Rheumatology Revision 5 Flashcards

1
Q

A 66-year-old man presents to his GP with a 2-day history of pain in his right big toe. He reports having had similar pain on 2 previous occasions but did not seek medical help. His past medical history includes hypertension and hypercholesterolaemia.
On closer inspection, there is a swollen, erythematous 1st metatarsophalangeal joint on the right foot. The rest of the foot examination, and examination of other joints, are unremarkable

The patient is prescribed the first-line medication to prevent future presentations after the flare has settled. What is the most common side effect of this medication?

Vertigo

Jaundice

Constipation

Rash

Fatigue

A

The first-line medication for prevention of gout attacks is allopurinol. Allopurinol should started 2-4 weeks after the acute flare of gout has settled. According to the BNF, a common side effect of allopurinol is rash, in which case the medication should be stopped.
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2
Q

Define juvenile idiopathic arthritis (JIA) [1]

A

Juvenile idiopathic arthritis (JIA) refers to a condition affecting children and adolescents where autoimmune inflammation occurs in the joints. It is diagnosed where there is arthritis without any other cause, lasting more than 6 weeks in a patient under the age of 16.

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3
Q

What are the 5 types of JIA? [5]

A

Systemic JIA - aka Still’s disease.
Polyarticular JIA
Oligoarticular JIA
Enthesitis related arthritis
Juvenile psoriatic arthritis

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4
Q

Describe the clinical presentation of Still’s disease / systemic JIA [+]

A

Systemic illness that can occur throughout childhood in boys and girls. It is an idiopathic inflammatory condition. Usually has:
* Subtle salmon-pink rash
* High swinging fevers
* Enlarged lymph nodes
* Weight loss
* Joint inflammation and pain
* Splenomegaly
* Muscle pain
* Pleuritis and pericarditis

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5
Q

TOM TIP: Think of Still’s disease (systemic JIA) when a patient presents with a salmon-pink rash, fevers and joint pain.

In children that have fevers for more than 5 days, the key non-infective differentials to remember are [4]

A

Kawasaki disease, Still’s disease, rheumatic fever and leukaemia.

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6
Q

How do you investigate for Still’s disease? [4]

A

Clinical picture

Serology:
- ANA and RF negative
- Raised CRP; ESR; platelets and ferritin

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7
Q

Describe a key complication of Still’s disease / systemic JIA? [1]

How does it present? [6]

A

Macrophage activation syndrome (MAS):
- massive inflammatory response

Presentation:
- DIC
- Anaemia
- Thrombocytopenia
- Bleeding
- Non-blanching rash
- Low ESR

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8
Q

Describe the pattern of pyrexia experienced in Still’s disease in adults [1]

A

typically rises in the late afternoon/early evening in a daily pattern and accompanies a worsening of joint symptoms and rash

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9
Q

Tx for Still’s disease (in adults) [2]

A

NSAIDs
* should be used first-line to manage fever, joint pain and serositis
* they should be trialled for at least a week before steroids are added.

steroids
* may control symptoms but won’t improve prognosis

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10
Q

Describe the presentation of polyarticular JIA [2]

A
  • idiopathic inflammatory arthritis in 5 joints or more
  • symmetrical arthritis
  • mild systemic symtpoms

NB - think of it like a seronegative juvinilie RA

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11
Q

Describe the presentation oligoarticular JIA [4]

A
  • It involves 4 joints or less.
  • Usually it only affects a single joint, which is described as a monoarthritis - often knee or ankle
  • Classically associated with anterior uveitis - refer to an opthamologist
  • ANA positive
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12
Q

How can you think of Enthesitis-Related Arthritis? [1]

A

A paediatric version of the seronegative spondyloarthropathy group of conditions that affect adults. These conditions are ankylosing spondylitis, psoriatic arthritis, reactive arthritis and inflammatory bowel disease-related arthritis.

The majority of patients with enthesitis-related arthritis have the HLA B27 gene.

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13
Q

Describe the managment of juvenile idiopathic arthrits

A

NSAIDs, such as ibuprofen
Steroids, either oral, intramuscular or intra-artricular in oligoarthritis
DMARDs, such as methotrexate, sulfasalazine and leflunomide
Biologic therapy, such as the tumour necrosis factor inhibitors etanercept, infliximab and adalimumab

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