HTHSCI 2F03 Lecture Notes - Lecture 9: Transient Synovitis, Brachial Artery, Femoral Head

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The Limping Child
Aetiology
DDH
Transient synovitis
Septic arthritis
Perthes’
Slipped Capital Femoral Epiphyses
JIA / Still’s Disease
DDH
Congenital hip joint deformity in which the femoral head
is or can be completely / partially displaced.
Epidemiology
Incidence: 1/1000
Sex: F>M
Predisposing Factors
FH
Breach presentation
Oligohydramnios
Presentation
Screening
Asymmetric skin folds
Limp / abnormal gait
Ix
US is v. specific
Mx: maintain abduction
Double nappies
Pavlik harness
Plaster hip spica
Open reduction: derotation varus osteotomy
Transient Synovitis: Irritable Hip
Commonest cause of acute hip pain in children
Presentation
2-12yrs
Sudden onset hip pain / limp
Often following or with viral infection
Not systemically unwell
Ix
PMN and ESR/CRP are normal
-ve blood cultures
May need joint aspiration and culture
Mx
Rest and analgesia
Settles over 2-3d
Perthes’ Disease
Osteochondritis of the femoral head 2O to AVN.
Epidemiology
4-10yrs
M>F=5:1
Presentation
Insidious onset
Hip pain initially, then painless
10-20% bilateral
Ix
X-rays normal initially
density of femoral head
Becomes fragmented and irregular
Flattening and sclerosis
Bone scan is useful
Mx
Detected early and < half femoral head affected
Bed rest and traction
More severe
Maintain hip in abduction c
¯ plaster
Femoral or pelvic osteotomy
Slipped Capital Femoral Epiphysis
Postero-inferior displacement of femoral head epiphysis
10-15yrs
Two main groups
Fat and sexually underdeveloped
Tall and thin
Presentation
Slip may be acute, chronic or acute-on-chronic
Acute
Groin pain
Shortened, externally rotated leg
All movements painful
20% bilateral
Ix
Confirm Dx by x-ray
Mx
Acute: reduce and pin epiphysis
Chronic: in situ pinning
Epiphyseal reduction risks AVN
Complications
Chondrolysis: breakdown of articular cartilage
risk c
¯ surgery
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Acute Osteomyelitis
Pathophysiology
Source: local or haematogenous.
Organisms
Staph
Strep
E. coli
Pseudomonas
Salmonella (in SCD)
RFs
Vascular disease
Trauma
SCD
Immunosuppression (e.g. DM)
Children
Rich blood supply to growth plate
usually affects metaphysis
Symptoms and Signs
Pain, tenderness, erythema, warmth, ROM
Effusion in neighbouring joints
Signs of systemic infection
Investigations
ESR/CRP, WCC
+ve blood cultures in 60%
X-ray:
Changes take 10-14d
Haziness + bone density
Sub-periosteal reaction
Sequestrum and involucrum
MRI is sensitive and specific
Management
IV Abx: Vanc + cefotaxime until MCS known
Drain abscess and remove sequestra
Analgesia
Septic Arthritis
Pathophysiology
Source: local or haematogenous.
Organisms
Staph: 60%
Streps
Gonococcus
Gm-ve bacilli
RFs
Joint disease (e.g. RA)
CRF
Immunosuppression (e.g. DM)
Prosthetic joints
Symptoms
Acutely inflamed tender, swollen joint.
ROM
Systemically unwell
Investigations
Joint aspiration for MCS
↑↑ WCC (e.g. >50,000/mm3) : mostly PMN
ESR/CRP, WCC, Blood cultures
X-ray
Management
IV Abx: vanc + cefotaxime
Consider joint washout under GA
Splint joint
Physiotherapy after infection resolved
Complications
Osteomyelitis
Arthritis
Ankylosis: fusion
Differential
Crystal arthropathy
Reactive arthritis
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Bone Tumours
Bony Mets
Commonest bone tumours
Bronchus, thyroid, breast, kidney and prostate
Usually radiolucent (except prostate which is sclerotic)
Usually axial skeleton (contains red marrow)
Present with pain or pathological #
Path # internal fixation
Pain radiotherapy
Tumour-like Non-neoplastic Conditions
Lesion Clinical Features Location X-ray
Fibrous Dysplasia 0-30
F>M
# risk
McCune Albright’s
- Polyostotic fibrous dysplasia
- Precocious puberty (females)
- Café-au-lait spots
Long bones
Ribs
Skull
Usually mono-ostotic
“Ground Glass” lytic lesion
Shepherds crook deformity of prox. femur
Simple bone cyst <20
Lump migrates down shaft
from original growth plate site.
Prox metaphysis of
humerus or femur
Well-defined lytic lesion
Cortex can fall into cyst “fallen
fragment”
Aneurysmal bone cyst <30yrs
Pain
MRI shows multiple fluid levels
Fibrous cortical defect
and non-ossifying
fibroma
Children
Non-painful, benign
Spontaneously regress
Dist femur
Prox tibia
Often multiple
Benign Cartilaginous Neoplasms
Lesion Clinical Features Location X-ray
Osteochondroma
(exostosis)
10-20
M>F = 3:1
Commonest benign bone tumour
May be related to previous trauma
Knee Cartilage-capped bony outgrowth
Enchondroma /
Chondromas
10-40
M=F
Ollier Disease = multiple enchondromas
Maffucci Syn = Enchondromatosis + multiple
soft-tissue haemangiomas
Multiple enchondromas have risk of malignant
transformation
Hands
Feet
O sign
- Oval lucencies c
¯ radiodense rim
Endosteal scalloping
Chondroblastoma 10-20
M>F = 2:1
Epiphysis
Knee
Radiolucent with sclerotic border
Malignant Cartilaginous Neoplasms
Lesion Clinical Features Location X-ray
Chondrosarcoma >40
Pain + lump
Arise de novo or from chondromas
70% 5ys
Pelvis
Axial skeleton
Lytic lesion
Fluffy “popcorn calcification”
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Document Summary

Congenital hip joint deformity in which the femoral head is or can be completely / partially displaced. Commonest cause of acute hip pain in children. Osteochondritis of the femoral head 2o to avn. Detected early and < half femoral head affected. Slip may be acute, chronic or acute-on-chronic. Iv abx: vanc + cefotaxime until mcs known. Wcc (e. g. >50,000/mm3) : mostly pmn. Cortex can fall into cyst fallen fragment . Usually radiolucent (except prostate which is sclerotic) Lump migrates down shaft from original growth plate site. Lytic lesion c central nidus and sclerotic rim. Roots leave vertebral column between scalenus anterior and medius. Divisions occur under the clavicle, medial to coracoid process. Plexus has intimate relationship c subclavian and brachial arteries. Median n. is formed anterior to brachial artery. Direct: e. g. shoulder girdle #, penetrating or iatrogenic injury. Leffert classification: open, closed, supraclavicular, infraclavicular, radiation-induced, obstetric, upper, lower, mixed. Loss of extension of cmc joints (finger drop)

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