9
Imaging of children’s hips 1 D WILSON, MBBS, BSc, FRCP, FRCR and 2 G ALLEN, BM DCH, MRCGP, MRCP, FRCR 1 Nuffield Orthopaedic Centre, Oxford and 2 Royal Orthopaedic Hospital, Birmingham, UK Children may present with hip disease in a variety of ways. In the newborn it may be detected by routine clinical examination. In the older child pain, stiffness and limping are the primary symptoms. In the toddler ‘‘going of their feet’’ may be the presenting event. Most children who complain of pain in the hip have genuine pathology. It is an unusual location for a child to make up or exaggerate complaints. Imaging has a pivotal role in the management of these patients who may have disease that requires urgent medical or surgical treatment. In most cases a child or infant complaining of a painful hip should be examined and investigated as a matter or urgency. Hospitals should provide on-call imaging and general practitioners should be fully aware of local facilities and management protocols. Developmental dysplasia Between 1 and 3 newborns per 1000 live births will be diagnosed as suffering from developmental dysplasia of the hip (DDH), formerly known as congenital dislocation of the hip, with a female preponderance of 9:1. This hides the much larger incidence of premature osteoarthritis that devel- ops in young adults who have a shallow and mechanically disadvantaged hip that is not bad enough to have presented in infancy. Many who undergo hip replacement in their middle years are undiagnosed cases of DDH. The true incidence of DDH is therefore much higher, although there are no clear figures in the literature (Figures 1 and 2). There is good evidence that early treatment of DDH with splint therapy improves prognosis [1]. This is only effective in the first 6 months of life when remodelling is very active. Therefore if diagnosis is made early enough, overall popula- tion morbidity may be reduced. It was this rationale that led to the now universal clinical screening protocols using Barlow and Ortolani manoeuvres to detect subtle subluxation and instability of the hip. Unfortunately clinical examination, even in the best of hands, will overlook a substantial proportion of cases that would benefit from early treatment. Ultrasound introduces an additional method of screening that considerably improves detection [2–7]. A number of methods have been developed and each has strong and sometimes vehement advocates. In reality, local outcome measures must be the standard by which these techniques are judged. The best method applied badly or administered ineffectively will be of less use than a less technically demanding method that is used rigorously with top quality clerical and management support. Figure 1. Plain radiograph of a 28-year-old who has early osteoarthritis secondary to developmental dys- plasia that was asymptomatic as a child and young adult. Summary N Ultrasound is an important tool in the detection and management of developmental dysplasia of the hip. N Universal screening for developmental dysplasia of the hip by ultrasound may be wise but there is currently insufficient evidence to clearly recommend this a national policy. N A painful hip in childhood is a clinical emergency. N Ultrasound is the definitive method for detecting joint effusion. N Ultrasound cannot determine whether a joint effusion is due to infection, haemorrhage or transudate. N Imaging has a role in determining the cause of snapping hips. Imaging, 14 (2002), 179–187 E 2002 The British Institute of Radiology 179 Imaging, Volume 14 (2002) Number 3

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Imaging of children’s hips

1D WILSON, MBBS, BSc, FRCP, FRCR and 2G ALLEN, BM DCH, MRCGP, MRCP, FRCR

1Nuffield Orthopaedic Centre, Oxford and 2Royal Orthopaedic Hospital, Birmingham, UK

Children may present with hip disease in avariety of ways. In the newborn it may be detectedby routine clinical examination. In the older childpain, stiffness and limping are the primarysymptoms. In the toddler ‘‘going of their feet’’may be the presenting event.

Most children who complain of pain in the hiphave genuine pathology. It is an unusual locationfor a child to make up or exaggerate complaints.Imaging has a pivotal role in the management ofthese patients who may have disease that requiresurgent medical or surgical treatment.

In most cases a child or infant complaining of apainful hip should be examined and investigatedas a matter or urgency. Hospitals should provideon-call imaging and general practitioners shouldbe fully aware of local facilities and managementprotocols.

Developmental dysplasia

Between 1 and 3 newborns per 1000 live birthswill be diagnosed as suffering from developmentaldysplasia of the hip (DDH), formerly known ascongenital dislocation of the hip, with a femalepreponderance of 9:1. This hides the much largerincidence of premature osteoarthritis that devel-ops in young adults who have a shallow andmechanically disadvantaged hip that is not badenough to have presented in infancy. Many whoundergo hip replacement in their middle years areundiagnosed cases of DDH. The true incidence ofDDH is therefore much higher, although there areno clear figures in the literature (Figures 1 and 2).

There is good evidence that early treatment ofDDH with splint therapy improves prognosis [1].This is only effective in the first 6 months oflife when remodelling is very active. Therefore ifdiagnosis is made early enough, overall popula-tion morbidity may be reduced. It was this rationalethat led to the now universal clinical screeningprotocols using Barlow and Ortolani manoeuvresto detect subtle subluxation and instability of thehip. Unfortunately clinical examination, even inthe best of hands, will overlook a substantialproportion of cases that would benefit from earlytreatment. Ultrasound introduces an additionalmethod of screening that considerably improvesdetection [2–7]. A number of methods have beendeveloped and each has strong and sometimes

vehement advocates. In reality, local outcome

measures must be the standard by which these

techniques are judged. The best method applied

badly or administered ineffectively will be of less

use than a less technically demanding method that

is used rigorously with top quality clerical and

management support.

Figure 1. Plain radiograph of a 28-year-old who hasearly osteoarthritis secondary to developmental dys-plasia that was asymptomatic as a child and youngadult.

Summary

N Ultrasound is an important tool in the detection

and management of developmental dysplasia

of the hip.

N Universal screening for developmental

dysplasia of the hip by ultrasound may be wise

but there is currently insufficient evidence to

clearly recommend this a national policy.

N A painful hip in childhood is a clinical

emergency.

N Ultrasound is the definitive method for

detecting joint effusion.

N Ultrasound cannot determine whether a joint

effusion is due to infection, haemorrhage or

transudate.

N Imaging has a role in determining the cause of

snapping hips.

Imaging, 14 (2002), 179–187 E 2002 The British Institute of Radiology

179Imaging, Volume 14 (2002) Number 3

Page 2: Children's hip

Most techniques stem from that developed by

Professor Graf, an Austrian orthopaedic surgeon.

Graf uses coronal plane ultrasound to produce a

standard section equivalent in orientation to a

frontal radiograph of the hip. Lines drawn on the

image are used to measure the angular depth of

the acetabulum and the cover of the femoral head.

Strict adherence to the technique is essential as

small variations in measurement will alter classi-

fication and affect management protocols. Others

have introduced less demanding methods of mea-

surement, although still requiring discipline in

image acquisition (Figures 3–5). It has been

argued that a static image alone is less sensitive

than a morphological measure plus a dynamic

stress test, and there is evidence that this improves

detection [8]. In most practices a combination of

static and dynamic imaging is employed [9, 10].

More contentious is deciding upon the popula-

tion to be screened. Infants with family history of

hip dysplasia, those born by breech delivery and

those with other congenital anomalies are at much

higher risk of developing DDH. Screening of

those at high risk in addition to those who are

suspected as being abnormal on routine clinical

examination is the most common practice in the

UK. Others argue that this policy will fail to

provide the most accurate and sensitive detection

of all who might benefit from early treatment and

suggest universal screening [11]. In Austria and

Germany, child benefit entitlement is linked to

attending for screening. One counter to this

Figure 3. Ultrasound of a borderline depth acetabu-lum with measurement using the Morin method.

Figure 4. Ultrasound of a shallow acetabulum thatwould be treated by a splint or harness.

Figure 5. Ultrasound of a dislocated hip that requiredsurgical reduction.

Figure 2. Plain radiograph of a pseudarthrosis result-ing from unrecognized dislocation of the hip.

D Wilson and G Allen

180 Imaging, Volume 14 (2002) Number 3

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argument is that required resources are not costeffective, although this is a difficult line to take inwhat is an emotionally charged topic. Indeedthere is evidence that the overall saving inresources is conquerable in all screening strategies[12, 13]. More telling is the point that standards ofdetection are likely to drop in any universalscreening project and that there is currently noevidence that overall population outcome is betterin those centres where it is practiced. Furtherepidemiological research is required before firmrecommendations can be made, and currentadvice in the UK is to perform ultrasoundscreening in infants in the high risk category only.

In complex congenital hip disorders a combina-tion of ultrasound, plain radiography and MRIare indicated, especially for planning surgery [14,15]. For example, in deficiency of the proximalfemur either ultrasound or MRI may be used todetect whether there is a cartilage fragment in thegap and to determine the integrity of the hip joint[16].

Following surgery or splint therapy, MRI isuseful to assess the degree and efficacy of reduc-tion [17]. In managing pelvic and femoralosteotomies the information from cross-sectionalimaging is important [18, 19].

Irritable hip

Children between the ages of 3 years and 12years commonly suffer from acute episodes of hippain. The vast majority are suffering fromtransient synovitis, which is a benign and self-limiting condition. Unfortunately, a small butimportant minority have a more serious com-plaint such as septic arthritis and need urgentsurgical management to minimize long-termdisability [20]. The challenges are detecting andtreating this small subset whilst treating the painand discomfort of the majority in a timely andsafe manner.

Transient synovitis

The cause of transient synovitis is not known.There are postulates that it is traumatic orinfective in origin, but neither is proven. Thecondition presents with a short history of painand limping, which typically resolves within 3–4days. Although MRI, CT and ultrasound will alldetect effusions [21], ultrasound is the establishedmethod of choice as it is readily available, easy toperform and extremely accurate [22–24]. Ultrasoundexamination shows a joint effusion with capsulardistension and a varied amount of synovial thicken-ing. A difference of 2 mm or more between thehips is significant. Joint aspirate will be clear andstraw coloured and depressurizing the joint leads

to immediate pain relief [25, 26]. There are noorganisms present on Gram stain and culture willbe negative.

Pain may be treated with analgesia, however,this is not very effective. Some advocate skintraction and bed rest but this requires hospitaladmission. A diagnostic aspirate of the joint is amore effective method of analgesia as there isinstant pain relief and restoration of function.Local anaesthetic jelly and ultrasound guidanceallow a safe and rapid joint puncture and preventhospital admission in many cases.

Septic arthritis

Pyogenic organisms may infect the hip via ablood borne route. Staphylococcus aureus andhaemophylus influenzae are the most commonorganisms. If infection is untreated the joint willbe rapidly destroyed. Consequent septicaemiamay be life threatening. The only effective therapyis a combination of arthotomy with joint lavageand intravenous antibiotics. Clinical presentationis often indistinguishable from transient synovitis.Fever and serological signs of inflammation areoften absent. The degree of irritability does notpredict diagnosis and ultrasound appearances ofseptic arthritis are no different from transientsynovitis [27]. The only effective means of diag-nosis is aspiration, Gram stain and culture.Fortunately the condition is rare and those whorely on ineffective methods of diagnosis will onlyrarely cause permanent damage.

Perthes disease

Osteochondrosis of the hip, Legg–Calve–Perthes disease, is an uncommon disease ofunknown cause. The most convincing theory isthat it is the result of trauma in an immaturejoint. Again, presentation is with pain andlimitation of movement. The child may be older(7–14 years) and there is sometimes a history ofprevious episodes of pain. Plain radiography isdiagnostic showing fragmentation, roughening,flattening and distortion of the femoral capitalepiphysis (Figures 6–8). In the early phase theplain radiograph shows widening of the hip jointowing to cartilage overgrowth. Long-term dis-ability may result owing to alteration in shape andmechanical stress. Treatment is based aroundsurgery designed to confine the femoral headwithin the joint, and often includes pelvic andfemoral osteotomies. Ultrasound examination inthe early stages of the condition will show jointeffusion [5, 28–30] and the fragmented epiphysismay be visible, but this method should not berelied upon. For older children with an irritablehip a plain radiograph is mandatory to exclude

Imaging of children’s hips

181Imaging, Volume 14 (2002) Number 3

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slipped epiphysis and Perthes disease [31]. Children

with recurrent irritable hip should be examined by

MRI as this technique may detect the condition

when plain radiograph changes have not yet

occurred [32–37] (Figure 3). Gadolinium (Gd)

DTPA enhancement may prove to be useful in

predicting osteonecrosis by assessing vascularsupply to the epiphysis [38]. MRI also hasimportant roles in surgical planning and indetecting occult disease in the opposite hip. It isalso valuable in assessing the late sequelae ofPerthes disease [39, 40].

Slipped epiphysis

Older children (8–14 years) may suffer fromslipped upper femoral capital epiphysis (SUFE).This typically occurs in boys heavier than averageand is thought to be the result of mechanicalstress on the immature growth plate. Presentationis also with pain and limping of short duration.The only effective treatment is surgical fixation,most commonly achieved by inserting pins intothe epiphyses via the femoral neck. If treatment isdelayed the slip will worsen with considerablyincreased risk of osteonecrosis in the displacedepiphysis and severe long-term consequences [41,42]. Detection and treatment are therefore urgent.Whilst ultrasound will show an effusion in 75% ofcases, and may show the step in the contour of thefemoral head [43–45], it is not as safe andeffective as plain radiograph examination using afrog lateral projection. SUFE represents a Salter–Harris 1 type lesion of the proximal femoralepiphysis. The slip most often occurs in a postero-medial direction and may be difficult to see onanteroposterior (AP) radiography [46]. A froglateral is mandatory. It is reasonable to omit theconventional AP film to reduce radiation dose tothe patient. MRI is useful to asses direction andseverity of the slip, especially in planning surgery[47]. It is particularly useful in detecting occult orsubtle slip in the opposite asymptomatic hip,which may occur in up to 60% of cases. Thisexamination should be performed prior to surgeryon the affected hip as prophylactic pinning underthe same anaesthetic is possible [48] (Figures 9–11).

Investigation of irritable hip

From the above it should be apparent that achild with an irritable hip should be seen as anemergency. The clinician should take a historyand confirm the hip as the origin of pain byclinical examination. Ultrasound examinationshould be arranged as an emergency [49, 50]. Ifthere is no joint effusion plain radiography shouldbe undertaken [44, 45]. If this is normal then othercauses of pain should be considered, e.g. retro-caecal appendicitis, muscle strain and referredback pain.

If ultrasound examination shows fluid, atherapeutic and diagnostic aspiration should beperformed. Fluid should be sent for urgent Gramstain and culture (Figures 12 and 13).

Figure 7. The same child as in Figure 6, 1 monthlater, showing contour changes and sclerosis ofPerthes disease.

Figure 8. Established Perthes disease with frag-mentation and flattening of the right femoral capitalepiphysis.

Figure 6. A frog lateral view of a child with sus-pected slipped upper femoral capital epiphysis;appearances are normal.

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182 Imaging, Volume 14 (2002) Number 3

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In older children (over 8 years) plain radiog-raphy in a frog lateral should be performed.

In complex or recurrent cases, MRI should beconsidered as an additional investigation [51, 52].If MRI is not available there is a role for isotopebone scintigraphy to detect occult bone lesions[53].

Osteomyelitis

Bone infection may be primary due to bloodborne organisms or secondary due to implantation,surgery or other forms of trauma. Occasionallyinfection spreads to bone from septic arthritis.

Presentation varies greatly from an acutely

painful region, immobility and systemic toxicity

through to a completely occult disease with minimal

local symptoms and just s general sense of ill

health.Acute infection is typified by bone oedema and

subperiosteal reaction. The latter may be seen on

plain radiography but both are readily apparent

on MRI. The oedema extends beyond the area

that is histologically identifiable as active inflam-

matory response but it is difficult, if not impossible,

to distinguish this margin using imaging. It has

been suggested that areas of true infection would

enhance with intravenous Gd DTPA injection on

Figure 10. 6 weeks after the image in Figure 9, theslip was recognized. There is now significant change,the epiphysis being rendered avascular with a pooroutcome.

Figure 11. MRI of advanced slipped epiphysis.

Figure 12. Ultrasound of a normal hip without aneffusion.

Figure 9. Early slipped epiphysis missed as the subtlechanges were not noticed and a lateral view was notperformed.

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183Imaging, Volume 14 (2002) Number 3

Page 6: Children's hip

MRI, however, this is not a reliable test and in

practice it is rare for contrast enhancement to

assist in management. Subperiosteal reaction may

be detected using ultrasound. A positive finding

on ultrasound is very specific but a negative study

does not exclude acute osteomyelitis.Chronic infection and acute infection after

antibiotic therapy are best studied by a combina-

tion of plain radiographs to detect bony destruc-

tion and sclerosis, with MRI to show the extent of

diseased bone, abscess within and outside bone

and the extent and nature of soft tissue involve-

ment [54]. Ultrasound is useful in excluding or

defining soft tissue abscesses [55]. CT is sometimes

useful in defining the shape and extent of sclerotic

sequestered fragments. The response to drug

treatment and planning of surgical debridement

depends very much on follow up studies. Serial

MRI studies are invaluable in deciding timing and

extent of surgery. Again, contrast enhancement

rarely alters clinical decisions.Tumours may mimic infection and vice versa.

In most cases biopsy is indicated and MRI will be

important in deciding where to biopsy and via

which route. Infection in bone is notorious for the

difficulty in identifying the organisms. Even in

proven and definite osteomyelitis only 30% of

biopsy specimens will grow organisms. For this

reason it is important to send biopsy material for

histological examination as this is more often the

means by which infection is established. Image

guided needle biopsy is valuable. However, in

children an open biopsy under general anaesthesia

is not only kinder but may also treat symptoms

as the marrow oedema may be depressurized,

relieving some of the pain.

Juvenile arthritis

Juvenile arthropathy may present in the hip,although other joints such as the wrist or kneesare more common presenting locations. It shouldbe considered as a possible diagnosis in recurrentor complicated cases where diagnosis of transientsynovitis is in doubt. Synovial reaction will bevisible on ultrasound as thickening and irregular-ity of the capsule. MRI may be more difficult tointerpret as the high signal from fluid in the jointseen on T2 weighted or short tau inversion recovery(STIR) images will be the same signal as exhibitedby thickened and oedematous synovium [56](Figure 14). Intravenous Gd DTPA enhancementwould resolve this issue but ultrasound is cheaper,faster and more acceptable to the patient. Ultrasoundis the imaging method of choice for detectingeffusion and pannus [57] and it has a very usefulrole in follow-up studies [58].

Trauma

Fractures and dislocations around the hipare rare in children [59, 60]. They tend to beassociated with high energy injuries. Fracturesshould be apparent on plain radiography butminimally displaced fractures and stress lesionsmay not. MRI is the definitive test and will showall fractures as low signal lines on T1 weightedimages surrounded by high signal material on T2

weighted or STIR sequences. MRI also has a rolein complex fractures of the acetabulum when CT isnot conclusive [61]. Non-accidental injury should

Figure 14. T2 weighted coronal MRI of a joint effu-sion and synovitis in juvenile arthritis.

Figure 13. Ultrasound of a hip with a substantialeffusion. Aspirate was sterile. The appearances ofseptic arthritis may be identical.

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184 Imaging, Volume 14 (2002) Number 3

Page 7: Children's hip

always be considered in younger age groups.Ultrasound can also pick up fractures in theyounger patient.

Acute chondral injuries due to sheering forcesmay cause an acute arthropathy. If there is aresulting defect in the articular surface, symptomsmay persist and fail to resolve. Conventional MRImay show the lesion especially on T2 weighted fastspin echo images, although it may be necessary toperform MR arthrography to be sure. CT arthrog-raphy is also effective but is less suitable inchildren as the radiation burden is large.

Muscle strains and tears may mimic irritablehip. They may be invisible on all imaging butsignificant tears will be well seen on ultrasound asdefect in the myofibrillar structure, oedema andscar tissue. Dynamic stress ultrasound will showmuscle tears by the retraction of muscle andbulging of the margins of the tear. In the acutephase, MRI of the affected area may be the mostsensitive test.

Growth plate injuries are a particular problemin children. Their management depends on theextent and the skeletal age of the child. MRI isthe best method of studying the nature of theinjury [62].

Snapping hip

A variety of clicks and snaps may occur aroundthe hip. These are most common in teenage girls.They include iliopsoas snaps, iliotibial tractsnapping, greater trochanteric bursitis and glenoidlabral injuries. Static ultrasound will demonstrateinflamed bursae and thickening whilst dynamicultrasound is much more useful as it will show theclicking or snapping tendon [63–65]. Local anaes-thetic blocks of the snapping tendon guided byimaging are useful in confirming diagnosis whenmore invasive forms of treatment are beingconsidered. Labral tears will only be visible onMRI or CT arthrography [66–69]. They are morecommon anteriorly than superiorly and imagingshould include axial sections following the jointinjection.

References

1. Teo EL. Clinics in diagnostic imaging (69). Bilateraldevelopmental dysplasia of the hip. Singapore MedJ 2002;43:49–52.

2. Berman L, Klenerman L. Ultrasound screening forhip abnormalities. Preliminary findings in 1001neonates. BMJ 1986;293:719–22.

3. Novick G. Sonography in paediatric hip disorders.Radiol Clin North Am 1988;26:29–53.

4. Castelein R, Sauter A, et al. Natural history ofultrasound hip abnormalities in clinically normalnewborns. J Pediatr Orthop 1992;12:423–7.

5. Terjesen T. Ultrasonography in the primary evalua-tion of patients with Perthes disease. J PediatrOrthop 1993;13:437–43.

6. Terjesen T. Ultrasound as the primary imagingmethod in the diagnosis of hip dysplasia in childrenaged ,2 years. J Pediatr Orthop B 1996;5:123–8.

7. Poul J, Bajerova J, et al. Selective treatmentprogram for developmental dysplasia of the hip inan epidemiologic prospective study. J PediatrOrthop B 1998;7:135–7.

8. Finnbogason T, Jorulf H. Dynamic ultrasono-graphy of the infant hip with suspected instability.A new technique. Acta Radiol 1987;38:206–9.

9. Joseph KN, Meyer S. Discrepancies in ultrasono-graphy of the infant hip. J Pediatr Orthop B1996;5:273–8.

10. Poul J, Garvie D, et al. Ultrasound examination ofneonate’s hip joints. J Pediatr Orthop B 1998;7:59–61.

11. Marks D, Clegg J, et al. Routine ultrasoundscreening neonatal hip instability. Can it abolishlate-presenting congenital dislocation of the hip.J Bone Joint Surg 1994;76:534–8.

12. Davids JR, Benson LJ, et al. Ultrasonography anddevelopmental dysplasia of the hip: a cost-benefitanalysis of three delivery systems. J Pediatr Orthop1995;15:325–9.

13. Clegg J, Bache CE, et al. Financial justification forroutine ultrasound screening of the neonatal hip. JBone Joint Surg Br 1999;81:852–7.

14. Exner GU, Frey E. [Hip dysplasia in infancy.Proton spin tomography and computerized tomo-graphy]. Orthopade 1997;26:59–66. (In German.)

15. Tegnander A, Terjesen T. Reliability of ultrasono-graphy in the follow-up of hip dysplasia in childrenabove 2 years of age. Acta Radiol 1999;40:619–24.

16. Court C, Carlioz H. Radiological study of severeproximal femoral focal deficiency. J Pediatr Orthop1997;17:520–4.

17. Kashiwagi N, Suzuki S, et al. Prediction ofreduction in developmental dysplasia of the hipby magnetic resonance imaging. J Pediatr Orthop1996;16:254–8.

18. Lin CJ, Romanus B, et al. Three-dimensional char-acteristics of cartilaginous and bony componentsof dysplastic hips in children: three-dimensionalcomputed tomography quantitative analysis. J PediatrOrthop 1997;17:152–7.

19. MacDonald J, Barrow S, et al. Imaging strategies inthe first 12 months after reduction of developmentaldislocation of the hip. J Pediatr Orthop B1995;4:95–9.

20. Champoux A, Bockers T, et al. Septic arthritisversus transient synovitis of the hip: the value ofscreening laboratory tests. Ann Emerg Med1992;21:1418–22.

21. Ranner G, Ebner F, et al. Magnetic resonanceimaging in children with acute hip pain. PediatrRadiol 1989;20:67–71.

22. Wilson D, Green D, et al. Arthrosonography of thepainful hip. Clin Radiol 1984;35:17–9.

23. Egund N, Wingstrand H, et al. Computed tomo-graphy and ultrasonography for diagnosis of hipjoint effusion in children. Acta Orthop Scand1986;57:211–5.

24. Harcke H, Grissom L. Pediatric hip sonography.Diagnosis and differential diagnosis. Radiol ClinNorth Am 1999;37:787–96.

25. Berman L, Fink A, et al. Technical note: identifyingand aspirating hip effusions. BJR 1995;68:306–10.

Imaging of children’s hips

185Imaging, Volume 14 (2002) Number 3

Page 8: Children's hip

26. Fink A, Berman L, et al. The irritable hip:immediate ultrasound guided aspiration and pre-vention of hospital admission. Arch Dis Child1995;72:110–3.

27. Zawin JK, Hoffer FA, et al. Joint effusion inchildren with an irritable hip: US diagnosis andaspiration. Radiology 1993;187:459–63.

28. Wirth T, LeQuesne G, et al. Ultrasonography inLegg-Calve-Perthes disease. Pediatr Radiol 1992;22:498–504.

29. Bosch R, Niedermeier C, et al. [Value of ultrasoundin differential diagnosis of pediatric hip jointeffusion (Perthes disease, C. fugax, epiphysiolysiscoapitis femoris]. Z Orthop Ihre Grenzgeb 1998;136:412–9.

30. Eggl H, Drekonja T, et al. Ultrasonography in thediagnosis of transient synovitis of the hip and Legg-Calve-Perthes disease. J Pediatr Orthop 1999;8:177–80.

31. Robben SG, Meradji M, et al. US of the painful hipin childhood: diagnostic value of cartilage thicken-ing and muscle atrophy in the detection of Perthesdisease. Radiology 1998;208:35–42.

32. Toby EB, Koman LA, et al. Magnetic resonanceimaging of pediatric hip disease. J Pediatr Orthop1985;5:665–71.

33. de Sanctis N, Rega AN, et al. Prognostic evaluationof Legg-Calve-Perthes disease by MRI. Part I: therole of physeal involvement. J Pediatr Orthop2000;20:455–62.

34. Hosokawa M, Kim WC, et al. Preliminary reporton usefulness of magnetic resonance imaging foroutcome prediction in early-stage Legg-Calve-Perthes disease. J Pediatr Orthop B 1999;8:161–4.

35. Minio Paluello GB, De Pellegrin M, et al.[Persistent coxalgia in the child. The value of magneticresonance]. Radiol Med (Torino) 1997;89:402–8.(InItalian.)

36. Ranner G. [Osteochondrosis deformans coxaejuvenilis (Legg-Calve-Perthes disease) in the MRtomogram: diagnosis and follow-up assessmentcorrelated with x-rays and skeletal scintigraphy].Rofo Fortschr Geb Rontgenstr Neuen BildgebVerfahr 1990;153:124–30. (In German.)

37. Schittich I, Gradinger R, et al. [Legg-Calve-Perthesdisease in the MRI: possibilities and limits]. Z OrthopIhre Grenzgeb 1990;128:404–10. (In German.)

38. Sebag G, Ducou Le Pointe H, et al. Dynamicgadolinium-enhanced subtraction MR imaging—asimple technique for the early diagnosis of Legg-Calve-Perthes disease: preliminary results. PediatrRadiol 1997;27:216–20.

39. Lahdes-Vasama TT, Lamminen AE, et al. MRI inlate sequelae of Perthes’ disease: imaging findingsand symptomatology in ten hips. Pediatr Radiol1996;26:640–5.

40. Mastantuono M, Milella PP, et al. [Role ofmagnetic resonance in the evaluation of the normaland osteochondrosis hip in early and late child-hood]. Radiol Med (Torino) 1997;94:571–8. (InItalian.)

41. Cowell H. The significance of early diagnosisand treatment of slipping of the capital femoralepiphyses. Clin Orthop 1966;48:89–94.

42. Boles C, el-Khoury G. Slipped capital femoralepiphysis. Radiographics 1997;17:809–23.

43. Kallio P, LeQuesne G, et al. Ultrasonography inslipped capital femoral epiphysis. J Bone Joint Surg1991;73:884–9.

44. Castriota-Scanderbeg A, Orsi E, et al.[Ultrasonography in the diagnosis and follow-upof hip pain in children]. Radiol Med (Torino)1993;86:808–14. (In Italian.)

45. Castriota-Scanderbeg A, Orsi E. Slipped capitalfemoral epiphysis: ultrasonographic findings.Skeletal Radiol 1993;22:191–3.

46. Shanker VS, Hashemi-Nejad A, et al. Slippedcapital femoral epiphysis: is the displacementalways posterior? J Pediatr Orthop B 2000;9:119–21.

47. Umans H, Liebling M, et al. Slipped capital femoralepiphysis: aphyseal lesion diagnosed by MRI, withradiographic and CT correlation. Skeletal Radiol1998;27:139–44.

48. Futami T, Suzuki S, et al. Sequential magneticresonance imaging in slipped capital femoralepiphysis: assessment of preslip in the contralateralhip. J Pediatr Orthop B 2001;10:298–303.

49. Konermann W, Gruber G, et al. [Standardizedsonographic examination of the hip joint].Ultraschall Med 2000;21:137–41. (In German.)

50. Marchal GJ, Van Holsbeeck MT, et al. Transientsynovitis of the hip in children: role of US.Radiology 1987;162:825–8.

51. de Pellegrin M, Fracassetti D, et al. [Coxitis fugax.The role of diagnostic imaging]. Orthopade1997;26:858–67. (In German.)

52. Thomas S, Tytherleigh-Strong G, et al. Adductormyositis as a cause of childhood hip pain. J PediatrOrthop B 2002;11:117–20.

53. Alexander JE, Seibert JJ, et al. A protocol of plainradiographs, hip ultrasound, and triple phase bonescans in the evaluation of the painful pediatric hip.Clin Pediatr (Phila) 1988;27:175–81.

54. Kearney SE, Carty H. Pelvic musculoskeletalinfection in infants—diagnostic difficulties andradiological features. Clin Radiol 1997;52:782–6.

55. Tran-Minh VA, Pracros JP, et al. Sonography ofthe hip and soft tissues of the thigh in children.Radiol Med (Torino) 1993;85(5 Suppl. 1):247–51.

56. Lamer S, Sebag GH. MRI and ultrasound inchildren with juvenile chronic arthritis. Eur J Radiol2000;33:85–93.

57. Eich GF, Halle F, et al. Juvenile chronic arthritis:imaging of the knees and hips before and afterintraarticular steroid injection. Pediatr Radiol1994;24:558–63.

58. Friedman S, Gruber MA. Ultrasonography of thehip in the evaluation of children with seronegativejuvenile rheumatoid arthritis. J Rheumatol2002;29:629–32.

59. Gennari JM, Merrot T, et al. X-ray transparencyinterpositions after reduction of traumatic disloca-tions of the hip in children. Eur J Pediatr Surg1996;6:288–93.

60. Macnicol MF. The Scottish incidence of traumaticdislocation of the hip in childhood. J PediatrOrthop B 2000;9:122–4.

61. Rubel IF, Kloen P, et al. MRI assessment of theposterior acetabular wall fracture in traumaticdislocation of the hip in children. Pediatr Radiol2002;32:435–9.

62. Futami T, Foster BK, et al. Magnetic resonanceimaging of growth plate injuries: the efficacy andindications for surgical procedures. Arch OrthopTrauma Surg 2000;120:390–6.

63. Pelsser V, Cardinal E, et al. Extraarticular snappinghip: sonographic findings. AJR 2001;176:67–73.

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64. Wunderbaldinger P, Bremer C, et al. Efficientradiological assessment of the internal snappinghip syndrome. Eur Radiol 2001;11:1743–7.

65. Choi YS, Lee SM, et al. Dynamic sonography ofexternal snapping hip syndrome. J Ultrasound Med2002;21:753–8.

66. Ghebontni L, Roger B, et al. MR arthrographyof the hip: normal intra-articular structures andcommon disorders. Eur Radiol 2000;10:83–8.

67. Grainger AJ, Elliott JM, et al. Direct MRarthrography: a review of current use. Clin Radiol2000;55:163–76.

68. Erb RE. Current concepts in imaging the adult hip.Clin Sport Med 2001;20:661–96.

69. Petersilge CA. MR arthrography for evaluation ofthe acetabular labrum. Skeletal Radiol 2001;30:423–30.

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