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Chapter 25 Back Pain in Children and Adolescents 423
sleep, and does not radiate. It is exacerbated by vigorous activ­ity and prolonged sitting. e severity of the back pain is variable, with some patients denying signicant symptoms
and instead presenting for evaluation of poor posture. Neuro­logic symptoms are highly unusual.
Physical examination of the patient with Scheuermann disease shows increased thoracic kyphosis, which is most notable on forward bending, in which the apex appears to protrude posteriorly. e deformity is usually fairly rigid, and
does not disappear with hyperextension. ere may be con­comitant hamstring tightness, with inability to touch the oor with the ngertips.
e diagnosis is made radiographically (Fig. 25.5). Criteria for the diagnosis of Scheuermann disease have been outlined by Sorenson as:
1. three contiguous vertebral bodies with greater than 5
degrees of anterior wedging
2. abnormal disc narrowing
3. endplate irregularities
4. Schmorl nodes, dened as disc herniations into the verte-
bral bodies
e vast majority of patients with Scheuermann disease can be managed nonoperatively.63 Physical therapy exercises and nonsteroidal medication can be helpful in relieving symptoms. e role of bracing is controversial. Patients with signicant
remaining spinal growth may benet from orthotic treatment because it has been proposed that correction of deformity may be achieved in compliant patients.64 e Milwaukee brace
is the orthosis of choice for the treatment of Scheuermann disease.65 Surgical correction of deformity and fusion is
reserved for patients with severe kyphosis measuring greater than 75 degrees, those whose symptoms are refractory to con­servative measures, and those who have signicant cosmetic
concerns.
66
Lumbar Scheuermann Disease
Lumbar Scheuermann disease is a less common variant in which increased kyphosis and endplate changes are seen in the lumbar spine.67 It also occurs most frequently in adolescence, with overuse believed to be the cause. Microfractures occur in the vertebral endplates, resulting in low back pain. Radio­graphs reveal endplate irregularities and disc space narrow­ing, anterior Schmorl nodes, and possible anterior wedging of the aected vertebrae, leading to loss of lumbar lordosis.
Radiographs may also show associated spondylolysis or sco-
27,68
liosis.
e radiographic appearance of vertebral changes and disc space narrowing may resemble infection or tumor. Scintigraphy may reveal mildly increased uptake at one or two vertebral levels.27 MRI shows signal change and dehydration in the lumbar discs, with further disc deterioration occurring over time.69 Treatment is symptomatic, and pain is usually ameliorated with modication of activity or use of an orthosis.
Idiopathic Scoliosis
e majority of patients who have idiopathic scoliosis do not complain of back pain, but symptoms are not as uncommon as previously thought. In a study by Ramirez and coworkers,23 32% of 2442 children believed to have idiopathic curves complained of some degree of back pain. e most common factor associated with a positive diagnosis on further evalua­tion were le-sided thoracic curves, which were associated
with spinal cord abnormalities. Plain radiographs were found to be sucient in the evaluation of typical curves if the neu­rologic examination was normal. Careful inspection of the apex of the deformity and at the lumbosacral junction (for spondylolysis and spondylolisthesis) will occasionally yield a cause for both the pain and the scoliosis (see Fig. 25.4). In the absence of neurologic ndings on physical examination, MRI
was not helpful. A recent study did show that MRI was useful in identifying neural axis abnormalities in 6% of 104 patients. Back pain and early age of onset of scoliosis were present in those with MRI abnormalities.
70
SECTION
IV
FIG. 25.5 Anterior wedging of the thoracic spine in a 15-year-old male
with Scheuermann kyphosis.
Syringomyelia
Syringomyelia is dened as cystic dilation of the central canal of the spinal cord. e dilation of the cord leads to abnormali-
ties in the neurologic pathways that transmit pain and tem­perature. While not always symptomatic, patients may complain of pain. ere is a predisposition toward le thoracic
scoliosis in patients with syringomyelia.71 Physical ndings include scoliosis, foot deformities such as cavus, decreased sensation, and asymmetric abdominal reexes. e syrinx is
clearly imaged on MRI. Treatment is neurosurgical decom­pression, although controversy exists regarding the size of syrinx that requires surgery.
424 PEDIATRICS
Tethered Spinal Cord
Low back pain may be the presenting complaint in children with tethered spinal cords. e cord normally terminates at
the L1–L2 level. Persistence of the cord more distally implies tethering. Physical ndings may include foot deformity, spas-
ticity, or weakness. Oen, radiographs will show coexistent congenital vertebral abnormalities. e diagnosis is made on
MRI, in which the lum may appear thickened or the conus visualized at L3 or distal. Treatment of the symptomatic tethered cord is surgical release, which is typically performed by a neurosurgeon.
Idiopathic Juvenile Osteoporosis
Idiopathic juvenile osteoporosis is a rare disease that usually aects children in the rst 2 decades of life. Presenting symp- toms include back and leg pain due to compression fractures and pain during weight bearing. include vertebral wedging due to compression fractures with mildly increased kyphosis. Bone mineral density is decreased, but metabolic laboratory values are normal. e dierential
diagnosis includes leukemia. Orthotic management of back pain is usually sucient. Medical management should be under the supervision of a pediatric rheumatologist. e disease is self-limiting, and symptoms resolve during puberty.
72,73
Radiographic ndings
74
FIG. 25.6 Disc space narrowing (arrow) and endplate irregularities in a
child with T11–T12 discitis.
Infectious and Inammatory Etiologies
Discitis
Discitis is dened as a presumed bacterial infection of the intervertebral disc space. It is the most common cause of back pain in the young child. e incidence of discitis is greatest
in children aged 5 years and younger, though it can occur in older children.75 e etiology is believed to be infectious. In the immature child, blood vessels traverse the vertebral end­plates and terminate in the nucleus pulposus. erefore, in young children the disc is vascular, which allows for seeding of bacteria into the disc space. but include back pain, refusal to walk, limping, and abdominal pain. e child usually is systemically ill; therefore, the patient oen presents to the emergency department. Approximately
half will have fever on presentation.
Physical examination reveals spinal stiness, and oen the
spine is held in a exed position. If asked to retrieve a toy from
the oor, the child with discitis will squat by bending the knees rather than bend the spine. Young children may exhibit Gower’s sign when rising from the oor, using their upper extremities to push up on the legs as a strategy to minimize lumbar motion. Tenderness in palpation of the aected area can be present.
Radiographic ndings are usually minimal at the time of
presentation. Subtle disc space narrowing and paraspinal so tissue swelling on the lateral view are the rst radiographic
changes (Fig. 25.6). Over time, endplate irregularities are seen. Because plain radiographs are usually normal at the time of presentation, further imaging is required. Technetium bone
76–78
Presenting complaints vary,
scans show increased uptake on both sides of the aected disc space (Fig. 25.7A). Bone scans are positive in 74% to 100% of children with discitis
79,80
and can lead to earlier diagnosis and
treatment. MRI also localizes the infection and delineates the extent of so tissue involvement (Fig. 25.7B). In patients who
are refractory to treatment, MRI is useful in assessing whether a so tissue abscess is present.81 MRI shows decreased signal on T1-weighted images and increased signal on T2 images. If an abscess is present, there is peripheral enhancement with the administration of gadolinium.
82
e evaluation of the child with possible discitis also includes obtaining laboratory studies. Elevation of the sedi­mentation rate and C-reactive protein are seen in more than 90% of children with discitis.20 e white blood cell count may be elevated but is less reliable.76 Blood cultures should be obtained and are positive in more than 50% of children with
80
discitis.
In the past, the treatment of discitis was controversial, but now there is agreement that discitis represents a bacterial infection and should be treated with antibiotics.
76,81,83
Cultures of the intervertebral disc are positive in 60% of children, with Staphylococcus aureus the most common organism. A recent study of disc space cultures showed that S. aureus was cultured in 55% and Kingella kingae in 27% of children with discitis.84 Because of the preponderance of S. aureus, and the fact that 40% of cultures from the disc space remain negative, routine aspiration of the aected disc is not recommended.83 If the patient fails to improve quickly with antistaphylococcal anti­biotics, then ne-needle aspiration under CT guidance can be
useful.85 Although administration of a second-generation
Chapter 25 Back Pain in Children and Adolescents 425
SECTION
IV
A
FIG. 25.7 (A) Bone scan in a child with discitis shows increased uptake. (B) Magnetic resonance image reveals
destruction of the disc space, erosion of endplates, and vertebral involvement.
B
cephalosporin for 3 weeks has been recommended,83 epide­miologic trends in antibiotic resistance may alter which anti­biotic should be chosen. Surgical biopsy and debridement are reserved for patients who do not respond to medical manage­ment, have a neurologic decit, have an abscess on MRI, or whose diagnosis is in question.
e outcome of pediatric discitis is favorable. Ten-year radiographic follow-up has shown narrowed disc space (60% of children) or bony ankylosis (40%), but kyphosis is rare and generally mild and patients are pain free.
86
Disc space infection in children younger than 1 year is usually very aggressive and requires immediate diagnosis and treatment. Infants are oen septic at presentation. Residual
kyphosis following eradication of the infection has been described.
87
Vertebral Osteomyelitis
include fever, malaise, weight loss, and night sweats. Neuro­logic ndings occur more frequently in tuberculosis than in
discitis.89 Radiographic changes are more advanced in children with tuberculous spondylitis, and consist of bony destruction of the vertebral body, kyphosis, so tissue abscesses, and so tissue calcications. CT scan ndings include erosions with calcication, and intraspinous, paravertebral, and epidural abscesses.
90,91
A chest radiograph shows evidence of tubercu­losis in 67% of children with tuberculous infection of the spine.90 e puried protein derivative test is usually positive, except in the immunologically challenged child, in whom it remains nonreactive. Pathologic examination of tissue from ne-needle aspiration of the aected bone yields a positive
diagnosis in 83% of children and teens92 and shows epithelioid giant cells and caseous necrosis or tubercle bacilli. Polymerase chain reaction has been used for faster identication of the
organism.
e distinction between discitis and osteomyelitis in children is blurred. It is believed that osteomyelitis is a continuation of discitis,77 with the two entities representing a condition called infectious spondylitis. Osteomyelitis produces more notable vertebral body radiographic changes. Again, S. aureus is the most common organism.
78
Opportunistic infections may also aect the vertebral column, especially in immunocompromised patients such as those with malignancies or who have had organ transplants. Fungal infections such as coccidioidomycosis are rare but must be kept in mind in endemic regions.
88
Tuberculosis is increasing in frequency and is seen most commonly in children from endemic regions. Symptoms
Ankylosing Spondylitis and Rheumatologic Conditions
Ankylosing spondylitis is a rheumatologic condition charac­terized by loss of spinal mobility. It may present in adolescence as back pain. It occurs more frequently in males than in females. Physical ndings include loss of lumbar exibility so that lordosis does not reverse on forward exion, increased kyphosis, and limited chest expansion with inspiration. Plain radiographs may reveal sclerosis, narrowing, or fusion of the SI joints. MRI has been shown to be superior to bone scan in identifying inammation of the SI joint. ation of patients with ankylosing spondylitis shows a high
93,94
Laboratory evalu-
426 PEDIATRICS
A
FIG. 25.8 (A) Anteroposterior radiograph of the thoracic spine of a 16-year-old male with lower extremity
weakness and loss of bladder function shows absence of the spinous process at T2 (arrowheads). (B) Computed tomographic scan delineates the extent of the aneurysmal bone cyst of the posterior elements of T2 (arrowheads).
B
incidence of HLA-B27. Onset of ankylosing spondylitis prior to the age of 16 years has been linked to worse functional outcomes than in adult-onset patients.95 Other rheumatologic conditions linked with back pain include polymyositis, der­matomyositis, and inammatory bowel disease.

Hematologic Conditions

Sickle Cell Anemia
In a recent study of pediatric patients presenting to a Canadian emergency department for the evaluation of back pain, 13% were found to have sickle cell anemia.22 e spine has been reported as the second most common site for pain crisis in these patients, second only to the knee. Anemia is present in 86%.96 Physical examination reveals tenderness to palpation. Treatment is pain management and admission to the hematol­ogy service.
β-alassemia may also produce pain crises that aect the spine. Up to 25% of patients with thalassemia complained of low back pain in a recent study.
97

Neoplasms

Aneurysmal Bone Cysts
Aneurysmal bone cysts (ABCs) are nonmalignant expansile lytic lesions of bone characterized by their vascularity. Although not malignant tumors, they can be locally aggres­sive. eir etiology remains unclear, and a few familial cases have been identied.98 Approximately 15% of ABCs aect the spinal column, with a predilection for the posterior elements. If of sucient size, the lesion may extend into the anterior
column. bone cysts documented that 30% were located in the cervi­cal spine, 30% in the thoracic spine, and 40% in the lumbar spine.
lesion itself, or from an associated pathologic fracture. Neu­rologic compromise is unusual.
99,100
A large multicenter series of spinal aneurysmal
101
Symptoms consist of back pain that can result from the
Radiographs show an expansile lytic lesion with a “bubbly”
appearance. ere is expansion of the cortex. CT scans best
dene the extent of the lesion, and reveal the thin rim of surrounding bone (Fig. 25.8). On occasion, sacral lesions have been shown to aect more than one vertebral level.
102
Treatment of ABCs is surgical curettage with bone gra-
103
ing.
Due to the vascularity of the cysts, preoperative embo­lization is very helpful in reducing intraoperative blood loss and therefore improving visualization.
104–106
Spinal cord moni­toring during embolization has been advocated to avoid vas­cular injury to the spinal cord.
107
Scheduling the surgical resection shortly following embolization is necessary to prevent revascularization of the lesion prior to curettage. When resection of the lesion leads to mechanical instability, simultaneous fusion is recommended.
108
ere is a 10% to 14%
recurrence rate following curettage and graing for spinal
ABCs. A four-step surgical program—consisting of curettage, use of a high-speed burr, electrocautery, and bone graing, with stabilization via short posterior fusion with instrumenta­tion as needed—has been recently proposed, with all patients free from disease at follow-up.
109
Repeat embolizations as well as radionuclide ablation have
been used to denitively treat spinal ABCs in limited cases.
106
Repeat embolization has been advocated in patients who do not have neurologic ndings or pathologic fracture, for whom the diagnosis is certain, or in patients whose lesions have recurred.
110
Osteoid Osteoma
Osteoid osteomas are the most common benign spinal tumor occurring in children, with presentation occurring in the second decade of life. ey typically are located in the poste-
rior elements of the spine. Osteoid osteomas produce back pain that is worse at night, and ameliorated by aspirin or nonsteroidal medication.
Physical examination reveals decreased spinal exibility.
Oen, the patient will stand with a list. e neurologic exami­nation is generally normal.
Chapter 25 Back Pain in Children and Adolescents 427
Plain radiographs are usually insucient to make the diagnosis, but an olisthetic scoliosis might be apparent. When scoliosis is present, the lesion is usually located in the concav­ity of the apex of the curve.
111
Bone scan is positive, with distinct increased uptake seen (Fig. 25.9). CT scans provide the best imaging of osteoid osteomas, with a small radiolucent nidus and surrounding sclerosis and new bone apparent (Fig.
25.10). MRI shows increased signal intensity in the muscles
FIG. 25.9 Bone scan of a 15-year-old male with a 2-year history of back
pain shows increased uptake at T10 (arrow).
and surrounding bone.
112
e MRI appearance, as well as the
tendency for enhancement in the so tissues near the lesion,
may lead the physician to suspect a malignant tumor.
113
Long-term administration of NSAIDs can provide pain relief in a small group of patients with spinal osteoid osteomas; thus, a trial of nonsurgical treatment is warranted. Usually, symptoms are sucient to merit surgical removal of the nidus, which typically results in immediate relief of pain. Intraopera­tive CT imaging has been used to better target the nidus and therefore minimize bony resection.
114
Newer treatments are under investigation, including percutaneous CT-guided burring of the nidus and thermocoagulation.
115,116
When scoliosis has been long-standing, persistence of the deformity is possible following successful removal of the osteoid osteoma.
Osteoblastoma
Although osteoblastoma is a less common benign lesion of the spine, 40% of osteoblastomas are located in the vertebrae.
ey also are located in the posterior elements of the spine, but because they are by denition larger than osteoid osteo-
mas, they oen extend anteriorly into the vertebral bodies.
e primary symptom of osteoblastoma is back pain, which is usually less severe than in osteoid osteoma. Neurologic abnor­malities may result based simply on the size of the lesion and its encroachment on the spinal canal or neural foramina.
e lesion can be usually seen on plain radiographs, but CT scans are invaluable in assessing the size and extent of the osteoblastoma. As in osteoid osteoma, the MRI in osteoblas­toma can overestimate the extent and aggressiveness of the
118
lesion. mately 40% of aected patients.
Plain radiographs also reveal scoliosis in approxi-
111
Treatment is surgical removal of the lesion, with fusion as needed to address instability based on the size of resection. Recurrence occurs in 10% of osteoblastomas.
112
117
SECTION
IV
FIG. 25.10 Computed tomographic scan shows a radiolucent nidus with
surrounding bony sclerosis in an 11-year-old with back pain due to an osteoid osteoma.
Eosinophilic Granuloma/Langerhans Cell Histiocytosis
Eosinophilic granuloma, also known as Langerhans cell his­tiocytosis (LCH) or histiocytosis X, is a peculiar condition of childhood typied by the development of lytic lesions of bone. e lesions may occur singly or aect multiple areas of the skeleton, including the spine. When the condition is associ­ated with systemic involvement, it is known as Hand-Schuller­Christian disease or the more severe Letterer-Siwe disease. LCH has a higher incidence in males. e average age at diagnosis is 6 years, with the majority of patients in their rst
decade of life.
Vertebral lesions in LCH occur in 10% to 17% of aected
children. e patients may present with back pain or a limp. On occasion, neurologic signs can be present.
Radiographs show lytic lesions within the vertebral body or, more rarely, the posterior elements. Larger lesions lead to collapse of the vertebral body, which can be either symmetric or asymmetric (Fig. 25.11). Although vertebra plana (also known as coin-on-end appearance) is the classically described spinal lesion in LCH, it has been reported that only 40% of
119
428 PEDIATRICS
children with LCH and vertebral lesions have vertebra plana.
120
Skeletal surveys oen result in the identication of other sites
of involvement, which supports the diagnosis. Typical sites of involvement include the skull, the pelvis, and the diaphysis of the long bones. Bone scan is positive in 90% of children with LCH.
121
e dierential diagnosis includes leukemia, infection,
and other malignant tumors, such as Ewing sarcoma.
122
If the radiographic appearance is atypical and other peripheral skeletal lesions are not identied, a surgical biopsy of the
spinal lesion is warranted. Pathologic specimens show clonal proliferation of Langerhans-type histiocytes, eosinophils, and giant cells.
123
Most patients with LCH experience spontaneous resolu­tion of their disease. Because the condition appears to be self-limiting, the indications for treatment are few. Back pain due to a unifocal spinal lesion can usually be relieved by rest and the use of orthoses.
119,123
Patients with neurologic compromise may be treated with low-dose radiation therapy or surgical debridement of the lesion and stabilization.
121,124
Radiation therapy has fallen out of favor as treatment for LCH of the spine due to the potential for secondary malignancies. Multifocal disease, particularly when associated with systemic involvement, is treated with chemotherapy.
125
e long-term outcome of LCH in the absence of systemic
disease is very good. Recurrence of disease is not seen in chil-
125,126
dren. seen, although complete restoration to normal is unusual.
Over time, improvement in vertebral body height is
127,128

Malignant Tumors

Leukemia
Leukemia is the most common pediatric malignancy that pro­duces back pain. Many children rst present to the orthopaedic
surgeon; reports indicate that 6% to 25% of children with acute leukemia present initially with back pain. children are initially misdiagnosed; thus, the orthopaedic surgeon must have a high level of suspicion to properly evaluate this population.
131
e history may reveal symptoms of pallor, fatigue, loss of appetite, or fever. e parent should be ques­tioned about a history of bruising or abnormal bleeding.
Radiographic ndings are not always initially present but
include generalized osteopenia, vertebral compression frac­tures, and metaphyseal leukemic lines. Of children with acute lymphoblastic leukemia, 7% have vertebral compression fractures
130,132
(Fig. 25.12).
e diagnosis can usually be made on laboratory examina­tion, with abnormalities seen in any or all of the three cell lines, that is, anemia, thrombocytopenia, and leukopenia. e sedimentation rate is usually elevated. Of children with leuke­mia, 10% or more will initially have normal automated
132,133
counts.
Inspection of the peripheral smear will reveal the
diagnosis in some of these children.
Chemotherapy under the direction of pediatric oncology is the treatment of choice. Spinal bracing can be prescribed to relieve back pain and prevent further compression fractures.
129,130
Many of these
FIG. 25.11 Lateral radiograph of a 12-year-old male with vertebra plana of
T11 consistent with eosinophilic granuloma (arrowheads). Back pain resolved with conservative treatment.
FIG. 25.12 Osteopenia and multiple compression fractures in a child
presenting with back pain due to leukemia.
Chapter 25 Back Pain in Children and Adolescents 429
Vertebral Malignant Tumors
Malignant tumors of the spine cause signicant back pain in over 50% of children at the time of diagnosis. they must remain in the dierential diagnosis of pediatric
back pain. Pain may radiate into the legs, resembling the symptoms of a herniated disc. While patients with disc hernia­tion are in their second decade of life, children with spinal or spinal cord tumors may be younger. Neurologic decits and
reex changes are uncommon in disc herniation but frequent in tumors.
135
Vertebral tumors include Ewing sarcoma and osteosar-
136
coma.
Osteosarcoma rarely aects the spine.
are variable, with osteolytic, osteoblastic, and mixed appear­ances possible. CT and MRI are used to stage the tumor. Treatment is dicult.
Up to 10% of Ewing sarcomas occur in the spine, with the
sacrum the most frequent site.
tion is 13.3 years.
139
Symptoms consist of relentless back pain.
138
e average age at presenta-
Neurologic decits are present in 58% of patients with spinal
Ewing tumors.
140
Radiographs may show an expansile lytic lesion with variable vertebral collapse. Cases of Ewing sarcoma that radiographically resemble vertebra plana have been reported, leading to the misdiagnosis of eosinophilic granu-
140
loma.
MRI delineates the extent of the lesion and its accom-
panying so tissue mass.
134
Although rare,
137
Radiographs
Spinal Metastasis

Nonorthopaedic Causes of Pain

Intraabdominal processes such as inammatory bowel disease, hydronephrosis, ovarian cysts, endometriosis, and urinary tract infections can produce back pain. Pain due to these conditions is not exacerbated by activity and tends to be more intense at night. Pediatric referral should be made when nonmusculoskeletal causes are suspected.

Psychosomatic Pain (Conversion Reaction)

As discussed in the beginning of this chapter, there are children in whom an organic etiology for back pain cannot be found despite thorough evaluation. Back pain can be inuenced by psychosocial factors that alter the patient’s perception of pain and the eect of pain on everyday life. Psychosomatic pain remains a diagnosis of exclusion. It is more prevalent in ado­lescence, particularly in those teens whose family members have a history of similar back pain. A detailed social history oen reveals problems at home or school, oen resulting in
anxiety and depression. Treatment is dicult but includes intervention by a psychologist and physical therapy. Recent studies show that up to 71% of children and adolescents who have negative diagnostic evaluations for back pain continue to have pain at an average of 4.4 years of follow-up.19 Even 8 years aer initial evaluation, 62% of 58 patients were still symptomatic.
146
SECTION
IV
Neuroblastoma is the most frequent tumor to metastasize to the spine in children. tumors, neuroblastoma represented one-third of all cases.
141
In a recent study of 29 malignant spine
134
Radiographs usually show diuse vertebral involvement. e
thoracic spine is most frequently involved. An elevation of urinary normetanephrine may help diagnosis.
138
Other tumors that involve the spine include rhabdomyosarcoma, Wilms tumor, and primary neuroectodermal tumors.
142
Spinal Cord Tumors
Common spinal cord tumors in children are astrocytomas and ependymomas. e onset of symptoms is indolent. Neurologic signs such as deterioration of gait, delay in motor skills, and loss of bladder control raise suspicion. usually present, leading to initial referral to the orthopaedic surgeon in 31% to 58% of patients who are eventually diag­nosed with spinal cord tumors.
143,144
reveals motor decits, clonus, and possibly scoliosis. ere may be limitation of spinal exibility. Radiographs can show changes due to pressure or expansion of the tumor, including absence or thinning of the pedicle or widening of the inter­vertebral foramina. Spinal cord tumors are best seen on MRI.
Although uncommon, neurobromas in children and
adolescents with neurobromatosis can undergo malignant degeneration into neurobrosarcoma. Back pain in a patient with neurobromatosis should be evaluated.
143–145
Back pain is
Physical examination

KEY POINTS

Use of Diagnostic Tests
Radiograph: History of signicant trauma; night pain, fever or
inability to walk; age 8 years or younger; duration of pain greater than 2 months
Bone scan: Negative plain radiograph with normal neurologic
examination, persistent pain, history of athletic overuse
CT scan: Positive plain radiograph or bone scan MRI: Abnormal neurologic examination, painful scoliosis in
patient younger than 8 years, painful le thoracic scoliosis
Laboratory tests: Night pain, fever, age younger than 8 years,
constant pain
Likely Diagnoses Based on Age
Younger than 5 years: Tumor, discitis Age 5 to 10 years: LCH, discitis, tumor/leukemia Age 10 to 18 years: Musculoskeletal back pain, lumbar
Scheuermann disease, herniated disc or apophysis, spon­dylolysis, osteoid osteoma, tumor/leukemia

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430 PEDIATRICS
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3. Yang S, Werner BC, Singla A, Abel MF. Low back pain in adolescents: a 1-year analysis of eventual diagnoses. J Pediatr Orthop. 2015. Epub ahead of print.
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5. Balagué F, Skovron ML, Nordin M, et al. Low back pain in schoolchildren. A study of familial and psychological factors. Spine. 1995;20(11):1265-1270.
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SECTION
IV
432 PEDIATRICS
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