McCune-Albright’s Polyostotic Fibrous Dysplasia


I would like to receive information about “fibrous dysplasia,” also known as the McCune-Albright syndrome. Especially about the prospects.
Ingrid van Steen – Tilburg- The Netherlands

Dr. Greene's Answer

Two years ago, I first saw an otherwise healthy 9-year-old boy named Dennis. He had come to see me for a sore throat, but during the examination I noticed that he had an unusual birthmark. It was on his chest: large, light brown, with irregularly jagged borders. It stopped abruptly at the midline of his chest. On further examination I discovered that he had a notably large penis and testicles. Dennis had a rare condition called McCune-Albright’s polyostotic fibrous dysplasia.

This condition was first described by McCune and Albright in 1936 and 1937 respectively. They described the classic triad of irregular skin pigmentation, bony abnormalities, and sexual precocity.

The skin pigmentation, seen in approximately 50% of McCune-Albright patients, is often present in infancy, and is thus frequently the first sign. The characteristic lesions are called cafe au lait spots — large, flat, light brown spots. The McCune-Albright spots are distinguished by the serrated borders (called “coast of Maine”) and by their tendency to stop abruptly at the midline of the body. Many other children have cafe au lait spots, but normally they have smooth (“coast of California”) borders.

The bony abnormalities are called polyostotic fibrous dysplasia, or ineffective growth in multiple bones. On x-ray this is seen as patchy areas of osteoporosis and areas of bone thickening. This may result in repeated fractures or even skeletal deformity, most commonly in the upper femur (large bone of the thigh). The fibrous dysplasia usually progresses throughout childhood. The cafe au lait spots tend to overly the areas of most bony involvement. Rarely, thickening of the skull bone can compress cranial nerves, causing blindness or deafness if untreated.

The third piece of the classic triad, precocious puberty, is most often seen in girls. When sexual precocity is present, menstruation usually begins prior to development of breasts or pubic hair. The average age for the first period is three. Boys begin with enlargement of the testicles, followed quickly by enlargement of the penis and the development of pubic hair.

McCune-Albright syndrome is unique among all genetic diseases. Some genetic diseases have dominant inheritance, some recessive. Some diseases have sex-linked inheritance, some result from too many or too few chromosomes. Some diseases are polygenic or multifactorial, inherited through changes on several genes. Could there be genetic diseases that are never inherited? So far, only one has been discovered — McCune-Albright syndrome!

How could this be?

When all the cells in a person do not have the same genetic make up, that person is called a mosaic. At some point early in development, one cell mutates. All of its progeny will have the same DNA code — but different from the rest of the body. The timing in development when this mutation occurs will determine what proportions of the body have the two different types of DNA. All of us are mosaics to some degree. Mosaicism is the basis for most (if not all) birthmarks. It is the basis for moles and freckles. It is also the basis for tumors.

For the first four decades after McCune-Albright syndrome was described, it was defined simply as people who shared in common the triad of characteristics described above. In the last decade, the gene coding for McCune-Albright has been found. It codes for the G protein that stimulates an important body signal called cAMP, which regulates many of the hormone-producing glands in the body.

No fertilized egg that had this defect could survive.

McCune-Albright cannot be inherited; it can only appear as a mosaic. Because this mutation occurs in different tissues in different people, the clinical condition varies widely. It is now known that the McCune-Albright defect can cause abnormalities in many of the body’s hormone systems. Some develop hyperthyroidism, some over-stimulation of the adrenal glands. A number of patients have increased growth hormone, and they can grow to be quite tall. Others end up quite short from ending puberty too early. Hormonal changes also underlie many (if not all) of the bony problems encountered.

All patients with McCune-Albright syndrome must be thoroughly investigated. Each is unique. Specific treatments are quite effective for imbalances in each of the affected systems — if the imbalances are discovered. However, once the bony lesions have appeared, deformities, repeated fractures, and pain are not uncommon.

Properly treated, the prognosis for people with McCune-Albright syndrome is excellent for longevity and intelligence. Unfortunately, Dennis’s parents didn’t believe their son could have a rare disease. After his first visit they never returned; I have been unable to locate them.

Last medical review on: July 30, 2008
About the Author
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Dr. Greene is a practicing physician, author, national and international TEDx speaker, and global health advocate. He is a graduate of Princeton University and University of California San Francisco.
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Recent Comments

Thank you kindly for responding. As a side note, I wonder if this syndrome is tied in with PCOS?

Although it is described as mosaic gene mutation, non inheritable disorder, I wonder about a genetic link in some of its variances? I had accelerated growth as a child, likely central idiopathic precocious puberty. Both my daughters (now 22 and 24) had diagnosis of precocious puberty from hand xray growth plates. Both my daughters are diagnoses with PCOS. Recently, I have ultra sounds showing peri-menopausal cysts. Although never officially diagnoses with PCOS, in hindsight, I may have it: I was pre-eclampsic during pregnancy and gave birth to large babies: I had terrible acne, and vaguely remember elevated hormone results (LH/FSH?) while in my twenties. All three of us struggle with weight issues–but my youngest daughter is the only one with cafe-au-lait

It just seems too co-incidental.

My daughter, she is now 22 years old had precocious puberty as per hand xray of growth plates at age 11. However she is of normal size. She has a large cafe-a-lait on her chest. She has frequent pain in limbs and prone to fractures. She was born with a atrial septal defect. She now is diagnosed with poly cystic ovarian disease. Also has migraines, and IBS. At age 8 she was diagnosed with tourettes syndrome. She had/has mild learning disabilities. Should be be tested for this syndrome?

My daughter (now 22 years old) had precocious puberty as per hand x-ray of growth plates at age 11. However she is of normal size. She has a large cafe-a-lait spot on her chest. She has frequent pain in limbs and is prone to fractures. She was born with a atrial septal defect.

She now is diagnosed with poly cystic ovarian disease. Also has migraines, and IBS. At age 8 she was diagnosed with tourettes syndrome. She had/has mild learning disabilities. Should she be tested for this syndrome?

It sounds like you and your daughter have been through a lot. Whenever someone has multiple unrelated issues like those you mentioned, I’m a fan of being evaluated by a medical geneticist to see if there might be a rare condition that ties them all together. That’s often how syndromes like this one are uncovered in people.