Extremity X-Ray Review
Extremity X-Ray Review
Avascular Necrosis
Avascular Necrosis: Adult
•Idiopathic, trauma, steroids, alcoholism, sickle
cell disease, Gaucher’ s disease, cassion
disease, radiation, SLE, and pancreatitis
•Most common location is femoral head
•Pain with weight bearing, decreased ROM
•Sclerosis, subchondral fracture (crescent sign),
flattening and bone deformity (step sign).
Secondary DJD may occur.
•Post traumatic AVN: Femoral head, lunate,
proximal scaphoid, body of talus
Avascular Necrosis: Adult
•SLE and sickle cell: Humeral head and
talus
•AVN vertebral body: Increased density
and collapse. Gas within vertebral body is
pathognomonic.
•MRI is the most sensitive modality
Legg-Calvé-Perthes Disease
• Males, between the ages of 3 and 12 years (peak age 4-
8). It is bilateral in approximately 10% of cases. Rare in
blacks
• The onset may be insidious or sudden. The patients
have pain, develop a limp and have limitation of motion
of the hip joint. The symptoms are worsened by activity
and relieved by rest. It is a self-limiting disease of 2-6
years in duration.
• Stage 1 is the avascular stage. The early x-ray findings
include: joint effusion with distention of the joint capsule.
The joint space may be widened (tear drop distance).
Lateral displacement of the head of the femur
(Waldenstrom’ s sign).
Legg-Calvé-Perthes Disease
• Stage 2 is the necrotic stage:
- The earliest osseous manifestation is a radiolucent line
(crescent or rim sign). This is an arc-like translucent
zone that develops in the subchondral bone close to the
articular surface.
- There will be an apparent increase in the density of the
epiphysis and is referred to as a “snow cap”appearance.
- Radiolucent areas develop within the femoral
epiphysis that represents areas of necrotic bone that are
undergoing lysis (demineralization). The
demineralization is due to an ingrowth of granulation
tissue.
-The epiphysis becomes irregular, fragmented and
flattens (collapses).
Legg-Calvé-Perthes Disease
•Stage 3 is the healing stage: Healing by
replacement of the dead tissue with new bone
takes from one to several years.
•Stage 4 is the end stage (hip deformity):
- There is usually flattening of the femoral
epiphysis (mushroom deformity) and a short,
broad femoral neck.
-Coxa plana, coxa magna, and coxa valga.
- There may be enlargement of the acetabulum
to accommodate the abnormal femoral head.
- The development of degenerative changes
early in adult life is common.
Acute Irritable Hip Syndrome
(Transient synovitis of the hip, observation hip,
irritable hip)
•The most common diagnosis of hip pain during
childhood
•Acute onset of pain in the hip, groin, or knee
combined with a limp and limitation of motion in
a child of about 3 years of age. With rest and
conservative care, the clinical symptoms
generally resolve in a week or two.
•The differential diagnosis would include: Legg-
Calvé-Perthes disease, infection, inflammatory
arthritis
Osteochondritis
(Osteochondrosis) Disscans
•Fragmentation and possible separation of
a portion of the articular surface
•The age of onset varies from childhood to
middle age, but an onset in adolescence is
most frequent
•Males > females
•The most common location is the lateral
portion of the medial femoral condyle
Spontaneous Osteonecrosis of
Knee (SONK)
1. Multiple myeloma
2. Osteosarcoma
3. Chondrosarcoma
Most Common Malignancy
of Bone
•Metastatic carcinoma
Round Cell Tumors
•Ewing’s sarcoma
•MM
•Non-Hodgkin’ s lymphoma (reticulum cell
sarcoma)
Osteoma
•Arising in membranous bones: sinuses
(frontal most common), skull and mandible
•Dense sclerotic mass
•Gardner’ s syndrome: intestinal polyposis,
osteomas, fibromas of the soft tissue, and
sebaceous cysts of the skin
Osteoid Osteoma
• Night pain, relieved by aspirin
• Pain, tenderness, increased skin temperature over area.
Pain with motion, convex scoliosis away from the
involved site (painful scoliosis in children), torticollis-
cervical spine
• 10-25 years of age. 2:1 males
• About 50% of the cases involve the femur and tibia
• 10% are spinal: Lumbar (59%) and cervical (27%).
Lamina, articular process and pedicle.
• Radiolucent nidus surrounded by extensive reactive
sclerosis. The nidus is usually less than 1cm in diameter
(<2cm)
Osteoblastoma
(Giant Osteoid Osteoma)
•2:1 male, below 30 years of age
•Involve spine (SP, TP, neural arch), long
bones (femur and tibia) and small bones of
hands and feet
•X-ray: Radiolucent expansile lesion with
calcification. Usually 2cm or larger
Osteogenic Sarcoma
(Osteosarcoma)
•10-25 years of age
•Distal femur 44%, proximal tibia 17$, and
proximal humerus 15%.
•X-ray: metaphysis, bone destruction,
calcific neoplastic tissue, periosteal new
bone formation (spiculated and Codman
triangles). 50% are sclerotic, 25% mixed.
Enchondroma (Chondroma)
•Most common benign tumor of the hand
•50% occur in the hands and feet
•Femur, humerus and ribs. 10-30 years of
age, 1:1
•X-ray: radiolucent lesion with sharp,
sclerotic margins (scalloped). Punctate or
stippled calcifications
Multiple Enchondromatosis
(Ollier’
s Disease)
•Autosomal-dominant disorder
•Most are broad-based. Lumps around
joints. Diaphyseal aclasis.
•Malignant transformation 5-25%
Chondroblastoma
(Codman’ s Tumor)
•Arises in epiphysis or apophysis
•Teenagers (10-20 years of age) 2:1 males
•Pain and swelling
•Round or oval lytic lesion with stippled or
fluffy calcifications (“
fluffy, cotton wool”
appearance)
•Proximal humerus (tuberosities), proximal
femur (trochanters), distal femur, proximal
tibia
Chondrosarcoma
•30-60 years of age
•Pelvis, femur, shoulder girdle, ribs, and
sternum
•Most common malignant tumor of scapula
and sternum
•Bone destruction with scattered
calcifications (popcorn, stippled, or
snowflake)
Non-ossifying (Non-Osteogenic)
Fibrous (Xanthoma, Fibroxanthoma)
Fibrous Cortical Defect
•FCD
- small intracortical lesion less than 2cm
- 30-40% of all children have, 4-8 years of age
- Distal femur, most common site
•NOF
- larger lesion (> 2cm), possible path fracture
- Metaphyseal: distal femur, proximal tibia, distal
tibia, and distal fibula
- Elongated lucent lesion with well-defined
sclerotic border, thin cortex, scalloped margins
Ewing’
s Sarcoma
•80% under 30 years of age
•Pain and swelling. About one-third have fever,
anemia, leukocytosis, and increased ESR
(simulating infection)
•Before age 20, involves the shaft (diaphysis) of
long bones (femur, tibia, fibula, and humerus)
•After age 20, involves pelvic bones
•X-ray: Diaphyseal, permeative bone destruction,
soft tissue mass, periosteal reaction (laminated,
onion skin)
Giant-cell Tumor
(Osteoclastoma)
•80% occur in patients older than 20 years
(median age of 30)
•15% are malignant
•Distal femur, proximal tibia, distal radius,
proximal femur, sacrum, spine (vertebral body)
•50% involve distal femur and proximal tibia
•X-ray: geographic expanding radiolucent lesion
involving end of long bone (subarticular
extension). May have soap-bubble appearance.
Simple Bone Cyst (Unicameral
Bone Cyst, Solitary Bone Cyst)
•Fluid –containing cyst. 80-90% under 20 years
of age. 3-14 years of age, males 2:1
•Proximal humerus (50%), proximal femur (20%),
tibia and calcaneus
•X-ray: truncated radiolucency
- Active cyst: abuts the epiphyseal plate
- Latent cyst: is distal to the epiphyseal plate
- Fallen fragment sign or hinged fragment sign
Aneurysmal Bone Cyst
•Highly vascular expansive lesion containing a
cavity or cavities filled with bloody fluid
•80% occur below age 20
•Metaphysis of long bones: femur, tibia,
humerus, fibula, radius
•18% involve the spine (posterior elements)
•Very expansile, eccentric, lytic, metaphyseal
lesion (“blown-out”appearance
•Most common benign tumor of the clavicle
Chordoma
•Hand
- DIP joints: Heberden’ s nodes
- PIP joints: Bouchard’ s nodes
•Elbow: post-traumatic
•Shoulder: post-traumatic
•AC joint: common
•SI joint: mid to upper third of joint
Rheumatoid Arthritis (RA)
•Arthritis of unknown etiology that causes
synovial inflammation and articular destruction-
polyarticular
•The incidence is about 1% in the general
population. 3:1 females. Peak onset is between
the ages of 20-45 years.
•Lab: RF may be negative early, but eventually
becomes positive in 90% to 95% of cases. ESR
elevated and tends to parallel disease activity.
Rheumatoid Arthritis
•Hand:
- Early erosions at MCP (radial side of MC
heads) and PIP joints.
- MCP: ulnar deviation and volar subluxation
- Swan-neck: PIP hyperextension and DIP
hyperflexion
- Boutonniere: PIP hyperflexion and DIP
hyperextension
- Hitchhikers thumb: MCP flexion and IP
extension.
Rheumatoid Arthritis
•Wrist:
- Early erosions at distal radioulnar joint,
ulnar styloid, radial styloid, waist of
scaphoid, triquetrum, and pisiform
- Deformities: ulnar translocation, radial
deviation of hand, scapholunate
dissociation, dorsi- and palmar flexion
carpal instability patterns, and distal
radioulnar dissociation.
Rheumatoid Arthritis
•Elbow:
- Positive fat-pad sign, erosions of the distal
humerus, radial head, and coronoid
•Shoulder:
- Lysis of the distal clavicle, marginal humeral
head erosion
- Later: signs of rotator cuff tear –humeral head
elevation, concavity on the under surface of the
acromion, mechanical erosion of the medial
surgical neck of the humerus
Rheumatoid Arthritis
•Feet:
- MTP erosions (especially on the medial
side of the MT heads)
- Deformities: lateral deviation at MTP’
s,
hammer toes (flexion of PTPs or DTPs)
and cock-up deformities Hyperextended
MTPs)
- Calcaneal spurs
Rheumatoid Arthritis
•Knee:
- Suprapatellar effusions and popliteal
synovial cysts (Baker’ s cysts). All 3
compartments demonstrate symmetric
cartilage loss, erosion, and subchondral
cysts. Valgus deformity. Distal femoral
erosion –anterior mechanical erosion from
patella pressure.
Gout
•Asymmetric polyarthritis caused by deposition of
monosodium urate crystals in articular cartilage,
synovium, subchondral bone, and periarticular
tissues
•Acute gout most commonly affects the lower
extremity joints, especially the first
metatarsophalangeal joint (70%), with
excruciating pain and swelling
•Middle-ages or elderly males, women after
menopause
•Warm, tender, swollen, erythematous joint
Gout
•First MTP joint (podagra)
•X-ray
- Asymmetric, nodular deposits of calcium
urate (tophi) in periarticular tissues
- Intraarticular and periarticular erosions
show sclerotic margins and often have
elevated “ overhanging edges”extending
over tophaceous nodules
Calcium Pyrophosphate Dihydrate
Crystal Deposition Disease (CPPD)
•Pseudogout: clinical presentation with acute,
self-limited attacks of pain and swelling
mimicking gout
•Middle ages or elderly male
•Knee, wrist, second and third MCP joints
•X-ray
- Chondrocalcinosis: calcification of hyaline or
fibrocartilage. Most commonly involves
fibrocartilage.
•Synovial and capsular calcification are common
Chondrocalcinosis
•Calcification of hyaline or fibrocartilage
•CPPD, DJD, trauma, gout,
hyperparathyroidism, hemochromatosis,
Wilson’ s disease, ochronosis
Extremity Trauma
Stress Fractures
(Fatigue or March Fractures)
•Result from repeated application of abnormal
stress on normal bone
•Normally, bone remodeling occurs in response
to applied stress and consists of bone resorption
followed by new bone formation. If the applied
stress is increased or is continuous during the
period in which bone resorption predominates, a
stress fracture may occur. Increased
osteoclastic activity, microinfractions of bone,
and finally frank fracture.
Stress Fractures
• Bone scanning is useful to detect early stress
fractures. The bone will demonstrate increased
nuclide activity at the fracture site in 80% of
patients within 24 hours and in 95% of patients
within 72 hours.
• Characteristics of activities resulting in stress
fractures:
1. Activity is strenuous
2. Activity is often new or different
3. Activity is repeated with frequency
Stress Fractures
•Most common in the lower extremity:
metatarsal>calcaneus>tibia
•X-Ray
- Cancellous bone: thin zone of sclerosis
- Cortical bone: thin cortical lucency
followed by localized periosteal reaction
Acetabular Dysplasia
•Shallow, poorly developed acetabulum
Congenital Dysplasia of Hip (CDH)
Developmental Dysplasia of Hip (DOH),
Congenital Hip Dislocation (CHD)
•M:F = 1:8
•Females (2/3 - first born), infants born in breech
position (6:1)
•Putti’
s Triad
1. Delay in ossification of the capital femoral
epiphysis
2. Acetabular angle greater than 30 degrees
3. Proximal medial margin of the femoral
metaphysis is displaced lateral to Perkin’ s line
Pathologic Fractures
•A fracture involving bone in which the normal
integrity and strength are compromised
•Osteoporosis (most common cause),
osteomalacia, renal osteodystrophy,
hyperparathyroidism
•Benign lesions
•Malignant lesions
- Metastatic disease (second most common
cause)
•The proximal femur is involved in over 50% of
long bone pathologic fractures
Insufficiency Fractures
• Fractures that occur when normal or physiological stress
is applied to abnormally weakened bones
- Osteoporosis
- RA
- Osteomalacia/rickets
- Paget’ s disease
- Hyperparathyroidism
- Renal osteodystrophy
- Radiation therapy
- Steroid-induced osteopenia
• Location
- lower extremity (femoral neck), sacrum, ilium, pubic
bone
Birth Fractures
•Clavicle fractures most common
•The humerus is the most frequently
fracture long bone
•Clavicle, proximal humerus, proximal
femur and distal humerus
Slipped Femoral Capital Epiphysis
(SFCE) (Epiphysiolysis)
•13-14 years in boys, 11-12 years in girls,
greater incidence in boys, overweight
(Fröhlich’s syndrome)
•Boys 2:1 left side, girls 1:1 right vs left
side, 20-30% bilateral
•The proximal femoral epiphyseal plate is
the only epiphyseal plate that is subject
normally to shearing stress
•Salter-Harris Type 1 epiphyseal injury
X-Ray of SFCE
•Do frog-leg view
•The head is displace posteriorly, downward and
medially
•Limp, leg externally rotated, decreased ROM
(limited internal rotation), synovitis
•Often complain of knee pain or pain in the
anterior thigh and do not associate their problem
with the hip
•Deformity, osteoarthritis, avascular necrosis,
chondrolysis
Epiphyseal Injuries
•80% of epiphyseal injuries occur between age
10 and 16 years. Distal humerus usually occur
prior to the age of 10.
•Most common sites:
1. distal radius
2. distal tibia
3. phalanges
•In children, ligaments are functionally stronger
than bone (sprains in adults, fractures in
children)
•Failure is usually from torsion and not tension at
the physis
Salter-Harris Classification
•I - 6% transverse fracture through physis
•II - 75% fracture throughout physis with
metaphyseal fragment
•III - 8% fracture through physis and
epiphysis
•IV - 10% fracture through epiphysis,
physis, and metaphysis
•V - 1% crush injury of physis
Epiphyseal Injuries
• Type II
- distal radius is most common site (up to 50%)
- distal tibia, distal fibula, distal femur, and ulna
- the metaphyseal fragment = Thurston-Holland fragment
• Type III
- distal tibia is most common site
• Type IV
- under 10 years of age –lateral condyle of humerus
- over 10 years of age –distal tibia
• Tibia V
- distal femur (most common location)
- proximal and distal tibia
Complications of
Epiphyseal Injuries
•Complete growth arrest
•Progressive limb length inequalities (short
or long)
•Progressive angular deformities
•Other unusual joint deformities due to
avascular necrosis
Pelvis –Avulsion Fractures
•ASIS –sartorius
•AAIS –rectus femoris
•Ischial tuberosity –hamstrings
Pelvic Fractures
•Fractures involving the ischial and pubic
rami are the most common fractures of the
pelvis
Sacral Fractures
•Horizontal
•Vertical
Acetabular Fractures
•Posterior rim
•Posterior column
•Central (most common)
- Bursting: central fracture with dislocation
•Anterior column
Hip Dislocation
•Posterior ( most common)
•Anterior
•Central fracture - dislocation
Hip Fracture
•Hip fractures in the elderly can be very
difficult to detect. A negative plain film in
an elderly patient with hip pain following
trauma does not exclude a femoral neck
fracture. MRI imaging is very useful to
demonstrate fractures that are occult.
Proximal Femur Fractures
•Subcapital
•Midcervical (transcervical)
•Basic cervical (base of neck)
•Intertrochanteric
•Subtrochanteric
•Greater trochanteric
Complications of Proximal
Femur Fractures
•Nonunion
•Avascular necrosis
Maisonneuve Fracture
•Intercondylar (T.V.Y.)
•Condylar
•Supracondylar
Proximal Tibia
•Depression fracture or tibial plateau
•Fractures of the lateral plateau are more
common (valgus stress)
•Oblique views may be necessary to
diagnose
•Often seen in auto-pedestrian accidents
where the plateau was at the height of
fenders and bumpers (bumper fracture)
Segond Fracture
•Cortical avulsion fracture of proximal
lateral tibia immediately distal to lateral
plateau
•External rotation and varus stress (lateral
capsular ligament)
•Associated with ACL tear (75-100%) and
meniscal tear (67%)
Pelligrini-Stieda Calcification
•Fracture-dislocation of tarsometatarsal
joints.
Shoulder Dislocation
•Anterior 97%
•Posterior 2%
•Superior 1%
Anterior Dislocation of Shoulder
•Subcoracoid
•Subglenoid
•Subclavicular
•Intrathoracic
•Luxatio erecta
•Superior
Posterior Dislocation of
Shoulder
•Traumatic
•Electric shock
•Seizures (Epileptic convulsion)
•Shock therapy
Complications of
Shoulder Trauma
•Adhesive capsulitis
•Rotator cuff tear
•Associated fractures
- greater tubercle with anterior dislocation
(flap fracture)
- lesser tubercle with posterior dislocation
- Bankart lesions (fracture of inferior
glenoid labrum)
Complications of
Shoulder Trauma
•The glenoid rim is fractured in 20% of patients
with fracture/dislocation of the shoulder
•Hill-Sachs deformity (Hatchet defect): A
compression fracture on the posterolateral
aspect of the humeral head caused by impaction
against the anterior rim of the glenoid fossa.
- See in 27% of acute anterior dislocations and
74% of recurrent anterior dislocations.
Fractures of the
Proximal Humerus
•80% have no significant displacement
because fragments are held together by
the rotator cuff, the joint capsule, and the
intact periosteum
•Surgical neck fracture
•Greater tubercle (flap fracture)
Pseudodislocation of Shoulder
(Hanging, Drooping, Inferior
Subluxation of the Humeral Head)