone problems will need to be treated.
The outlook depends on the severity of the condition and the symptoms that occur.
Depending on the bones that are affected, health problems that may result include:
Call your health care provider if your child has symptoms of this condition, such as repeated bone fractures and unexplained bone deformity.
Specialists in orthopedics, endocrinology, and genetics may be involved in your child's diagnosis and care.
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.
Blanco P, Wientroub S. Fibrous dysplasia. In: Glorieus FH, Perrifor JM, Juppner H, eds. Pediatric Bone. 2nd ed. Philadelphia, PA: Elsevier; 2012:chap 22.
Czerniak B. Fibrous dysplasia and related lesions. In: Czerniak B, ed. Bone Tumors. 2nd ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 8.
Last reviewed on: 11/19/2015
Reviewed by: Neil K. Kaneshiro, MD, MHA, Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine, Seattle, WA. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.