Orthopaedics Flashcards

1
Q

Commonest malignant primary bone tumour

A

Oseosarcoma

50% around the knee

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2
Q

Complications of colle’s fracture

A

Compression on median nerve

Rupture of extensor pollicis longus tendon

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3
Q

Imaging for scaphoid fractures

A

If first x-ray NAD

Fix for two weeks then re-x-ray

If still NAD –> MRI

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4
Q

Lasègue’s straight leg raise test

A

Increases tension along the sciatic nerve (L5 and S1 nerve roots)

97% sensitive for disc prolapse

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5
Q

Intrinsic muscle wasting of the hand

A

Ulnar nerve palsy T1

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6
Q

Thenar wasting

A

Median nerve palsy C8

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7
Q

Hypothenar wasting

A

Ulnar nerve palsy T1

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8
Q

Medial epicondylitis

A

Golfer’s elbow

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9
Q

Lateral epicomdylitis

A

Tennis elbow

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10
Q

Morton’s neuroma

A

Thickening of the tissue that surrounds the digital nerve leading to the toes as the nerve passes under the ligament connecting the metatarsals in the forefoot

It is most frequent between the third and fourth toes.

A neuroma presents with burning pain in the ball of the foot that radiates to the involved toes.

Palpate in the web space between the symptomatic toes for a mass.

Compression of the metatarsals may elicit a ‘click’ betwee the bones (Molders’ click).

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11
Q

Sites of tendon injury with age

A

Adolescents: tendon insertions

Adults: musculotendinous junction

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12
Q

Grading ligamentous injuries 0-3

A

0 = Normal ligament

1 No increase in joint laxity but there is tenderness around the injured ligament

2 Partial disruption of the ligament fibres with increased joint laxity, and a soft end point

3 Complete disruption of the ligament; there is a marked increase in joint laxity with no end point clinically

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13
Q

Management of ligamentous injuries

A

Grade 1 + 2: splinting, anaglesia and fraded mobilisation

Garde 3: surgical repair

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14
Q

Posterior impingement of the ankle and tendinopathy of the flexor hallucis longus tendon

A

Ballet dancers

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15
Q

Ottawa ankle rules

A

Bone tenderness along the distal 6 cm of the posterior margin or at the tip of the lateral malleolus

Bone tenderness along the distal 6 cm of the posterior margin or at the tip of the medial malleolus

Inability to bear weight at the time of the accident or at the time of examination

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16
Q

Cervical lordosis

A

35-45 ‘

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17
Q

Lumbar lordosis

A

40 - 80’

Mostly occurs L4 - S1

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18
Q

Thoracic kyphosis

A

20 - 50’ (mean 35’)

Increases with age

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19
Q

Radicular artery of Adamkiewicz

A

Largest anterior segmental medullary artery

Arises left posterior intercostal artery at the level of the T9 - T12 intercostal artery, which branches from the aorta, and supplies the lower two thirds of the spinal cord via the anterior spinal artery

Ligation –> ischaemia of the spinal column

During anterior approaches to the spine, segmental division is performed to avoid ligating this influental vessel

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20
Q

Cauda equina

A

Low back pain

Uni- or bilateral sciatica

Saddle anaesthesia

Motor weakness in the lower extremities

Variable rectal and urinary symptoms

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21
Q

Lasègue’s sign

A

Denotes radicular pain aggravated by ankle dorsiflexion during straight leg raise

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22
Q

Provocative discography

A

3.5 mL of radio-opaque contrast agent is injected into the disc

The contrast pattern will allow the discrimination of different degrees of disc degeneration; cottonball or lobular would be considered normal

Whereas irregular, fissured or ruptured would be considered degenerate

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23
Q

Indication for surgical intervention in cervical radiculopathy

A

Intractible pain

OR

Functional neurological deficit

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24
Q

Surgical management of cervical radiculopathy

A

Anterior cervical discectomy and fusion (using a cage packed with bone graft and plate)

Cervical total disc replacement

Posterior laminoforaminotomy

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25
Cervical myelopathy
LMN signs AT level of lesion UMN signs below level of lesion
26
Commonest cause of cauda equina syndrome
Massive central lumbar disc protrusion at L4/5
27
Lumb disc herniation
90% at L4/L5 or L5/S1 levels Posterolateral disc protrusion will affect the traversing root, e.g. an L4/5 disc protrusion will affect the L5 nerve root. Far-lateral disc protrusion (extraforaminal) will affect the exiting nerve root, e.g. a far-lateral L5/S1 disc protrusion will affect the L5 nerve root
28
Spinal stenosis
Classic symptoms: back, buttock, thigh and calf pain LIGAMENTUM FLAVUM Provoked by walking and extended posture Relieved by flexed posture Symptoms progress in up to one-third of untreated patients
29
Spondylolysis
Unilateral or bilateral defect in the pars interarticularis without vertebral slippage Incidence in athletic population 15–47% May be completely asymptomatic/incidental finding on radiograph Difficult to image, but MRI proving more useful Conservative treatment: activity modification, antilordotic brace Surgical treatment: direct repair preserving motion or spinal fusion if associated disc degeneration
30
Spondylolisthesis
Forward slippage of the vertebral body caused by a break in in the continuity of pars interarticularis Wiltse classification of spondylolisthesis identifies the CAUSE = 6 types Meyerding classification grades severity = 4 grades Low grade slip I - II --> fusion-in-situ High grade slips III - IV--> decompression and fusion
31
Commonest metatastic malignancy to spine
Breast 21% Lung 14%
32
Benign primary spine tumours
Osteoid osteoma Osteoblastoma Chondroma Chondroblastoma Chondromyoixod fibroma Giant cell tumous Haemangioma Lymphangioma Lipoma Benign tumours tend to occur in the posterior elements
33
Intermediate spinal pimaries
Aggressive osteoblastoma Haemangiopericytoma Haemangioendothelioma Chordoma
34
Malignant spinal pimaries
Osteosarcoma Chondrosarcoma Ewing’s sarcoma Neuroectodermal tumours Malignant lymphoma Myeloma Angiosarcoma Fibrosarcoma Liposarcoma Malignant tumours tend to involve the entire vertebral column
35
Neurofibroma
Benign tumours arising from the nerve sheath Three types: -Cutaneous -Spinal -Plexiform 90% of cases they present as solitary lesions, Multiple = patients with neurofibromatosis type 1 (NF1), -autosomal dominant
36
Neurofibromatosis Type 1
Referred to as peripheral neurofibromatosis or von Recklinghausen disease 1 in 3000 Diagnosis of NF1 (2 or more of the following): -At least 6 cafe au lait spots >5mm pre-puberty -At least 6 cafe au lait spots >15mm post-puberty -Two or more neurofibromas (any type) -Presence of plexiform neurofibroma -Multiple freckles in the axillary or inguinal regions, -Distinctive bone abnormality involving the eye socket or arm/leg bones -Optic glioma in the brain -Two or more Lisch nodules in the eye, -Parent, sibling or child with NF1
37
Neurofibromatosis Type II
Central 1 in 40,000 Schwannomas on both 8th cranial (vestibular) nerves Parent, sibling or child with NF2 plus: -One vestibular schwannoma in a person less than 30 years of age -Any two of the following: meningioma, glioma, schwannoma, juvenile cataracts
38
Epidural abscess
Surgical emergency Majority of cases occur within the thoracic spine. Without treatment --> neurological deficit including paralysis may develop.
39
Indications for surgery in atlanto-axis subluxation in rheumatoid arthritis
AAS with a PADI of 14 mm or less AAS with at least 5 mm of basilar invagination Subaxial subluxation with a sagittal canal diameter of 14 mm or less (PADI= posterior atlantodental interval)
40
Cobb angle of 10° or more
= Scoliosis
41
Early onset idiopathic scoliosis
Cause disruption to lug development After 8 years, late onset scoliosis, the alveoli are developed Early onset may cause cor pulmonale and RHF
42
Management of idiopathic scoliosis
Idiopathic curves of less than 25° are monitored with clinical and radiographic examination In growing children (premenarchal) with curves between 20° and 29°, a brace may be indicated. Bracing is used to prevent curve progression Curves beyond 45° are not amenable to brace treatment. Surgery in the form of corrective instrumentation and spinal fusion is indicated for curve progression beyond 40°, truncal imbalance and unacceptable cosmesis. During surgery, continuous spinal cord monitoring is used in the form of somatosensory evoked potentials (SSEP), motor-evoked potentials (MEP) and free-run and stimulated electromyographic (EMG) activity to minimise the risk of neurological damage. The risk of neurological injury is 0.4% (1 in 250).
43
Stener lesion
Occurs due to gamekeepers thumb Aponeurosis of ABductor pollicis longus interposed between the ruptured ulnar collateral ligament (UCL) of the thumb and its site of insertion at the base of the proximal phalanx No longer in contact with its insertion site, the UCL cannot spontaneously heal Mx: surgicalk attachment
44
Scheuermann's kyphosis
Wedging og T7 - T10 vertebrae Apical pain and lower back pain --> attempts by lumbar musculature to compensate for the thoracic hyperkyphosis Mx Physiotherapy Bracing in skeletally immature Surgical: -Pain (apical or low back pain produced by compensatory hyperlordosis) -Progressive deformity greater than 70°, -Unacceptable cosmesis and neurological and/or cardiopulmonary compromise Anterior release followed by posterior correction and fusion. Posterior chevron osteotomies carried out at the time of posterior instrumentation may prevent the need for the initial anterior release
45
Diastematomyelia
An abnormal bony or cartilaginous spur projecting across the middle of the vertebral canal --> dividing the dural tube and spinal cord in two Between 50% and 70% of patients are seen to have a skin naevus, dimple or hairy patch when the spine is examined
46
Management of osteoporotic spinal fractures
Providing no neural comprimise Bed rest Analgesia If painful --> Kyphoplasty -->Vertebroplasty
47
Sprengel's shoulder
Abnormal descent of the scapular from its embryonic mid-cervical position High, small, rotated scapular that remains attached to the cervical spine by a: -bony bar, or -fibrous band, or -omovertebral body
48
Klippel-Feil syndrome
Congenital abnormality involving fusion of at least two cervical vertebrae --> short neck and reduced mobility, causes apparent low hair-line
49
Risk factors for frozen shoulder
Diabetes Cardiovascular disease Thyroid disease Female gender Age
50
Treatment of calcific tendonitis
Acute pain with restricted movement around the shoulder due to subacromial calcific deposits BUT external rotation possible Tx: Corticosteroid injections Barbotage: aspiration and flushing Surgical decompression if persistent
51
Changes in rheumatoid arthritis
Osteoporosis Destruction of articular cartilage Synovial proliferation Pannus formation
52
Rupture of the long head of the biceps
Tends to be proximal tendon rupture in elderly patients due to abrasion under the anterior acromion --> bulge appears in arm -->sometimes pain of biceps tendonitis is relived by rupture In elderly it doesn't alter function --> conservative management
53
Types of shoulder instability
Traumatic Atraumatic Habitual
54
Types of shoulder instability
Traumatic -Surgery Atraumatic -Surgery Habitual -Not for surgery
55
Bankart's lesion
Detachment of the anteroinferior labrum
56
Hill-Sach's lesion
Damage to the humeral head Cortical depression on posterolateral humeral head
57
Management of traumatic recurrent shoulder instability
Repair of labrum Tightening of anterior capsule +/- graft of Hill-Sachs
58
Posterior shoulder dislocation
Forced internal rotation -Electrocution -Seizure -Restraint
59
Rheumatoid elbow
Radial head excision Elbow arthroplasty
60
Points of ulnar compression
Within the cubital tunnel (behind medial epicondyle) Junction of arcade of Struthers Medial intermuscular septum as nerve passes into posterior compartment of distal humerus Between heads of flexor carpi ulnaris
61
Froment's sign
Weakness of adductor pollicis = ulnar nerve palsy
62
Edinburgh position of safety
Hand splinting position to prevent collateral ligament shortening and deformity during times of immobiliation = Wrist extension =MCP flexion =IPJ extension
63
Thumb ulnar collateral ligament injury
= Gamekeepers thumb Chronic overuse --> stretching of ulnar collateral ligament of thumb Skier's thumb = forceful abduction causing acute tear Surgical Mx: pollicis abbductor tendon slips between two ends and prevents healing
64
Triangular fibrocartilage complex injuries
Triangular fibrocartilage complex: -Ulnocarpal ligaments -Extensor carpi ulnaris tendon -Meniscus-like structure between distal ulna and carpus Stabilises distal radio-ulnar joint Injury --> ulna wrist pain and instability Mx: arthroscopic / open repair Debridement if chronic damage
65
Felon
Abscess of specialised fibrous septae in finger pulp Can cause DIP osteomyelitis Mx: I&D
66
Paronchyia
Nail bed infection Incision, drainage and Abx +/- partial removal of nail to allow drainage
67
Flexor tendon sheath infection
Kanavel's cardinal signs -held in flexion -swelling over tendon and digit -tender -pain on passive extension Mx: tendon sheath irrigation and IV Abx Untreated: adhesions, necrosis, +/- proximal spread
68
Hand signs of Rheumatoid
Boutonniere Swan-neck Flexor tendon synovitis Radial deviation of wrist + prominent ulnar head Flexion, subluxation and ulnar deviation of MCPs
69
Dupuytren's
Autosomal dominant Palmar nodules Skin puckering Cords Flexion contractures Garrods knuckle pads over dorsal of PIPs Associated with: Smoking Trauma Epilepsy AIDS Hypothyroidism Alcohol liver cirrhosis Mx: when patient can't put hand flat on table OR Flexion develops in the PIP joint --> surgery Z-plasties Digital nerves at-risk Proceed to amputation if finger restricting useful movements
70
Trigger finger
Tendon size mismatch between flexor tendon sheath pulley A1 and size of flexor tendon --> locking / snapping of finger --> pain Mx: Corticosteroid injection Proceed to pulley release In thumb in children --> resolved spontaneosuly
71
De Quervain's
Tenosynovitis of abductor pollicis longus and extensor pollicis brevis within first dorsal extensor compartment 1st EC Associated: Female patients during pregnancy (New mother's wrist) Inflammatory arthritis Test: Finkelstein's
72
Associations with carpal tunnel syndrome
Majority idiopathic BUT... Diabetes Thyroid disease Alcoholism Amyloidosis Inflammatory arthritis Pregnancy Obesity
73
Tests for carpal tunnel syndrome
Phalen's test: flexion of wrist Tinnel's test: tap on carpal tunnel Durkin's test: press on carpal tunnel
74
Management of carpal tunnel syndrome
Night splinting of wrist in extension Surgical decompression -Transverse carpal ligament
75
Guyon's tunnel syndrome
Ulnar nerve compression in Guyon's tunnel Tingling and numbness in little and ring finger Hypothenar wasting Dorsal branches don't pass through so dorsal sensation intact Causes: Ganglion Ulnar artery aneurysm Hook of hamate fracture
76
Kienbock's disease
Idiopathic avascular necrosis of the lunate
77
Preiser's disease
Idiopathic avascular necrosis of the scaphoid
78
Blood supply to femoral head
Retinacular branches of medial circumflex femoral artery Small contribution from ligament teres
79
Causes of avascular necrosis of the femoral head
Avascular of the femoral head can be idiopathic (Perthe's) or secondary --> collapse of femoral head -->secondary osteoarthritis Causes: -Sickle cell disease -Haemoglobinopathies -Hypercoaguable states (protein C and S deficiency) -Caisson disease (the bends in divers) -Hyperlipidaemia -SLE -Gaucher's disease -Antiphospholipid syndrome -Radiotherapy -Chemotherapy -HIV -Steroids -Chronic liver disease -Alcoholism
80
Presentation of AVN of femoral head
Men aged 35-45 Bilateral in >50% Asymptomatic initially Ache in groin Limp Limitation of movement
81
Radiographic changes in avascular necrosis of the femoral head
Initially normal, request an MRI Early: sclerosis Crescent sign --> subchondral bone resorption Flattening --> femoral collapse Graded I - IV
82
Management of AVN of femoral head
Pre-collapsed stage --> surgical decompression using core decompression +/- inserting vascular bone graft Collapsed --> femoral osteotomy to shift WB or replacement
83
Causes of secondary osteoarthritis of hip
Trauma Avascular necrosis / Perthe's Slipped capital femoral epiphysis Dysplasia Inflammatory arthtropathy = Rheumatoid Developmental dysplasia of hip Septic arthritis Femeroaectabular impingement
84
Posterior approach to hip replacement
Along the fibres of gluteus maximus, dividing short external rotators of the hip sciatic nerve at risk
85
Anterolateral approach to hip replacement
=Hardinge Parts of the gluteus medius and minimus are reflected off the greater trochanter superior gluteal at risk
86
Medial meniscus tears
Three times more common than lateral meniscus tears Outer third of the meniscus is vascular and so tears can be repaired with the prospect of healing
87
Bundles of the ACL
Two bundles Anteromedial bundle: tight in flexion Posterolateral bundle: tight in extension
88
Bundles of the PCL
Two bundles: Anterolateral bundle: tight in flexion Posteromedial bundle: tight in extension
89
Lisfranc's Injury
Disruption to the cornerstone second metatarsal 2nd metatarsal is recessive in relation to 1st and 3rd --> Loss of transverse arch and flat foot
90
Superficial posterior compartment of leg
Gastrocnemius Soleus Plantaris
91
Deep posterior compartment of leg
Tibialis posterior Flexor digotorium longus Flexor hallucis longus
92
Lateral compartment of leg
Peroneus longus Peroneus brevis
93
Anterior compartment of leg
Tibialis anterior Extensor digitorum longus Extensor hallucis longus Peroneus tertius
94
Morton's neuroma
Pain in the second or third web space Compression of common digital nerve between third and fourth metatarsal --> pain Usually secondary to other foot deformities
95
Freiberg's disease
Avascular necrosis of epiphysis of metatarsal --> re-shaping osteotomy
96
Management of Charcot
Immediate off-loading and casting to correct deformity
97
Plasmacytoma
= solitary mass of myeloma
98
Osteosarcoma
Osteogenic tumours Two peaks: Adolescence Second in elderly patients with Paget's disease or post radiotherapy treatment
99
Onion-skinning
= Ewing's sarcoma
100
Familial conditions with high risk of bone and cartilage cancers
Maffuci syndrome -Enchondromatosis and soft tissue angiomas Ollier disease -Enchondromatosis Familial retinoblastoma syndrome
101
Ollier disease
Nonhereditary sporadic disorder where intraosseous benign cartilaginous tumors (enchondroma) develop close to growth plate cartilage
102
Maffuci syndrome
Maffucci syndrome is a sporadic disease characterized by the presence of multiple enchondromas associated with multiple cavernous hemangioma and phlebolith.
103
Conditions associated with moderate risk of cancerous transformation
Hereditary multiple exocytoses Polyostotic Paget's Radiation osteitis
104
Low risk of malignant change
Osteomyelitis Osteonecrosis Fibrous dysplasia Osteogenesis imperfecta Osteoblastoma Chondroblastoma
105
Batson's venous plexus
Retroperitoneal veins with no valves that allow haematgenous mets to the spine + proximal long bones
106
Sclerotic bone mets
Pancreatic metastasis
107
Osteoid osteoma
Bening bone-forming lesion -Usually occur in children and adolescents Small but very painful Pain occurs at night Responds to NSAIDs Commonly in proximal femur, and cause a dense cortical reaction in the centre of which is a nidus
108
Osteomablastoma
Larger version of osteoid osteoma - still benign >2cm More aggressive counterpart of osteoid osteoma that more typically occurs in the spine.
109
Osteosarcoma
Malignant bone-forming tumour Most common site: distal femur Classification: -Sclerotic -Chondroblastic -Telangiectatic Usually intraosseous
110
Osteoid tumours
Osteoid osteoma – small, painful; produce dense cortical reaction Osteoblastoma – larger and more aggressive than osteoid osteoma Osteosarcoma – malignant; commonest in lower femur and upper tibia
111
Osteochondroma
Benign cartilage-capped bony projection Continuity between cortex of bone and frowth - characteristic finding Bony projection always grows away from the joint towards the diaphyseal region of the bone. Osteochondromas can be pedunculated with a stalk or sessile (without a stalk) Usually solitary, but some patients have multiple osteochondromas (hereditary multiple exostoses, autosomal dominant inheritance) Cause compressive symptoms: nerve impingement, vascular pseudoaneurysm, fracture and infarction
112
Hereditary multiple exostoses
Autosomal dominant
113
Enchondroma
Benign cartilagenous neoplasm Within the intramedullary cavity of bone 50% are in the hands and feet: enchondromas are the most common bone tumours in the hand. A Pain, swelling or pathological fracture, many are asymptomatic Patchy calcification, expansion and scalloping can be visible on radiographs Ollier disease is a developmental condition characterised by multiple enchondromas Maffucci syndrome, multiple enchondromas are associated with multiple angiomas Malignant transformation to chondrosarcoma can occur in approximately 20% of patients with Ollier disease and is almost inevitable in patients with Maffucci syndrome.
114
Patchy calcification, expansion and scalloping can be visible on radiographs
Enchondroma
115
Chrondroblastoma
Benign cartilage-producing tumour Occurs in EPIPHYSES of bones in CHILDREN Commonly knee Presents: severe pain and knee effusion Radiograph often missed lytic lesion in centre of epiphyses -Isotope bone scan can help identify the lesion
116
Chondrosarcoma
Malignant tumour with cartilagenous differentiation Low- grade --> aggressive Pain + welling Many arise from enchondromas or osteochondromas Clear cell chondrosarcoma is a rare form of chondrosarcoma that occurs in the epiphysis
117
Tumours of cartilage differentiation
Osteochondroma – cartilage capped; grows away from physis Enchondroma – inside bone; commonest in hands and feet Chondroblastoma – in epiphyses of adolescents Chondrosarcoma – of varying malignancy
118
Eosinophilic granuloma
Eosinophilic granuloma is a rare neoplasm of Langerhans cells Unifocal (eosinophilic granuloma) Multifocal (Hand–Schuller–Christian disease) Disseminated (Letterer–Siwe disease). --> Skull and the diaphyses of long bone In the spine it can present with collapse, known as vertebra plana Radiographs can appear aggressive and similar to Ewing’s sarcoma -often expansion and a ground glass appearance, sometimes with cystic change
119
Ewing's Sarcoma
Malignant round cell sarcoma T11:22 Arises diaphysis long bone or pelvis Painful mass and may have systemic symptoms including fever, anaemia and increased erythrocyte sedimentation rate (ESR) Radiologically the bone appears moth-eaten and may show an ‘onion-skin’ periosteal reaction
120
Bone tumours misc
Simple bone cyst – proximal long bones of children Aneurysmal bone cyst – more aggressive, expanding Giant cell tumour – found in epiphyses around the knee Fibrous dysplasia – may be multiple; long bones, ribs and skull Ewing’s – round cell sarcoma; patients may have fever and anaemia
121
Enneking staging system
Staging primary bone cancers If breached cortex = 2B
122
Trojani system
Staging for malignant sodt tissue tumours Based on tumour differentiation, mitotic count and tumour necrosis,
123
Relief with non-steroidal anti-inflammatory drugs may suggest
an osteoid osteoma
124
Red flags for soft mass
Painful Increasing in size More than 5 cm in diameter
125
Biopsy for ?sarcoma
Only biopsy once staging is completed Biopsy should be performed at the institution undertaking the main surgery Imaging-guided biopsy is more reliable he biopsy track must be excised at definitive surgery Jamshidi needles for bone, Trucut needles for soft tissues
126
CT-guided thermocoagulation
Used in treatment of osteoid osteoma Many recgress spontaneously
127
Neoadjuvant chemotherapy
Pre-op chemotherapy used for: -Osteosarcoma -Ewing's sarcoma
128
Insensitive to radio or chemotherapy
Chondrosarcomas
129
Mirel's scoring system
Used to predict risk of pathological fracture Larger, more painful, lytic lesions carry a higher risk Lower limb higher risk vs upper limb
130
Soft tissue sarcomas
Complete excision with biopsy tract Not senitive to chemotherapy Pre-op and post-op radiotherapy can be useful but can impair wound healing
131
Involucrum
Pathological feature of osteomyelitis in which new bone is constructed around dead bone forming many sinuses
132
Debridement, antibiotics and implant retention, ‘DAIR’
Can only be undertaken if the prosthesis is well-fixed The surrounding infected soft tissue and bone must be fully excised and modular components exchanged This cannot be achieved by arthroscopic surgery Good soft tissue cover is essential. Following debridement, the patient is treated with long-term antibiotics (frequently 6 weeks of intravenous therapy followed by 6 months or more of oral antibiotics). Prolonged infection-free intervals will be achieved in 80% of patients but success with this strategy may be lower in infections caused by Staphylococcus aureus.
133
Two-stage joint revision surgery
Thorough excision is undertaken and all cement and loose foreign material is removed. An antibiotic-impregnated spacer may be implanted (which may be articulating) This is a temporary measure and cannot withstand full weight bearing. The patient is treated with oral or intravenous antibiotics, most commonly for 6 weeks. New prosthesis is implanted after the course of antibiotics has been completed. Rerevision surgery for infection has a higher failure rate than a first revision, and so early referral to a specialist centre should be considered.
134
Single-stage joint revision surgery
Removal and reimplantation are undertaken in the same operating session. Healthy soft tissues around the new implant are essential to prevent reinfection. Some centres consider single-stage revisions when less florid signs of infection are present (i.e. absence of collections or sinus tracts), or for frail patients for whom the risk of a second operation is higher. There are no adequate trial data comparing outcomes with the two-stage approach.
135
Commonest site of acute osteomyelitis in adults
Vertebral column Children: long bones
136
Cierny and Mader classification
Classification for chronic osteomyelitis Four stages of infection Stage 1: medullary -just cancellous bone -ream bone and pack with Abx pellets Stage 2: superficial -Only the cortical bone is involved and this requires excision. - follows skin ulceration and there may be large skin defects which require complete excision and local or free muscle flaps Stage 3: localised -limited area of dead cortical bone with medullary infection. -staged reconstruction after excisio n Stage 4: diffuse -Involves the entire circumference of the bone and surrounding soft tissue -All infected non-unions are Stage 4. -Resection must be segmental and stabilisation in an external fixator will be required. Reconstruction will involve the introduction of new bone and healthy soft tissue -Ilizarov method, which uses distraction osteogenesis to fill bone defects Three host groups A- C A, no active concurrent disease B, compromised host C,severe comorbidity preventing surgery
137
Stages of chronic osteomyelitis
Stage 1: medullary Stage 2: superficial Stage 3: localised Stage 4: diffuse
138
Occurence of congenital limb abnormalities
Usually occur within 2 motnhs of fertilisation The upper limb bud forms on the lateral wall of the embryo 4 weeks after fertilisation, followed promptly by the lower limb bud AER controls proximal to distal differentiation and interdigital necrosis ZPA directs posterior to anterior differentiation Wnt influences dorsal to ventral differentiation
139
Heuter-Volkmann principles
Compressibe forces inhibit growth Tensile forces stimulate growth
140
Wolff's law
Bone deposition and resorption depend on the stresses applied
141
Apical ectodermal ridge
Guides mesordermal proliferation in the progress zone in proximal --> distal direction Controls digit formation
142
Zone of polarising activity
Mesodermal zone of polarising activity directs anteroposterior limb development via the sonic hedgehog protein
143
Ectodermal driven wingless- type (Wnt) signalling centre
Ectodermal driven wingless- type (Wnt) signalling centre develops dorsoventral axis configuration and limb alignment.
144
Cause of persistent in-toeing gait
Femur/hip: Persistent femoral neck anteversion Tibia: Internal tibial torsion Foot: Metatarsus adductus
145
Internal tibial torsion
Internal tibial torsion is assessed by the thigh–foot angle Commonly associated with physiological tibia vara in infants Spontaneous correction can be expected by age 4, as the tibia also rotates as it grows.
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Normal variants of early gait
Children’s legs are often bowed until age 2 years and then knock-kneed until age 6 or 7 years Neuromuscular pathology must be excluded in toe walkers, particularly when the onset is late Intoeing or extoeing may be caused by excessive femoral or tibial torsion or foot deformity Flexible, pain-free flat feet do not need treatment
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Flat foot
Flexible vs rigid Flexible: On tiptoe the arch is restored and the heel corrects into varus; subtalar joint movements are full and pain free Rigid: On tiptoe the arch fails to return and the heel remains in valgus; subtalar joint movements are restricted and often painful =inflammation or a tarsal coalition (calcaneonavicular bar)
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Achondroplasia
Gain in function mutation in fibroblast growth factor receptor 3 (FGFR3) Short arm chromosome 4 Autosomal dominant Disproportionate short stature where the limbs are shorter than the trunk Radiograph features: -Splaying metaphysis -Over-long fibula -Slight bowing -Horzontal acetabulum -Square pelvic wings Underdevelopment of the foramen magnum and spinal stenosis can cause neurological difficulties
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McCune Albright’s
Precoious puverty Cafe-au-lait spots Fibrous dysplasia
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ground glass’ appearance
Fibrous dysplasia
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Developmental dysplasia of the hip screenig test
DDH defines the spectrum of hip instability, ranging from the hip that is in joint but has a shallow (dysplastic) acetabulum 'pushed out’ (Barlow positive) to the dislocated hip Irreducible (Ortolani negative).
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Management of DDH
Many hips that are unstable in the first few days/weeks of life do not need treatment as they improve spontaneously Up to age 4–6 months, a harness or splint is effective treatment In older babies, closed reduction is often possible and preferable to an open reduction For failed closed treatment, open surgical reduction is required
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Avascular necrosis eponymous conditiosn
Kienbock’s disease Lunate Perthe's: Hip Panner’s disease Capitellum of the humerus Freiberg’s disease Metatarsal head – usually the second Köhler’s disease Navicular
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Hilton's law
Hilton’s law, which states that a joint is supplied by the same nerves as the muscles that move the joint,
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Osteochondritis dissecans
Mostly commonly affects medial epicondyle of distal femur Osteochondral fragment becomes partially or totally separated If partial: rest and conservative managment Complete or mechanical symptoms: fixation or removal of loose bodies
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Osgood-Schlatter disease
Traction apophysitis of patellar tendon insertion Pain, tenderness and swelling at the tibial tubercle, exacerbated by exercise, are diagnostic Radiographs are unnecessary if bilateral, if unilateral ?maliganncy so imaging required Mx: relative rest and analgesia, and the condition resolves once the apophysis has fused
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Fibular hemilemi
Congenital failure of formation of the lateral ‘column’ of the lower leg
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Blount's disease
Disordered growth in the posteromedial proximal tibial physis Presents with porgressive and severe tibia vera + intoeing Surgical management necessary
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Congenital pseudoarthrosis of the tibia
Rare condition presents clinically with an anterolateral bow of the tibia with or without a fracture.
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Congenital pseudoarthrosis of the tibia
Rare condition presents clinically with an anterolateral bow of the tibia with or without a fracture 50% are associated with neurofibromatosis
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Paediatric knee and tibial conditons
Osteochondritis dissecans – better prognosis in children than adults Discoid meniscus – usually lateral, may require surgery Anterior knee pain – treatment almost always conservative Fibular hemimelia – associated with abnormalities from the foot proximally (foot worse than hip), the tibial bow has an anteromedial apex Blount’s disease – clinically, a sharp proximal tibial angulation Congenital pseudarthrosis of the tibia – the tibial bow has an anterolateral apex Posteromedial apex tibial bow – largely physiological, the bow improves with time but the limb may be short
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Congenital talipes equinovarus
Deformed in three planes -Hindfoot is in equinus and varus -Midfoot cavus and -Forefoot lies adducted and apparently supinated, although actually pronated relative to the hindfoot. M > F 50% bilateral Most cases are idiopathic but neuromuscular causes include spina bifida and arthrogryposis Scoring systems (Pirani/Dimeglio), are used to assess the severity
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Radial club hand
Associated with VACTERL syndrome -abnormal vertebrae, anus, cardiovascular system, trachea, oesophagus, renal system and limb buds - short radius -deformed ulna - +/- an absent thumb Mx: balance of conservative measures, including physiotherapy and splinting, and judicious surgery to centralise and stabilise the hand and wrist on the single bone forearm
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Radioulnar synostosis
Presents with a fixed forearm position in childhood
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Congenital radial head dislocation
Usually posterolateral vs traditional traumatic anterior
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Congenital toricollis
Usually caused by moulding but may present with fixed sternocleidomastoid contracture or with a palpable ‘tumour’ within the muscle. There is a strong correlation with DDH Most cases resolve with stretching Persistent cases develop facial asymmetry and require surgical release of the sternocleidomastoid at one or both ends.
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Kocher et al. Septic arthritis
Fever > 38.5 Non-weight bearing ESR >40 WCC >12 0: 2% 1: 9.5% 2: 35% 3: 72.8% 4: 93%
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Tibial metaphyseal corner injuries
= Non-accidental injury
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OSteomalacia
Issues with bone mineralisation low Ca low vit D low Phos, high ALP
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Osteoporosis
Issues with bone remodelling bloods all normal tx: Alendronic acid Bisphosphonates Raloxifene (SERM, + at bone and - at breast) Strontium Ranelate
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Which muscles make up the pes anserinus
sartorius, gracilis, and semitendinosus muscles
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Pes Anserinus bursitis
pain walking up and donw stairs over the proximal medial tibia
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Management of impacted humeral fracture
Impacted fractures of the surgical neck are usually managed with a collar and cuff for 3 weeks followed by physiotherapy.
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When is ORIF used in humeral fracture
Most commonly used. Plate and screw fixation. Can reconstruct complex fractures.
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When is IM Nail used in humeral fractures?
Suitable for extra-articular configuration, predominantly surgical neck +/- GT fractures.
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When is hemiarthroplasty used in humeral fractures?
Used for un-reconstructable fractures in the older patient who has good glenoid quality.
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When is total shoulder repacement used?
Unconstructable fractures where high functioning shoulder is required (hemiarthroplasty will cause glenoid erosion)
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What is the most common cause of shoulder pain?
Subacromial impingemenet
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Brown Sequard syndrome
Hemisection of the spinal cord Ipsilateral paralysis Ipsilateral loss of proprioception and fine discrimination Contralateral loss of pain and temperature