Paediatric Case Presentation
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Transcript Paediatric Case Presentation
Paediatric Case
Presentation
Natasha Quader ST1
September 2008
Patient CD
8 year old girl
Normally fit and well
PC – Pyrexia
- Lethargy
- Groin and hip pain
History of Presenting Complaint
7/52 ago had pyrexia for 1 week followed by a cough → viral URTI
Intermittent pyrexia - mainly nocturnal spikes
C/o hip and groin pain.
- Present on waking up in the morning
- Pain waking her up during sleeping
- Developed difficulty in walking, pain on weight bearing
Increasingly lethargic – sleeping during the day and missing school
Generally unwell, ↓ appetite, irritable and crying
PMH
PMH
- Laryngomalacia during infancy
- RTA in Feb ’07 – back injury resolved
SH – no recent travel abroad
Immunisations up-to-date
DxH – nil, NKDA
FH – Maternal grandmother with RA
Examination 1
Alert, communicating
PR – 80 regular
Temp – 38 °C
RR-18
Abdomen
Bilateral cervical
lymphadenopathy
Throat – NAD
Ears – wax bilaterally
No rashes
HS I + II + O
Chest: Clear
Inguinal
lymphadenopathy
Lower
abdominal
tenderness
Examination 2
CNS
MSK
CN – NAD. PEARL
No hip/knee joint
Lower limbs bilaterally
swelling
- tone normal
Tenderness over AIS
- power 4/5
and crest bilaterally
- reflexes symmetrical
Hips - ↓ active ROM
Co-ordination – intact
Romberg’s negative
Antalgic gait
Slight waddling and holding R.
inguinal region
Positive Examination Findings
Pyrexic
Lower abdominal tenderness
Bilateral inguinal lymphadenopathy
Bilateral hip tenderness and restricted ROM
Antalgic gait
Differential Diagnosis
Septic hip
Infection – viral, bacterial, Lyme disease
Juvenile arthritis
Malignancy – leukaemia, neuroblastoma
Perthes
Transient irritable hip
Infection Screen
MSU – NAD
Blood cultures – no growth
EBV Igm – negative
Toxopl Igm – negative
ASOT – normal
Rubella Igm – negative
Parovirus Igm – negative
Bilateral Hip X-ray
Imaging
USS abdo and hips – no fluid in hip joints
MRI abdo/pelvis - No evidence of avascular
necrosis
Blood Test Results
Initial
GP
Hb
WCC
Plt
7 weeks
later
8 weeks
In -patient
9.9
6.3
418
9.7
5.5
354
9.7
4.2
338
98
9
90
13
105
9 weeks
Inpatient
10.2
6.1
516
Neut
Lymp
CRP
ESR
104
10 weeks
OPA
14 weeks
OPA
10.2
6.1
516
2.20
2.70
11.1
4.9
295
<1
104
<1
14
Follow Up
Follow up 10/7 after discharged from Hospital
Symptoms much improved
- no complaints of hip pain on weight bearing
- no pain during sleep
- no pyrexia for 5/7
- analgesia reduced from QDS to ON
- generally more mobile, active and cheerful
Follow up Results
On examination
- discomfort on extreme range of full
abduction of R. hip
- Tearful on jumping on 2 feet
Repeat bloods: ESR remains high – 104
Anti nuclear antibody positive
Referral → Rheumatologist
→ Ophthalmologist
Juvenile Arthritis
Is a group of conditions
in which there is chronic arthritis
lasting more than 6 weeks,
presenting
before 16 years of age
Classifications
Systemic illness (Still’s disease)
- 20%
Rh factor negative polyarticular
- 25%
Rh factor positive polyarticular
- 5%
Pauciarticular arthritis assoc with ANA
& chronic uveitis - 30-35%
Pauciarticular arthritis assoc with spondylitis
and HLA B27 - 10-15%
Aetiology
Autoimmune disease in which the cause of arthritis is
largely unknown
A possible viral aetiology has been considered for a
variety of arthritis conditions and clustering of
patient’s following viral epidemics
Viral infections that have noted include mumps,
rubella and Parvovirus B19
Pauciarticular Arthritis
Female > Male
Involvement of up to 4 or fewer joints – typically
larger joints such as the knee
3 subtypes:
1) The early onset form (< 5 years of age), involves
most frequently knee joints
2) The late onset form ( > 9 years of age) most
frequently involves hips with/without sacroilitis
3) Develops at any age with an asymmetrical
oligoarthritis, dactylitis and psoriatic manifestation
Pauciarticular Arthritis 2
Is a large association with Anti Nuclear
Antibodies between 40-75%
Frequently associated with chronic anterior
uveitis (can be asymptomatic or asso pain,
light sensitivity and redness)
Regular opthalmological screening is indicated
Complications
Chronic anterior uveitis – if poorly controlled may
result in permanent eye damage, including blindness
Flexion contactures of the joint – joint held in the
most comfortable position, thereby minimising intraarticular pressure. Chronic disease can lead to joint
destruction and need for joint replacement
Growth failure – anorexia, chronic disease and
steroid therapy
Amyloidosis – rare complication causing proteinuria
and renal failure
Management 1
Multidisciplinary approach is required for
optimal Rx: - relieve pain
- preserve joint function
- maintain normal growth and
psycho – social development
Physiotherapist & Occupational Therapists
- strengthen muscles & keep joints flexible
- encourage normal limb development
- maintain function and prevent deformities
- develop exercise programs
Management 2
Paediatricians, Rheumatologist and Nurses
- educating child and family
- medical management
Counsellor
– for the child and their family to reduce anxiety
and share management of disease
Medical Management
NSAIDS – aspirin, ibuprofen, diclofenac
DMARDS (Disease modifying anti rheumatic drugs)
- under rheumatologist’s supervision
- hydroxychloroquine, penicillamine, methotrexate
Intra-articular corticosteroid injections
Corticosteroids
– severe systemic involvement &/or for eyes Rx
TNF alpha blockers
– block the immune protein TNF (inflammatory agent in
arthritis)
Prognosis
Symptoms usually go away after a few years
There are usually no further recurrences
Some children may have longer lasting
involvement
References
Laura Quarte et al. Juvenile idiopathic arthritis: An update on
clinical and therapeutic approaches. Ann Ital Med Int 2005; 20:
211-217
Juvenile Rheumatoid Arthritis
http://www.emedicine.com/ped/topic1749.htm
Juvenile Rheumatoid Arthritis
http://www.emedicinehealth.com/juvenile_rheumatoid_arthritis
/article_em.htm
Arthritis in children
http://www.medicinenet.com/juvenile_arthritis/article.htm