Académique Documents
Professionnel Documents
Culture Documents
PA 532
Synovial Fluid Analysis
Joint (arthrocentesis) or bursa
Indications: r/o infection in acute joint pain with
effusion and severe acute pain with joint ROM
Cell count
Crystals
Gout: (+) negatively birefringent, needle-shaped crystals
Pseudogout: (+)positively birefringent, rectangular-shaped
crystals
Culture, +/- sensitivity
Contraindications: Arthroplasty!
Measure Normal Non-Inflammatory Inflammatory Purulent
Volume (mL) <3.5 Often >3.5 Often >3.5 Often > 3.5
T1 T2
Radiographic Findings Of Selected
Orthopedic Conditions
How to Order Xrays:
Always order at
least 2 views!
Weightbearing
films for OA
Normal OA
RA
OA vs RA Radiographically
OA RA
Degenerative/wear and Proximal joints of hands
tear and wrists
CMC, MCP, PIP
Hips, knees, hands
Bilateral and symmetrical
Subchondral sclerosis
Joint erosion
Subchondral cysts Joint space narrowing
Joint space narrowing Eventual fusion
Osteophytes Early: soft tissue swelling
and osteoporosis
Late: ulnar deviation at
MCP joints, subluxation of
MCP joints
Avascular Necrosis
AVN:
- Bone death leading to
collapse of the
affected bone
- Usually involves bone
with inherent poor
blood flow:
scaphoid, talus,
femoral head, etc
Osteochondritis Dessicans
Septic Arthritis
Destruction of:
Articular cartilage
Long, contiguous
segments of
adjacent articular
cortex
Rapid
Charcot
Osteomyelitis
Degenerative
Ankylosing Spondylitis
Bamboo Spine
Burst Fracture
Jefferson Fracture
Hangmans Fracture
Clay-Shovelers Fracture
Degenerative Disc Disease
Herniated vs Bulging Discs
Scoliosis
Femoral Neck Stress Fracture
Femoral Neck Stress Fracture
Femoral Neck Stress Fracture
Lisfranc Fracture
Jones Fracture
Jones Fracture & Avulsion Fracture
5th Metatarsal Base Fracture
Weber A Fibula Fracture
Weber B Fibula Fracture
Weber C Fibula Fracture
Bimalleolar Fracture
The rest of the story
Maissoneuve Fracture
Pes Cavus & Pes Planus
Hallux Valgus
Patellar Tendon Rupture: Patella Alta
Tibial Plateau Fracture
? Fracture
? Fracture
Smith & Colles
? Fracture
? Fracture
Snuff Box Tenderness
Smooth &
well rounded
FYI
Medpix
Wheelessonline.com
Rheumatology Diagnostic Studies
PA 532
Antibodies
Immunoglobulins on surface of B lymphocytes
IgG, IgM, IgE, IgA, IgD
Produced in response to a foreign protein or
substance within the body or randomly
Autoantibodies
Antibodies manufactured by the immune
system directed against one or more of the
individual's own proteins
Usually a component of a cell
i.e. mitochondria, nucleus, centromere, ribonuclear
protein, histones, core proteins, DNA
Autoantibodies
Indirect immunofluorescence assays identify
autoantibodies reactive with antigens in
particular tissues or subcellular compartments
(e.g., nuclear antigens)
Fixed tissue samples/cells are overlaid with
patient sera and then washed.
Detect autoantibodies that are bound to sample
with fluorescein-labeled antiserum to Ig
Autoantibodies
Directed to:
Nuclear material antinuclear antibodies
(ANA)
Cytoplasmic material anticytoplasmic
antibodies
Membrane
Mixed Connective Tissue Disorders
Patients with overlapping s/s with
rheumatologic disorders, ex:
SLE, scleroderma, inflammatory myopathy
SLE w/ Raynaud, polyarthritis, myositis,
pulmonary HTN
RA & SLE or SLE & scleroderma
Can also be hereditary
Osteogenesis imperfecta, Ehlers-Danlos
Syndrome, Marfan Syndrome
Common ANA and Autoimmune
Disease
ANA Screen Autoimmune Disease
Anti-Extractable Nuclear Antigen (ENA) SLE, MCTD
- Anti-ribonucleoprotein (RNP) MCTD, SLE, PSS
- Anti-sm or Anti-Smith SLE
- Anti-Jo-1(antihistidyl transfer synthase) Polymyositis, dermatomyositis
- Anti-SS-A (anti-Ro) and anti-SS-B (anti- Sjorgren syndrome, SLE (ANA negative)
LA)
- Anti-scleroderma- 70 PSS
Anti-native double-stranded DNA (dsDNA) SLE
Anti-single-stranded DNA (ssDNA) SLE
Anti-centromere PSS, SLE
Anticytoplasmic Antibodies Diseases
Antimitochondrial antibodies (AMA) Primary Biliary Cirrhosis
Antineutrophil Cytoplasmic Antibody Granulomatosis with Polyangitis, Churg-
(ANCA, C-ANCA, P-ANCA) Strauss Syndrome, CF
P-ANCA: Ulcerative colitis, PSC
Antimiscrosomal
-Antithyroid Hashimoto thyroiditis
- Anti Liver Kidney Microsomal Autoimmune hepatitis (Anti-LKM-1)
Antibody (Anti-LKM)
Antithyroid Antibodies Hashimotos thyroiditis, Graves disease,
- Antithyroglobulin lymphocytic thyroiditis in children
- Antithyroid peroxidase antibody (Anti-
TPO)
Antiribosomal SLE
Anti-RNA Scleroderma
Anti-cardioplin antibodies (ACA) SLE (with high risk for antiphospholipid
antibody syndrome)
Anti smooth muscle antibody (A-SMA, aka Autoimmune hepatitis, PSC
Antiactin antibody)
Cell Membrane Antibodies
Cell Membrane Antibodies Disease
Antiglomerular Basement Membrane Goodpasture syndrome (autoimmune-
Antibody induced nephritis)
Antinuclear Antibody (ANA)
The most commonly performed screening test in
patients suspected of connective tissue disease
Serologic hallmarks for systemic or organ-specific
autoimmune disease
Most common circulating autoantibody in many
autoimmune diseases (SLE, autoimmune hepatitis)
Results given as a titer and type of
immunofluorescence pattern
ANA titer is positive if 1:80 or greater
Pattern: homogeneous, outline/rim, speckled, nucleolar
ANA Patterns & Associations
In general,
there is a
poor
correlation
between the
pattern &
underlying
disease
ANA
Most sensitive laboratory test for SLE
Best single test to rule out SLE*
ANA is first line screen
95% sensitive, 49% specific
(+) ANA for SLE is usually titer of 1:160
SLE is a disease of overproduction of
autoantibodies to nuclear antigens
SLE
(+) ANA SLE
Other antibody studies must be done to confirm
dx and/or consideration of clinical symptoms
Other autoantibodies highly specific for SLE:
dsDNA (75% sensitive)
Anti-SM (25% sensitive)
What if ANA is (-) and SLE is suspected?
ANA negative SLEAnti-SSA
Anti-DNA Antibody
Indications: diagnosis and follow-up of SLE
High titers are characteristic of SLE
> 200 IU/ml
Low-intermediate titers
chronic hepatitis, infectious mono, biliary cirrhosis,
other autoimmune/rheumatic disorders
Titer decreases with treatment of SLE
Titer increased with SLE exacerbations or onset
of GN
Anti-DNA Antibody
Two types:
Anti-dsDNA: commonly found
Anti-ssDNA: less sensitive, less specific for SLE
These complexes induce the complement
system leading to local or systemic tissue
damage!
Anticardiolipin Antibody
Some patients with SLE have this antibody
which puts them at risk for anti-phospholipid
syndrome
Anti-phospholipid syndrome antibodies include
anticardiolipin ab (40% SLE patients)
lupus anti-coagulant (50% SLE patients)
which prolongs PTT however not assoc w/ incr bleeding!
SLE pt w/Anticardiolipin ab + lupus anticoagulant =
risk for anti-phospholipid syndrome
Anticardiolipin Antibody
Indications:
Venous and arterial thrombosis, neuropsychiatric
disorders, recurrent spontaneous abortion, and
thrombocytopenia
May also be found in drug induced lupus, acute
infection, and elderly persons, IgA, IgG, IgM
Anti-Centromere Antibody
Subtype of antinuclear antibodies (ANA)
Used to support the diagnosis of CREST
syndrome
(+) in 90% CREST (limited disease scleroderma)
Anti-ENA
Extractable Nuclear Antigens (ENA)
Consist of RNA and protein
Type of ANA
Useful in assisting diagnosis of SLE or mixed
connective tissue disease
Helps r/o other rheumatologic diseases
Anti-ENA
Types of Anti-ENA
Anti-Smith (SM) antibody*
30% SLE
8% MCTD
Absent in other rheumatoid-collagen diseases
Anti-RNP (ribonucleoprotein) antibody*
100% MCTD
25% of SLE, discoid lupus and scleroderma
Anti-Jo-1 antibody
Autoimmune interstitial pulmonary fibrosis, polymyositis,
dermatomyositis
Anti-SSA & Anti-SSB used to dx Sjogren
Antiglomerular Basement Membrane
Antibody
Detects presence of circulating GBM ab found
in autoimmune GN or lupus nephritis
Sample can be blood (circulating) or tissue
biopsy
Circulating blood is quicker and less invasive
Anti-SSA/SSB/SSC Antibody
Indications: Suspected Sjogren Syndrome (SS)
SSA(+): 60-70% pts w/ Sjogren
SSB(+): 50-60% pts w/ Sjogren
SSA (+) + SSB(+) = Sjogren diagnosis
SSC (+): 75% pts w/RA or RA assoc. Sjogren
SSA & SSB almost never found in RA assoc. Sjogren
Anti-SSA/SSB/SSC Antibody
Indications: SLE
SSA (+) in 25% of pts w/ SLE
Most patients with ANA-negative SLE will
have (+)SSA
Anti-SCL-70
Indications: Suspected scleroderma
(+) in 45% of patients with scleroderma
Does not differentiate limited vs diffuse
scleroderma
Also seen in
SLE, MCTD, Sjogren, Polymyositis, Rheumatoid
Arthritis
Anti-mitochondrial (AMA)
Anti-cytoplasmic antibody directed against a
lipoprotein in the mitochondrial membrane
Useful in diagnosis of:
Primary biliary cirrhosis (+ in 94%)
Cholestasis, chronic and acute hepatitis,
extrahepatic obstruction
Also (+) in patients with autoimmune hepatitis
from SLE, scleroderma*
Antineutrophil Cytoplasmic Antibody
(ANCA)
Indications: Suspected Granulomatosis w/
Polyangiitis
Two patterns
Cytoplasmic (C-ANCA)
Perinuclear (P-ANCA)
Increased levels in many diseases, but commonly
associated with granulomatosis with polyangiitis
P-ANCA is associated with ulcerative colitis and
primary sclerosing cholangitis
Anti-Smooth-Muscle-Antibody
Anticytoplasmic antibody
A.K.A. anti-actin antibody
(+) in patients with autoimmune hepatitis
HLA-B27
Human Lymphocyte antigen B-27
Normally occurs: 8-10% Whites, 2% African
Americans
Higher occurrence in some Native American &
Eskimo
Indications: Support diagnosis of certain
diseases (AS, reactive arthritis)
Also helpful in paternity testing as well as
checking histocompatibility in a tissue transplant
HLA-B27
Positive in:
90% AS patients
75% Reactive arthritis patients
50% Psoriatic and inflammatory bowel disease
patients who also have sacroiliitis
Example of genes + environment
Risk of developing reactive arthritis is
0.2% general population
2% in HLA-B27 patients
20% in HLA-B27 pts infected with Salmonella, Shigella or
enteric organisms
Rheumatoid Factor (RF)
Indications: Suspected RA or rheumatologic
disease
The titer is positive if > 1:80
Positive in 80% of patients with RA
Sensitivity of 66.3%, Specificity of 82.1%
Titers <1:80
SLE, scleroderma, Sjogren syndrome, other
rheumatologic diseases
Does not disappear with decreasing sx
Negative does not rule out RA
Anti-CCP Antibody
Anticyclic-citrullinated peptide antibody
Indications: Unexplained joint inflammation
Especially if after (-) RF with suspicion for RA
Sensitivity 67.5%, Specificity 99.3% for RA
This test has a higher specificity than RF for RA
Anti-CCP Antibody
Anti-cyclic-citrullinated-peptide
Specific for rheumatoid arthritis, early in
course of disease
Which is important for treatment
Marker for disease progression
CRP
Indications: Inflammatory illness
C- reactive protein
Protein made by the liver in response to inflammation
More sensitive (& faster) than ESR
For rheumatologic disorders this is used to
screen, or build a case for a diagnosis
Also used to detect bacterial infections, tissue
infarct (MI), risk of cardiovascular ischemic
events, etc.
Erythrocyte Sedimentation Rate (ESR)
Indications:
detection of acute or chronic inflammation,
infection, neoplasm, and tissue necrosis/infarction
Nonspecific
Vague symptoms or differentiation
Monitor therapy and progression
Autoimmune Disease & Positive
Autoantibodies
SLE ANA, ds DNA, ss DNA, anti-SSA,
anti-cardioplin (ACA)
Sjogrens ANA, anti SSA, anti SSB
Scleroderma/CREST ANA, anti-Scl-70
Anti-centromere
MCTD ANA, anti-RNP, RF, ss DNA
Autoimmune Hepatitis ANA, Anti-LKM
PA 532
Head Imaging Modalities
CONVEX CONCAVE
Epidural Hematoma
Note the midline shift
and loss of normal
tissue contrast. Call
the neurosurgeon!
On your
differential
diagnosis for
subacute
confusion in
an older adult
R L
Subarachnoid Hemorrhage
Normal NPH
MRI
Neurology Diagnostics II
PA 532
Brain Tumors
Contrast MRI
MS
MRI
Is
Study
Of
Choice
23 year-old female with progressive
weakness and visual disturbances
EEG
EEG
Important in diagnosing epilepsy, however
cannot be used alone to make the diagnosis.
Limitations
EEG patterns can be caused by a variety of different
neurologic diseases
Not all cases of brain disease are associated with EEG
abnormalities
Many disease cause more than one EEG pattern
Intermittent EEG changes may not appear
EEG can be abnormal in persons without disease
EEG Results
Evaluating Seizure in Adults
MRI to rule out brain lesion
Labs
R/O Metabolic or toxic cause (CMP, toxicology screen)
Serum Prolactin level - may rise shortly after generalized
tonic-clonic seizures and some partial seizures if 10-20
minutes after an event and compared to baseline 6 hours
later.
Lumbar puncture if infection is suspected
If a space occupying lesion is suspected (causing focal
neurologic deficit, seizure or papilledema) a CT should be
done BEFORE the LP d/t risk of brain herniation
A normal EEG does not rule out epilepsy
Nerve Conduction Studies
Focal and generalized disorders of peripheral
nerves
Aid in the differentiation of primary nerve and
muscle disorders
Classify peripheral nerve conduction
abnormalities due to:
Axonal degeneration, demyelination and
conduction block
Follow up to determine prognosis
Nerve Conduction Study
Electromyography (EMG)
Clinical study of the electrical activity of
muscle fibers individually and collectively
Lumbar Puncture
LP: Indications
Urgent
Suspected CNS infections (meningitis)
Suspected subarachnoid hemorrhage (SAH) in
patients with a negative CT scan
Nonurgent
Pseudotumor cerebri
NPH
CNS syphilis
MS
LP: Contraindications
Increased intracranial pressure
Patients with altered level of consciousness, focal
neurologic deficit, new-onset seizure, papilledema
or immunocompromised
Imaging needs to be done first to decrease risk of brain
herniation
Thrombocytopenia or bleeding disorders
Risk of post-LP subdural/epidural hematoma
Order Platelet count, INR, PTT
Platelet count <20,000/uL LP is contraindicated
(protocols vary by institution)
Suspected spinal epidural abscess
Potential Complications
Post-LP headache* (10-30% of patients)
Infection
Bleeding
Radicular pain or numbness, back pain (may need to
image first)
Cerebral herniation*
CT first r/o elevated ICP, mass (last slide)
Unless bacterial meningitis is suspected do LP first
unless:
Symptoms (last slide) of increased ICP, in pt with suspected
meningitis, then give ABX prior to imaging
Normal Composition
Pressure: 50-180 mmH20
RBC: None
WBC: Lymphs 60-70%, Monocytes 30-50%,
Neutrophils none
C & S: No growth
Protein: 15-50 mg/dL
Glucose: 40-70 mg/dL
Lactate 10-20 md/dL
Normals: Protein: 15-50 mg/DL; Glucose: 40-70 mg/dL
PET Scan
Positron Emission Tomography
Used for evaluation of the brain anatomy &
physiology
Radioactive chemicals are given IV then detected
during CT scan to demonstrate metabolic process
of cells/blood flow (physiology)
Brain PET most commonly uses radioactive
fluorine (FDG)
PET Scan
Increased activity:
Epilepsy, Parkinson disease, Huntington
disease.
Decreased activity:
Alzheimer disease, brain
trauma/hemorrhage.
Now, you try
Q: Where is the
bleeding?
Classic Triad: gait
disturbance,
urinary
incontinence, and
dementia
Radiology for PA
Students
Part IV: Orthopedic
Imaging
kgraham@uwlax.edu
Objectives
Determine the most appropriate imaging study
to order for a particular musculoskeletal or
neurological complaint
Use appropriate terminology to describe
fractures, subluxations, and dislocations
Recognize common adult and pediatric fractures
Describe the radiographic features of OA, RA,
and osteomyelitis
Identify normal anatomy on C-spine radiographs
Determine when imaging for back pain is
appropriate
NOTE: The objective of this
lecture is not to review
normal skeletal anatomy.
You should be able to identify
normal skeletal anatomy on
conventional radiographs
based on your recent
anatomy course. Normal
bone anatomy can be
reviewed in your radiology
and anatomy texts.
Skeletal Imaging
Conventional radiographs are first line for
evaluating most injuries and arthritis
CT
Bone detail: extent and severity of fracture
Fracture fragment evaluation
MRI
Occult fracture evaluation
Tumor evaluation
Soft tissue injuries ligaments, meniscus tears,
rotator cuff problems, etc.
3D Reformatted CT
Skeletal Imaging
Bone Scan
Also called bone scintigraphy
Involves the IV injection of a radioactive tracer that
accumulates in bone that is undergoing rapid turnover
or growth
Has been replaced by MRI for many indications
Still used to screen for stress fractures, osteomyelitis,
and skeletal metastases
Ultrasound
Newer applications include evaluating superficial
structures (tendons, muscles, soft tissue masses) and
guiding injections
Bone Scans
Patient with
metastases of
breast carcinoma to
the spine and pelvis
Skin is
penetrated
This is an open tib-fib fx.
Note that the fractured
bone breaks the soft
tissue plane.
Fracture Terminology:
Comminuted (complex) fracture
Comminuted
forearm
fracture
Figure 22-7
Fracture Terminology:
Fracture line descriptions
Figure 22-7
Fracture Terminology:
Fracture line descriptions
A spiral fx
in a child
who is not
walking is
suspicious
for child
abuse
Figure 22-7
Fracture Terminology:
Angulation
A: A medially
displaced
transverse
midshaft fracture of
the humerus
Fracture Terminology:
Distraction & Overriding
This drawing
depicts an
impacted femoral
neck fx
Fracture Terminology:
Stress Fracture
Note that stress
fractures are opaque
Summation of rather than lucent
microfractures caused
by unusual or excess
stress; frequently seen
in athletes
The tibia is a
common site of
stress fx in all age
groups
Fracture Terminology:
Pathologic Fracture
Fracture through a bone
abnormality, benign or
malignant; can occur
with minimal or no
trauma
Figure 21-27
Fracture Terminology:
Avulsion Fracture
Fracture of a bony fragment that is produced by
the pull of a ligamentous or tendinous attachment
This is an
avulsion fx
of the middle
phalanx
Fracture Terminology:
Avulsion Fracture
This is an
avulsion fx
of the knee
due to an
ACL tear
Pediatric Fractures:
Normal physis
Metaphysis
Physis (growth
plate) bone
formation occurs on
both sides; this is
the weakest part of
a growing bone
Epiphysis
Type I = S = Separated
Type II = A = Above epiphysis
Type III = L = Lower (epiphysis)
Type IV = T = Through
Type V = R = Rammed
Pediatric Fractures:
Salter-Harris Fractures
Type III
Type II
Figures 22-15, 16
Pediatric Fractures:
Salter-Harris Fractures Type IV
Type V
Figures 22-17,18
Pediatric Fractures:
Greenstick Fracture
Order a
scaphoid
view
Common Fractures:
Scaphoid Fracture
5% of scaphoid
fractures have
complications
Nonunion
Osteoarthritis
Avascular necrosis
Common Fractures:
Scaphoid Fracture
This scaphoid fx is
easily seen; but if you
do not see a fx initially, White arrow
order MRI or immobilize identifies an
ulnar
and obtain f/u films styloid
fracture
Always refer these to
ortho this one was
surgically repaired
Common Fractures:
Fracture of the
Colles Fracture distal radius
with dorsal
angulation of
the distal
fragment;
sometimes with
ulnar styloid fx
More common in
children and older
Another hyperextension
adults (scaphoid
injury FOOSH fractures are more
common in 15-40 y/o)
Common Fractures:
Colles Fracture
Surgical repair
Common Fractures: Injury fall on
the back of a
Smith Fracture flexed hand
Figure 22-22
Easily missed on
radiograph: look for the
posterior fat-pad sign
Caused by a fall on an
outstretched arm or
direct blow to the elbow Most common elbow
fracture in adults
Figure 22-27. Fracture of radial head with joint effusion, frontal (A)
and lateral (B) views. Radial head fractures (closed white arrows) are
the most common fractures of the elbow in an adult. Look for fat
appearing as a crescentic lucency along the dorsal aspect of the distal
humerus (open white arrow) caused by intracapsular, extrasynovial fat
that is lifted away from the bone by swelling of the joint capsule due to a
traumatic hemarthrosis-the positive posterior fat-pad sign. Virtually all
studies of bones will include at least two views at 90 angles to each
other, called orthogonal views. Many protocols call for two additional
oblique views, which enable you to visualize more of the cortex in profile.
Common Fractures:
Boxer Fracture
Usually a result of
punching a solid object
Figure 22-24
Common Fractures:
Hip Fractures
There are more than 300,000
hip fx in US every year &
incidence is on the rise!
Risk factors
OSTEOPOROSIS (and all of
its risk factors)
Age (incidence doubles with
each decade beyond 50)
High energy trauma or
pathologic fractures in the
young
Common Fractures:
Hip Fractures
Most hip fractures are
in the femoral neck or
the intertrochanteric
region
Fx line may be
difficult to see in a
patient with
osteoporosis
AP Pelvis is the
best initial view to
look for hip
fractures
MRI is best
to detect
occult
fractures
Here, the left femoral neck
fracture cannot be seen on
the AP hip view
Incomplete
loss of
contact
between
articular
surfaces
PIP subluxation
Joint Injury Terminology:
Dislocation
Complete
loss of
contact
between
articular
surfaces
PIP dislocation
Joint Injury Terminology:
Dislocation
Dislocations
are described
by the
position of
the distal
bone(s)
Posterior elbow
dislocation
Extreme Example Bilateral Hip
Dislocation
This
would
require
violent
trauma,
such as
an MVA
Posterior
dislocation
Anterior
dislocation
Shoulder Dislocations are much
more common
The shoulder is a
highly mobile joint &
the most common
joint to dislocate
Most shoulder
dislocations (95%)
are anterior
Special views can be
ordered
Normal shoulder
Posterior shoulder Anterior shoulder
dislocation: humeral head dislocation: humeral head
might appear superior to appears inferior to glenoid
glenoid cavity on AP film cavity on AP film
Non-traumatic Skeletal
Pathology
Osteoarthritis (OA)
Most common joint disease
Presents clinically as pain, deformity, &
limited ROM
Most common cause of disability after age
65
Almost all patients >65 will have
radiographic signs of OA (although not
necessarily clinical signs)
Radiographic Signs of OA
Asymmetric joint space narrowing
Sclerotic bone changes (more dense)
Degenerative cysts (more lucent)
Osteophyte formation (bone spurs)
Note the joint space
narrowing at the DIP
joints
A: DIP, 1st
metacarpal-
Q: What joints are most carpal, hips,
commonly affected by OA? knees, & spine
Note the
medial joint
space
narrowing on
this left knee
radiograph.
This
asymmetric
joint space
narrowing is
typical for OA.
Note the
asymmetric
joint space
narrowing and
sclerosis
around the
joint. The
arrow is
pointing to an
osteophyte.
Q: What is it?
Q: What is it?
Osteoarthritis of the
spine
Figure 24-7
Rheumatoid Arthritis (RA)
Inflammatory arthritis
Joints can become painful, swollen,
deformed, with morning stiffness
Most commonly affects the MCP, wrist,
and PIP joints
DIP joints usually not involved
Radiographic Signs of RA
Symmetric joint
space narrowing
Periarticular
osteopenia or
osteoporosis
Osseous erosions
MCP subluxation
(which causes the
ulnar deviation seen
clinically, a late
finding)
This is the classic look of severe RA
on radiograph of the hands, with MCP
subluxation and osteoporosis.
OA vs. RA
OA vs. RA
OA vs. RA
Optional ReadingChapter 23
of Textbook
An approach to arthritis, covers other
types of arthritis such as
Gout
Calcium pyrophosphate deposition disease
Charcot arthropathy (neuropathic joint)
Psoriatic arthritis
Bone Tumors
This is a
Sharply marginated lesions are malignancy, an
usually benign. This is an osteosarcoma of
enchondroma. the femur.
Bone Tumors
Which of these is probably cancer?
Bone Tumors
Aggressive renal
cell carcinoma that
has metastasized to
the humerus
Osteomyelitis
Focal
destruction of
bone by
infection
Acquired by
hematogenous
spread,
contiguous
This is the classic lytic-sclerotic
spread, or direct look on conventional radiograph,
inoculation but this case has been developing
for a few months.
Osteomyelitis
Osteomyelitis of
the 2nd metatarsal
in a diabetic
Findings on
conventional
radiograph will
not be seen for 10-
14 days, if then
Figure 21-25
Osteomyelitis
Q: What imaging
modalities would be better
for diagnosing
osteomyelitis?
Multiple Myeloma
Multiple myeloma is the most common
PRIMARY bone malignancy. What is the
most common bone malignancy overall?
Q: Getting skull
films on these
patients was a
waste of time.
Why?