Paeds MSK Flashcards

1
Q

Rickets

inadequately mineralised bone in developing and growing bones.

  • Soft and easily deformed bones
  • Often due to VitD deficiency in adults: Osteomalacia
  • Dietary deficiency, Prolonged breast feeding, Unsupplemented milk formula, lack of sun light are major causes
A
  • Miserable child
  • Aching bones and joints
  • Bow legs - toddlers
  • Genu Valgum - Knock Knees
  • Rickety Rosary - swelling at wrist joint
  • Soft skull in early life - craniotabes
  • Kyphoscoliosis

Bloods Low VitD, Serum Calcium. Raised Alk phosphatase

Management: Oral Vit D

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2
Q

Brittle Bone Disease | Autosomal Dominant

Osteogenesis Imperfecta

disorder of collagen metabolism resulting in bone fragility & fractures

A
  • Fractures from minor trauama
  • Blue Sclera
  • Deafness 2ndry to Otosclerosis
  • Dental Imperfections

Management
- Underlying condition cannot be cured.
Medical treatment includes:
- Bisphosphonates to increase bone density
- Vitamin D supplementation to prevent deficiency

all relevant bloods for bones are normal.

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3
Q

Irritable Hip

Transient Synovitis

Acute pain following viral infection

Most common hip pain in children b/ween 3-8Y

A
  • Limp/ Refusal to weight bear
  • Pain in hips and/or groin
  • Low grade fever

Management
- Self limiting

High grade fever should point towards a septic arthritis cause.

children may be monitored in primary care (with a presumptive diagnosis of transient synovitis)

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4
Q

M:F ratio = 2:1

Septic Arthritis

Infection of joint space by bacteria or fungi. Beyond neonatal period

Most common: Staph Aureus so important to perform joint aspiration to see.

A
  • Joint pain often unilateral
  • Limp
  • High grade fever with lethargy
  • Swollen Red Joint with minimal movement

Management
- Antibiotics started promptly and adjusted according to culture results.

The most commonly affected joints are the hip, knee and ankle.

The Kocher criteria for the diagnosis of septic arthritis:
fever >38.5 degrees C
non-weight bearing
raised ESR
raised WCC

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5
Q

Infection of the metaphysis of long bones. often femur or tibia

Osteomyelitis

Infection of the bone.

  • Staph Aureus most common
  • Salmonella species dominate in sickle cell.
A
  • low-grade pyrexia or malaise; may possibly be afebrile.
    Once infection becomes established in a bone, it presents with a markedly painful, immobile limb in a child with acute febrile illness.
  • Haematogenous spread common in children results from bacteraemia

MRI investigation of choice

Management
- Flucloxacillin 6wks
- Clinamycin if penicillin allergy

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6
Q

M 5:1 F

Perthe’s Disease

Degenerative hip joints in children due to avascular necrosis of femur

  • Specifically the femoral epiphysis. Impaired blood supply to the femoral head causes bone infarction.
  • often unilateral
A
  • Hip pain, stiffness and limp
  • XRay: widening of joint space, decreased femoral head size
  • Technetium bone scan if XRay clear.

can lead to osteoarthritis

Treatment involves physiotherapy initially to optimise range of movement. Sometimes surgery is required in severe disease.

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7
Q

obese boys - 10-15y

Slipped capital femoral epiphysis

Hip condition, displacement of femoral head epiphysis postero-inferiorly

May present acutely following trauma or more commonly with chronic, persistent symptoms

A
  • hip, groin, medial thigh or knee pain
  • Sometimes following trauma
  • loss of internal rotation of the leg in flexion
  • bilateral slip in 20% of cases

AP + lateral Xray = Diagnostic

  • Management is primarily surgical stabilisation, usually with pin fixation in situ - single cannulated screw in middle of epiphysis.
  • Physiotherapy following surgery is essential to optimise the range of movement and return to normal activities.
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8
Q

Osgood Schlatter

type of osteochondrosis

Repetitive strain from overuse of the knee can increase risk.

A
  • inflammation at tibial tuberosity
    • Pain in the anterior aspect of the knee
  • Pain exacerbated by physical activity, kneeling and extension of the knee
  • commonly unilateral

inflammation @ growth plate site.

  • Reduction of physical activity
  • Ice
  • NSAIDs
  • Physio
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9
Q

Congeital dislocation of Hip

Developmental dysplasia of the hip

sublaxation through to frank dislocation of the hip.

RF: Female, Breech Presentation, Oligohydraminos
More common at Left hip

A

Symptoms: - Different leg lengths, Restricted hip abduction on one side.

Examination: Barlows test(dislocate femoral head) Ortolani(Relocate dislocated head)

USS 1st line. if older than 4.5m then Xray

Management
* most unstable hips will spontaneously stabilise by 3-6 weeks of age
* Pavlik harness (dynamic flexion-abduction orthosis) in children younger than 4-5 months
* older children may require surgery

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10
Q

Juvenile idiopathic arthritis

Arthritis in U16 for more than 6wk

A
  • pyrexia
  • salmon-pink rash
  • lymphadenopathy
  • arthritis
  • uveitis
  • anorexia and weight loss

ANA +ve. RF -ve

Cannot be cured, but early aggressive control of inflammation improves long-term outcomes.
Medical management includes:
- NSAIDs and analgesia
- Methotrexate – less effective in Still’s disease.
- Corticosteroids – either oral, intramuscular or intra-articular in oligoarthritis
- Biologic therapies.

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11
Q

Scoliosis

Risk factors : +VE fam history, connective tissue disorders(Marfans)

Causes of scoliosis are:
- Idiopathic: most common cause, either early onset (less than 5) or late onset, mainly girls aged 10-14 years
- Congenital: congenital structural defect of the spine
- Secondary: related to other disorders such as neuromuscular problems, bone or connective tissue disorders, arthritis etc.

A

Lateral curvature of the spine in the frontal (CORONAL) plane. In most cases the changes are mild, pain free and mainly a cosmetic problem; however severe can lead to further complications.

  • Mild disease will resolve spontaneously, or progresses minimally.
  • Severe cases are managed in specialist spine centres where non-medical treatment such as bracing is considered.
  • Surgery indicated only if severe, or there is coexisting pathology such as neuromuscular or respiratory disease.
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12
Q

Torticolis

Common cause is sternocleidomastoid tumour

Torticollis – wry neck. Tends to be a problem with the muscles of the neck that cause the head to tilt down.

A
  • Congenital condition tends to present with a mobile, non-tender nodule which can be felt within the body of the sternocleidomastoid muscle. May be restriction or head turning and tilting of the head.
  • Resolves it self 2-6mths
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