Inflammatory Conditions Flashcards

(30 cards)

1
Q

What other condition can polymyalgia rheumatica be linked with?

A

Giant Cell Arteritis

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2
Q

What are the Sx of Polymyalgia Rheumatica?

A
Subacute or rapid onset
Proximal joints: SHOULDERS & PELVIC GIRDLE
B/L aching & tenderness
Morning stiffness
Tenosynovitis
Fatigue
Fever & weight loss
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3
Q

How is Polymyalgia Rheumatica investigated?

A

Bloods: ↑CRP, ↑ESR > 40, CK (N), ↑ALP

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4
Q

How is Polymyalgia Rheumatica managed?

A

Prednisolone: 15mg OD PO for >2years
PPI & Bisphosphonate
IV Methylpred for rapid relief

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5
Q

What are the types of Large vessel vasculitis?

A

GCA

Takayasu’s

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6
Q

What are the types of Medium vessel vasculitis?

A

Kawasaki

Polyarteritis Nodosa

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7
Q

What are the types of Small vessel vasculitis?

A

ANCA +ve: Churg-Strauss, Microscopic polyangitis

ANCA -ve: HSP, Goodpasture’s

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8
Q

What are the types of variable vessel vasculitis?

A

Bechet’s

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9
Q

How does the Chapel Hill Consensus Conference classify vasculitides?

A
  • Infective: Direct invasion of pathogens into vascular wall = inflammation
  • Non-infective: Autoimmune
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10
Q

How does small vessel vasculitis present?

A
Palpable purpura- may become confluent → plaques +/- ulcers
Papules
Urticaria
Vesicles
Splinter haemorrhages
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11
Q

How does medium vessel vasculitis present?

A
Nodules
Ulcers
Digital infarcts
Lived Reticularis (mottled purplish lace-like discolouration of skin)
Papulo-necrotic lesions
HTN- damaged renal vessels
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12
Q

How does large vessel vasculitis present?

A

End organ damage: TIA, CVA, HTN, CVD
Aneurysm
Dissection +/- haemorrhage

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13
Q

How is vasculitis investigated?

A

Imaging: ANGIOGRAPHY +/- BIOPSY
Bloods: ↑ESR, ↑CRP, ANCA, RF, Hepatitis serology
Urine: MSC

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14
Q

How is vasculitis managed?

A

Steroids:
ImmunoS: Cyclophosphamide for s/m vessel disease
ANCA +ve: Mycophenolate

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15
Q

What are the complications of vasculitis?

A
CNS infarct
LT steroid use
AV thrombosis
Gangrene of digits
Pulm haemorrhage
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16
Q

What is dermatomyositis?

A

AI mediated inflammation of striated muscle causing symmetrical proximal muscle weakness & skin lesions

17
Q

What are the causes of dermatomyositis?

A
Idiopathic
OR
Associated: 
CT disease
Malignancy (Ovarian, breast, lung)
18
Q

How does dermatomyositis present?

A

Proximal muscle weakness & tenderness
Photosensitivity
Macular rash: Itchy/burning Back + shoulders = SHAWL sign
Heliotrope rash: Lilac periorbital region w/oedema
Gottron’s papule: Rough, red papules over extensor surfaces of fingers/elbows/knees
Nail fold capillary dilatation

19
Q

How is dermatomyositis investigated?

A

Bloods: ANA +ve, Anti-Mi2, ↑↑CK, ↑AST ↑LDH
Biopsy: Skin & smooth muscle

20
Q

How is dermatomyositis managed?

A

Prednisolone

Photosensitivity: Hyroxychloroquine

21
Q

How is dermatomyositis differentiated from polymyositis?

A

Poly = ↑Anti-Jo1

Same as dermatomyositis but NO rash

22
Q

What is the pathophysiology of gout?

A

Renal re-absorption of urate & poor excretion = supersaturation
Deposition of monosodium urate crystals in & near joints
Crystals interact w/phagocytes & trigger inflammatory response
Over time forms tophi
Leads to acute monoarthropathy & severe joint inflammation

23
Q

What are the RFs for gout?

A
↑Purine diet
OH-
Surgery
Starvation
CKD
Diuretics
Infection
Male
24
Q

Where does gout commonly affect?

A
MTP OF BIG TOE
Ankle
Foot
Wrist
Knee
Elbow
Hand
25
How does gout present?
ACUTE SEVERE pain: Crescendo over 6-12hours Localised Swollen, tender, erythematous joint Fever Malaise Atypical: Tensosynovitis + Bursitis + Cellulitis
26
How is gout investigated?
1) Synovial Aspiration: Crystallography = -ve birefringent urate crystals 2) Bloods: ↑↑ESR/CRP, ↑Urate >360 Xray: Chondrocalcinosis Early = soft tissue swelling Late = punched out lesions
27
How is gout managed?
``` ACUTE: Self-limiting 7-10days 1) Analgesia: NSAIDs (Naproxen) +/- PPI 2) Colchicine PO 3) Prednisolone: PO 1mg/kg as single dose ``` ONGOING: 1) Allopurinol 100mg PD ↑ according to urate levels 2) NSAIDs 3) Febuxostat
28
What is Pseudogout?
Calcium pyrophosphate deposition
29
How is pseudogout investigated?
Joint aspiration: Birefringent rhomboid shaped crystals Xray: Cartilage calcification Bloods: Ca2+, PTH, ALP
30
How is Pseudogout managed?
``` MONO: 1) IA Steroid injection +/-Paracetamol +/- NSAIDs 2) Colchicine Ongoing: Joint replacement ```