Imaging provides answers in childhood back pain


Back pain is less common in children than in adults, but it may denote serious underlying disease in the pediatric age group and thus requires careful and thorough clinical, imaging, and laboratory-based investigation.

Back pain is less common in children than in adults, but it may denote serious underlying disease in the pediatric age group and thus requires careful and thorough clinical, imaging, and laboratory-based investigation. The causes of back pain in younger patients are various (see table), and knowledge of these may help when correlating symptoms to imaging findings.

Children tend to have significant elasticity in their spinal column. This increases the incidence of cord injuries without accompanying bone or joint injury.1 Most injuries are mild, resulting in bone marrow contusion or strains to the ligament or muscle. Injury commonly results in straight back syndrome caused by muscle spasm. Vertebral body fractures and dislocations are infrequent.2

Disc herniation in adolescents is more often traumatic than degenerative.2,3 Traumatic spondylolysis is usually induced in young, athletic adolescents by repetitive microtrauma,2,4 most commonly affecting level L5.5 Initial x-rays may be normal, reflecting the tendency of spondylolysis to start as a stress phenomenon and progress later into a fracture. SPECT is highly sensitive to the detection of early stress injuries, and normal scans will exclude pars injuries.6 CT has a higher sensitivity than radiography in detecting pars fractures. Pars edema seen on MRI denotes a stress phenomenon (Figure 1). Ring apophyseal fracture of the posterior vertebral endplate most commonly involves the inferior rim of L4.7

Disc degeneration may develop during growth either with or without prolapse.2 Diagnosis is best made by MRI, which will show low signal intensity on T2-weighted images. Spondylolisthesis without spondylolysis may be caused by congenital deficiency of the facet joints. It can also be the result of elongated pars interarticularis, due to either congenital malformation or repetitive microfractures.8 Diagnosis is made by plain-film x-ray and CT.

Scoliosis may be idiopathic, congenital, or due to variable disease processes. Most cases are idiopathic and painless. Painful scoliosis is usually secondary to a vertebral or rib lesion. Congenital scoliosis may be classified as a defect of formation and/or segmentation.

Scheuermann's disease, a condition affecting adolescents and young adults (under the age of 18) is related to repetitive trauma. It is characterized by vertebral wedging, endplate irregularity, disc space narrowing (with or without disc protrusion, Figure 2), and intravertebral disc herniation (Schmorl's nodes).2 Thoracic kyphosis will increase, and both the thoracic and lumbar spine may be affected. Lumbar involvement appears to be more painful.


Spinal involvement, or tuberculous spondylodiscitis, is seen in 15% of tuberculosis patients. Clinical presentation is insidious. Involvement consists of a hematogenous and subligamentous spread. It often results in soft-tissue abscesses, osteitis, or discitis. More than one vertebral body is usually involved in contiguous manner, mainly at the thoracolumbar junction.

Plain-film x-ray and CT will both show bone destruction, sclerosis, or disc space narrowing. Spinal deformity and/or fusion occur later. MRI is the best modality to show the extent of spinal involvement, although MR signals from spinal infection in children are different from those seen in adults. The normal vertebra is visualized as low signal on T1-weighted images, due to red bone marrow, while the disc appears as high signal on T2-weighted MRI. In tuberculosis, however, disc involvement shows low signal intensity on T2-weighted imaging.9 Vertebral involvement is best seen following gadolinium injection, which causes the vertebrae to enhance.

Nontuberculous spondylodiscitis may be unspecific (nonpyogenic, traumatic) or infectious (bacterial). The spine becomes involved by hematogenous spread or from an infected contiguous source. Radiographs show disc space narrowing, decreased vertebral height, and irregular endplates. Kyphosis, scoliosis, and sclerotic changes can occur in the later stages. Signal intensity on MRI is similar to that seen in tuberculous spondylitis.

Juvenile seronegative spondyloarthropathies are the most common inflammatory disorders affecting the pediatric spine. They are a late manifestation that follows sacroiliitis. Juvenile rheumatoid arthritis rarely affects the spine and seldom causes back pain.


Osteoid osteoma is a common benign bone-forming tumor that consists of a central core of vascular connective tissue and osteoid nidus (usually 1 to 2 cm), with reactive sclerosis of the surrounding bone. The nidus shows calcifications as it matures.10 Spinal osteoid osteoma, which occurs in 10% to 18% of all cases, involves posterior elements in the main (Figure 3). Dense sclerotic areas obscuring the nidus that can be seen on x-ray are usually at the concave side of painful scoliosis. A CT scan can accurately localize the nidus in most cases. The nidus is frequently calcified and easy to diagnose by CT. When the nidus is not calcified, a CT scan would still be very sensitive in detecting it, but the specificity of the diagnosis will depend on the presence of the surrounding sclerosis that is usually seen in osteoid osteoma. MRI shows bone marrow and overlying soft-tissue edema. The nidus may be visualized on a gadolinium-enhanced study.

Osteoblastoma has a histopathology similar to osteoid osteoma,10 but it is larger in size and may be aggressive. One-third of all osteoblastomas occur in the spine, and nearly all of them involve posterior elements.10 Radiography and CT typically show a lytic expansile lesion with varying degrees of mineralization. Surrounding bone sclerosis is rare.

The aneurysmal bone cyst is a benign cystic bone lesion, which may either be a true primary tumor or develop within a preexisting lesion. The spine is involved in 11% of cases, occurring more at the lumbar level.2 Posterior elements are always involved, with infrequent extension to vertebral bodies.2 Radiography and CT reveal a well-defined lytic expansile lesion with internal trabeculae and septae. Fluid-fluid levels and enhancing septae are seen frequently on MRI. Angiography is performed if presurgical embolization is planned.

Leukemia is usually encountered in childhood and adolescence, and acute forms represent more than one-third of pediatric malignancies.11 Radiography shows a generalized decrease in bone density, which may cause compression fractures.

Osteosarcoma is the most common malignant bone tumor in children and young adults.10 It involves the vertebral column in 4% of cases, mainly the posterior elements (79%). Osteosarcoma is seen as destructive, with variable degrees of mineralization, on radiography and CT. The tumor has no specific features on MRI.

Ewing's sarcoma is the second most common malignant bone tumor in children.10 The tumor typically involves the vertebral body in the spine (Figure 4). Neurological signs may be seen as well as back pain, due to intraspinal extension. Radiographic and CT findings include a mixture of destructive and sclerotic behavior. Findings are unspecific on MRI.

Langerhans cell histiocytosis is an uncommon disease caused by infiltration of various tissues by a unique type of histiocytes, the Langerhans cell. It may present in three main forms. Vertebral bodies are commonly involved when Langerhans cell histiocytosis affects the spine. This involvement is frequently multifocal10 but rarely includes posterior elements.12 Degrees of collapse are variable. Epidural extension is seen in 15% of cases.

Spinal involvement in lymphoma is due to hematogenous spread or direct invasion. It is more commonly encountered in non-Hodgkin's lymphoma than in Hodgkin's disease.13 Radiography and CT usually demonstrate destructive lesions. Lesions have low signal intensity on T1-weighted MRI and variable signal on T2-weighted images.

Many different types of metastases can occur in the spine. They can be lytic, blastic, or mixed, depending on the primary lesion. MRI is the best modality to detect and assess the extent of metastatic disease in the spine.


Sickle cell disease can result in either infarction or infection when congested cellular marrow impedes blood flow. Infarctions produce an H-shaped vertebral deformity. These are seen as low signal intensity on T1-weighted MRI and variable signal on T2-weighted imaging.

Primary osteoporosis in childhood is very rare. When it does occur, it is usually caused by osteogenesis imperfecta or idiopathic juvenile osteoporosis. Secondary osteoporosis is more common because it can be caused by a large number of chronic pediatric diseases and also by therapeutic regimens used to treat these diseases, which include some drugs and radiation therapy, as in lymphoma treatment. Childhood osteoporosis is usually asymptomatic but may be discovered after light trauma leading to vertebral fracture (44%). The diagnosis can be confirmed by bone densitometry.

Alkaptonuria is an autosomal recessive genetic disorder caused by deficiency of the homogentisate dioxygenase.1,2 This results in the accumulation of homogentisic acid and its metabolites in different structures of the body. Several abnormalities are encountered in the spine, including disc space narrowing and calcification of the interosseous ligaments.14 Increased kyphosis is common.

Osteopetrosis is a rare skeletal disease caused by aberrant bone resorption that is characterized by increased bone density. Three clinical forms are known: infantile autosomal recessive osteopetrosis, intermediate autosomal recessive osteopetrosis, and adult autosomal dominant osteopetrosis (Albers-Schonberg disease). Back pain may be present either with or without underlying fracture.15 A variable degree of osteosclerosis is seen on imaging. Accentuation of the vertebral endplates ("sandwich" appearance) and the more typical "bone within bone" appearance will also be seen.

In conclusion, a wide range of benign and malignant disorders can cause back pain in children and adolescents. Clinicians and radiologists should be aware of these conditions so that appropriate imaging studies can be ordered and delays in diagnosis and management kept to a minimum.


Mechanical or sports injury
Discogenic herniation
Traumatic spondylolysis andsecondary spondylolisthesis
Ring apophyseal fracture

Diseases related to growth disturbance
Disc degeneration
Spondylolisthesis without
spondylolysis scoliosis
Scheuermann's disease

Inflammatory spondyloarthropathy

Neoplastic disorders, benign
Osteoid osteoma
Aneurysmal bone cyst

Neoplastic disorders, malignant
Ewing's sarcoma
Langerhans cell histiocytosis

Hematological disorders
Sickle cell disease

Metabolic disorders


DR. ARABI is chief resident, DR. KHOURY is an assistant professor, and DR. HOURANI is an associate professor, all in the department of diagnostic radiology at the American University of Beirut Medical Center in Lebanon. Assisting in the preparation of this manuscript were Dr. Faysal Abu Fakhr and Dr. Maurice Haddad in the same department.

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11. Parker BR. Leukemia and lymphoma in childhood. Radiol Clin N Am 1997;35(6):1495-1516.
12. Meyer J, Harty MP, Mahboubi S, et al. Langerhans cell histiocytosis: presentation and evolution of radiologic findings with clinical correlation. Radiographics 1995;15(5):1135-1146.
13. Krishnan A, Shirkhoda A, Tehranzadeh J, et al. Primary bone lymphoma: radiographic-MR imaging correlation. Radiographics 2003;23(6):1371-1387.
14. Taybi H. Metabolic disorders. In: Taybi H, Lachman RS, ed. Radiology of syndromes, metabolic dysplasias and skeletal dysplasias. St. Louis: Mosby, 1996:550-551.
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