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Clinical, laboratory, and radiographic features of selected causes of hip pain in children unrelated to acute trauma or fracture

Clinical, laboratory, and radiographic features of selected causes of hip pain in children unrelated to acute trauma or fracture
Cause Typical age/risk factors Clinical features Laboratory features Radiographic features
Infectious
Septic arthritis of the hip

0 to 6 years

M>F

Fever and ill-appearance

Pain with any active or passive motion and refusal to bear weight

Preferred position: Flexion, abduction, and external rotation of the hip

Elevated WBC count (>12,000 cells/microL), ESR (>40 mm/hour), and CRP (>2 mg/dL [20 mg/L])

Positive synovial fluid or blood culture
Unilateral joint effusion
Septic arthritis of the sacroiliac joint Late childhood

Pain over sacrum

Fever

Pain with maneuvers that twist the pelvis (eg, positive FABERE test)

Elevated WBC count, ESR, CRP

Positive synovial fluid or blood culture

Widening of the joint space

Blurring of the subchondral plate
Lyme disease

Any age

Residence in or travel to Lyme endemic region

Fever uncommon

Willing to bear weight
IgG antibodies to Borrelia burgdorferi  
Osteomyelitis of femoral head or pelvis  

Fever and ill appearance

Localized pain

Decreased mobility (but may permit passive motion of the hip)
Elevated WBC count, ESR, and CRP

Early (3 to 7 days): deep soft-tissue swelling; obliteration of fat pads

Late (10 to 21 days): lytic sclerosis; periosteal new bone formation
Psoas abscess (referred pain)   Pain is increased with hip extension but diminished with hip flexion Elevated WBC count, ESR, and CRP

Loss of psoas muscle definition

Abnormal soft tissue shadows

(CT is preferred study)
Appendicitis or abdominal/pelvic abscess (referred pain) Any age Associated gastrointestinal complaints (pain, vomiting, anorexia) Elevated WBC count, ESR, CRP

Calcified appendicolith

(US is usually the preferred initial imaging study)
Discitis (referred pain) 0 to 5 years

Loss of lumbar lordosis

Refusal to bend forward

Minimal systemic toxicity

WBC count usually normal

Elevated ESR

Narrowing of intervertebral joint space after two to three weeks of symptoms, followed by destruction of vertebral end-plated and disc herniation

Diagnosis is best made by MRI
Inflammatory
Transient synovitis

3 to 8 years

M>F

Fall/winter season

Afebrile

Well-appearing

WBC count <12,000 cells/microL

ESR <20 mm/hour

CRP <2 mg/dL (20 mg/L)
Unilateral or bilateral joint effusion
Systemic arthritis
  • Juvenile idiopathic arthritis (formerly juvenile rheumatoid arthritis)
  Rarely causes isolated hip pain

Elevated ESR and/or CRP

Positive ANA, RF, or CCP in some cases

Joint space narrowing

Erosive changes of the femoral head and acetabula
  • Infectious arthritis (eg, Lyme arthritis, acute rheumatic fever, disseminated gonorrhea)
Variable ages Associated clinical features of underlying infection Depend upon underlying infection  
  • Postinfectious or reactive
Variable ages History of antecedent respiratory, gastrointestinal, or genitourinary infection

Elevated ESR or CRP

Evidence of antecedent or concomitant infection
Evidence of enthesitis or arthritis
Idiopathic chondrolysis of the hip 10 to 20 years

Insidious onset

Decreased range of motion in all planes

Absence of systemic symptoms
None Narrowing of the joint space, osteopenia, protrusion acetabuli, and premature physial fusion
Chronic recurrent multifocal osteomyelitis

Any age

F>M

Fever (rarely)

Bone pain

May be associated with pustular eruption on palms and soles
Elevated ESR or CRP (sometimes)  
Mechanical/orthopedic
Slipped capital femoral epiphysis

Early adolescence

Mean age:
Females: 12 years
Males: 13.5 years

M>F (slightly)

Obesity

Endocrine disorders

Bilateral in 20 to 40% of cases

Pain may be localized to the knee or thigh
Normal WBC count, ESR, CRP

Nondisplaced: Normal or widening and irregularity of the capital femoral physis, osteopenia, and increased density of the metaphysis

Displaced: Posterior displacement of femoral epiphysis
Avascular necrosis
  • Legg-Calvé-Perthes disease

3 to 12 years

M>>F

Insidious onset

Pain increases with activity
Normal WBC count, ESR, CRP

Early: Joint space widening and subchondral fracture

Late: Sclerosis, fragmentation, subchondral collapse of the ossification center
  • Secondary avascular necrosis
Variable ages Signs and symptoms of underlying condition (eg, renal failure, glucocorticoid use, systemic lupus erythematosus) Depend upon underlying condition

Early: Joint space widening and subchondral fracture

Late: Sclerosis, fragmentation, subchondral collapse of the ossification center
Femoral stress fracture

Adolescents and young adults

Endurance sports

Pain may localize to the anterior thigh

Pain reproduced with hopping on affected leg
Normal WBC count, ESR, CRP Periosteal elevation, cortical thickening, sclerosis, fracture line
Muscular strain Any age

Pain with movement

Weakness
Normal WBC count, ESR, CRP  
Iliac apophysitis

Adolescents

Sports that involve twisting (eg, golf), sprinting, and kicking

Pain and swelling at iliac crest

Slowly progressive pain with activity
Normal WBC count, ESR, CRP  
Snapping iliopsoas tendon Young athletes (ballet, karate)

Snapping sensation in anterior groin

Sensation may be reproduced by bringing the hip from a flexed abducted position to an extended adducted position
Normal WBC count, ESR, CRP Catching of the posterior iliotibial band or anterior portion of the gluteus maximus muscle over the greater trochanter can be seen on dynamic ultrasonography
Trochanteric bursitis  

Lateral hip pain over the outer thigh

Pain aggravated by direct pressure
Normal WBC count, ESR, CRP Calcification occasionally present in the region of the bursa or adjacent soft tissues
Acetabular labral tear

Adolescent athletes, particularly sports that involve pivoting or twisting

History of Legg-Calvé-Perthes disease or SCFE

Snapping, catching

Pain with internal rotation and extension
Normal WBC count, ESR, CRP  
Femoroacetabular impingement Dancers

Groin pain with turning, twisting, and squatting

Pain is reproduced with flexion and internal rotation of the hip
Normal WBC count, ESR, CRP Nonspherical femoral head; lack of femoral head-neck offset; acetabular overcoverage
Neoplastic
Osteoid osteoma 10 to 20 years

Nocturnal pain

Prompt relief with NSAIDs
  Osteoid nidus with or without calcification (osteoid nidus may be obscured by dense sclerosis)
Malignant neoplasms, primary or metastatic (eg, leukemia, lymphoma, Ewing sarcoma, etc) Variable ages

Nighttime pain

Constant pain (unchanged by activity)

Pain <3 months duration

Systemic symptoms (eg, fever, weight loss)

Abnormal CBC (anemia, leukopenia, thrombocytopenia)

Elevated LDH, uric acid

Bony destruction

Subtle signs of space-occupying lesion (separation or thinning of the pedicles)
Pigmented villonodular synovitis Adults

Recurrent joint effusions

Minimal pain
  Well circumscribed areas of bone erosion
M: male; F: female; WBC: white blood cell; ESR: erythrocyte sedimentation rate; CRP: C-reactive protein; FABERE: Flexion of the hip and knee, ABduction and External Rotation of the hip, Extension of the opposite hip (also called the figure-of-four test); IgG: immunoglobin G; CT: computed tomography; US: ultrasonography; MRI: magnetic resonance imaging; ANA: antinuclear antibodies; RF: rheumatoid factor; CCP: cyclic citrullinated peptides; SCFE: slipped capital femoral epiphysis; NSAIDs: nonsteroidal anti-inflammatory drugs; CBC: complete blood count; LDH: lactate dehydrogenase.
Graphic 89604 Version 5.0

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