Scheuermann's Kyphosis
Original Editors - Liza De Dobbeleer
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Definition/Description[edit | edit source]
Scheuermann’s disease, also known as juvenile osteochondrosis, is named after Holger Werfel Scheuermann. The disease is characterized by a defect in shape of the spine with a curvature of the spine as result.[1] People who suffer with this disease have irregularities of the vertebral endplates, the presence of Schmorl's nodes, disk-space narrowing and vertebral wedging.[2] At each level of the lumbar vertebrae can prevent this abnormality, hence the name lumbar Scheuermann’s disease. The disease mostly develops during puberty and is seen equally in both sexes. Depending on which criteria is used, has 5 to 40% of the population this anomaly.[1] [3]
The skeleton of a newborn consists mainly of cartilage, which in childhood is almost completely transformed into bone.[3] The lumbar Scheuermann’s disease is related to defects in the ossification process. This is often located at the anterior of the lumbar vertebrae (usually the first lumbar vertebrae to the fourth). This is the reason why these patients exhibit an increased lordosis.
The disease can range from mild to a server life-threatening deformity. Some people have no problems (mild threatening) but others will experience problems such as increasing curved spine, pain, neurological problems and symptoms of heart or lung problems. Although there’s no real condition discovered, deserve some typically elements of the disease special attention of researchers. Some studies showed that there’s a genetic component, Ascani et al also proved that patients with the condition are often taller than others of similar age. Mostly, the patients have a greater lordosis in the lumbar spine than normal people.[4] [5]
In addition, it has been suggested that between 20 to 30% of patients with Scheuermann’s disease also have scoliosis. In more serious cases, the combination is sometimes known as kyphoscoliosis.
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