RHEUMATOLOGY Flashcards
Variations of normal posture
Flatfoot, bow legs, knocked knees, in-toeing, out-toeing, toe walking
Bow legs will be considered normal until the age range of?
1-3 years
Normal age range of knocked-knees
2-7 years
Flat feet?
Foot arch is lost
Normal age range of flat-feet
1-2 years.
In-toeing normal age range
1-2 years
Out-toeing normal age range
6-12 months
Toe walking normal age range
1-3 years.
Hypermobility should be a suspicion in what abnormal postures?
Flat feet, out-toeing.
What abnormal posture can be seen in autism?
Toe-walking
Knocked knees can be seen in?
Juvenile idiopathic arthritis
DDs to consider in toe-walking
Spastic diplegia, muscular dystrophy, JIA, cerebral palsy, autism
Which abnormal postures can be seen in Marfan syndrome
Out-toeing.
Congenital talipes equino varus also known as
Club foot
Ideally when should club foot be diagnosed
Before discharging after birth head to the examination
T/f
1. Club foot is mostly seen in males
2. Club foot affects both feet in all cases
3. Oligohydramnios can cause club foot
4. Club foot is also associated with calf atrophy and hip problems.
5. Club foot should be radiologically diagnosed & confirmed
6. Club foot should be surgically corrected always.
- T
2.f - T
- T
- F
- F
Causes of club foot
Twin births
Uterine fibroids
Oligohydramnios
Bone and muscle abnormalities of the child
Other problems in club foot
Calf atrophy
DDH - (development dysplasia of hip)
IX of club foot
X-ray AP & lateral
Mx of club foot
Most children will physiotherapy
Some will need surgical correction - ponseti method (serial casting)
Clinical dx of club foot
Foot cannot be flexed enough to touch the shin and extended back to it’s normal anatomical position
Perthe’s disease is?
Avascular necrosis of the head of femur
Perthe’s disease is associated with
DDH
Mucopolysaccharoidosis
Achondroplasia
Rickets
Protein C & S deficiency- blood clots
T/f
1. Perthe’s is seen mostly in males
2. Perthe’s involves both femurs.
3. Perthe’s should be surgically corrected.
4. There is a painless limp in Perthe’s
5. There is a delayed bone growth in Perthe’s
- T( 5:1)
- F (20% bilateral)
- F (not always)
- T (can become painful )
5 T
Classic age of presentation of Perthe’s disease
Around 7 years
What movements of the hip joint is limited in Perthe’s disease
Internal rotation
Abduction
Mx of avascular necrosis of the hip
Mainly non surgical
Physiotherapy & decreased activity
Devices
Surgery
Pre-pubertal obese boy presents with painful gait. Dx?
Slipped upper femoral epiphysis ( SUFE)
Classic age of presentation of SUFE
12-15 years. (During growth spurt )
SUFE can be associated with?
Hypothyroidism
Increased growth hormones
Reduced sex hormones
Renal osteodystrophy
SUFE children presents with
Painful gait
Externally rotated leg
What happens in SUFE
Head & neck of the femur is separated
Mx of SUFE
Pin fixation in-situ (surgery)
T/f about transient synovitis
1. There is an antibody reaction in the hip joint in transient synovitis.
2. Fluid accumulated in the hip joint can be seen in X-ray
3. Child will present with a mild fever and limping
- T
2.F - T
What tests will be normal in transient synovitis
FBC
CRP
Mx of transient synovitis
PCM
Bed rest
How long will it take for transient synovitis to resolve
Within 1 week but some may lead to perthe’s
Septic arthritis age of presentation
<2 years
T/f about septic arthritis.
I. Usually 2 joints are affected.
2. Staphylococcus aureus spreads hematogenously
3. They present with high fever.
4. The affected joint will be erythematous and non-tender
5. WCC is high
6, antibiotics should be given for 4-6 months
7. Ultrasound can be used for DX joint effusions.
8. Septic arthritis can be fatal.
- F (one joint)
- T
- T
- F (tender)
- T
- F (4-6 weeks)
- T
- T
Presentation of septic arthritis
Erythematous, tender, warm joint with reduced range of movement in an acutely unwell, febrile child. Infant may hold the limb still (pseudoparalysis) and cry if it is moved
Ix and findings of septic arthritis
WCC high
ESR high
Ultrasound → to identify effusions
Blood culture
Treatment of septic arthritis
Joint aspiration and 4-6 weeks antibiotics.
Can you send the child home with oral antibiotics once joint aspiration was done for septic arthritis
Nope. Intravenous antibiotics needed initially
Difference between Transient synovitis and septic arthritis
Transient synovitis first septic arthritis second
Onset- Acute limp, non- weight bearing
Acute onset, non- weight bearing
Fever- Mild/ Absent
Moderate/high
Child’s appearance- looks well
looks ill
Hip movement- comfortable at rest, limited internal rotation, pain on movement
Hip held flexed, severe pain at rest and worse on any attempt to move joint
WCC - normal
high
ESR- normal
high
USS- fluid in joint in both
Radiograph- normal
normal/ wide joint space
Mx- rest, analgesics
Joint aspiration w USS guidance
Prognosis- resloves <1 week, some may go into perthe’s
Progressive and severe joint damage if not treated
MOs that cause osteomyelitis
Staph aureus
Group A beta hemolytic streptococcus
MO method of spread in osteomyelitis
hematogenous
C/F of osteomyelitis
Pseudoparalysis
erythema and swelling in hip
Part of the bone affected in osteomyelitis
Metaphysis
Ix of osteomyelitis
Increased CRP, ESR, WCC
Xray will take around 1-2 weeks to show
USS/bone scan/MRI
Rx of osteomyelitis
IV Abx for 4-6 weeks
Cloxacillin, Flucloxacillin, Vancomycin, Fusidic acid
Rx of osteomyelitis of the hip
Emergency surgery
JIA is seen in
<16 year olds
JIA is arthritis persisting for more than….
6 weeks
Subtypes of JIA
Monoarticular
Oligo/ Pauci articular (<4)
Polyarticular(>5)
Systemic
JIA is seen more in Females than males in….. subtypes
Oligo
Poly
JIA is seen equally in males and females in…. subtypes
Systemic
Poor prgnosis of JIA is associated with
Polyarticular and RF+
Pauciarticular can be associated with
chronic iridocyclitis
Characteristic rash seen in JIA
Salmon pink evanescent rash which only appears when the fever is present
JIA extra- articular manifestations
Hepatosplenomegaly
LN enlargement
Pluritis/ Pericardial effusion
Ix done for JIA
ANA
RF
CBC- High Plt, WCC, Low Hb
High ESR
High Sr. Ferritin
High CRP
Mx of JIA
NSAIDs
Steroids
DMARDs
SLE typical Sx
Arthritis
Malaise
Malar rash- photosensitive
Ix done for SLE
ANA+
ds DNA +
ESR High
Pancytopenia
CRP normal
Juvenile dermatomyositis Sx
malaise
progressive weakness
heliotropic rash
myalgia
skin hypertrophy in MCP, PIP joints
arthritis
Ix for juvenile dermatomyositis
High ESR
High CPK ( creatine phosphokinase)
The rashes seen in juvenile dermatomyositis
Malar
Heliotropic ( around eyelids)
Heliotropic more common than malar
Mx of juvenile dermatomyositis
Steroids
Recurrent fractures and blue sclera. Dx
Brittle bone disease
Osteogenesis imperfecta is also known as
Brittle bone disease
The issue in Brittle bone disease
Disorder of collagen metabolism causing fragile bones
Most common form on brittle bone disease
Type 1 (AD)
Mx of brittle bone disease
Bisphosphonates
Marfan syndrome is
AD
Sx of marfans
Tall stature
Long thin digits ( arachnodactyly)
Hyperextensible joints
High arched palate
upward dislocation of the lens
severe myopia
Arm span> height
Deformities that might be seen in marfan
Chest- pectus excavatum, carinatum
Scoliosis
Major CVS complication in marfan
Mitral valve prolapse, regurgitation
Aneurysm of the aorta
Ix for marfans
Echo
eye referral
highest chance of JIA to have ANA positive tests
Oligoarticular
Most likely to be both ANA and RF negative
Systemic JIA
Intra- articular steroids are most likey used in
Oligoarticular JIA
serial casting for club foot is known as
Ponsetti method
MCC of acute hip pain in children is
Transient synovitis
salmonella osteomyelitis is associated with…. anemia
Sickle cell
Most common bone involved in acute osteomyelitis
Distal femur or proximal tibia
MCC of acute arthritis in children is
reactive arthritis
MCC of chronic arthritis in children is
JIA
Most serious complication in neonatal lupus is
Heart blocks
Gottron’s Papules
Skin hypertrophy over the MCP, PIP joints
CKPA is elevated in dermatomyositis
due to myositis
life threatening complications in dermatomyositis
Respiratory failure
Cardiac failure
Aspiration pneumonia