Understanding a Fibrous Dysplasia Diagnosis
Fibrous dysplasia is a rare bone disorder that causes scar-like tissue to develop in the bone, weakening it and potentially causing deformities or fractures. In most cases, a single bone is affected — often the skull. The condition is considered genetic because it occurs during a baby’s development before birth, but it is not hereditary. Symptoms often don’t show until adolescence or young adulthood.
Fibrous dysplasia is linked to birthmarks (cafe-au-lait spots); endocrine problems, including premature puberty; hyperthyroidism; low blood phosphorus; secretion of excess growth hormone, and, very rarely, neonatal Cushing’s disease. There is no cure, but fibrous dysplasia can be managed with surgery.
The AdventHealth Neuroscience Institute network specializes in minimally invasive treatments that use laser technology to remove affected tissue in the bone. These advanced techniques often minimize damage to surrounding tissue and result in less scarring and pain. Using image-guided stereotactic neurosurgery, our specialists can view 3D images of fibrous tissue during surgery, making it easier to remove. Minimally invasive surgery helps manage symptoms, including pain, and results in quicker recovery because no incision is made.
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