Lymphoid/Rheum IM Flashcards

1
Q

How to differentiate autoantibodies in testing of rheumatic conditions?

A

Ab against Nuclear antigens (ANA)
Ab against cytoplasmic antigens (ANCA)

Diagnosis of individual conditions can be further supported by detecting disease-specific ANAs or ANCAs

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2
Q

Examples of conditions where there are specific ANCAs?

A

Granulomatosis with polyangiitis (and a few other polyangiitis)
Primary Sclerosing Cholangitis
Ulcerative Colitis

ANCAs observed in especially vasculitides

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3
Q

Examples of conditions where there are specific ANAs?

A

SLE = Anti-dsDNA
Systemic Sclerosis (Scleroderma)
Sjögren syndrome
Polymyositis, dermatomyositis

Generally elevated in connective tissue disorders!

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4
Q

Causes of Reactive neutrophilia?

Reactive is the commonest cause of neutrophilia

A

Acute bacterial infection
Chronic inflammatory state
Bone marrow stimulation
Drugs
Solid organ tumour

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5
Q

What is Stevens-Johnson syndrome / Toxic Epidermal Necrolysis?

A

Skin rxn causing extensive epidermal detachment.

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6
Q

Is Rheumatoid Factor useful as a marker for seronegative arthropathies?

A

No. Rheumatoid factors can be raised in up to 20% of seronegative arthropathies. They can be raised in almost any form of autoimmune inflammation.

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7
Q

How to differentiate mAb drugs, whether human/humanized/chimeric?

A

Mumab = human
Zumab = humanized
Ximab = Chimeric

Chimeric drugs have higher risk of immune response / hypersensitivity

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8
Q

Which 2 cancers does RA raise risk of?

A

Lung cancer
Lymphoma

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9
Q

How to identify lung pathologies due to RA?

From King Julian tutorials - how to compartmentalize differentials

A

Go by compartments!
Parenchyma = inflammation, infection, malignancy
Airway = bronchiectasis,** rheumatoid nodules that can cause obstruction and hence atelectasis**
Interstitium = ILD
VEssels = pulmonary vasculitis
Pleura = pleuritis, pleural effusion

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10
Q

What is Erythema Multiforme?

A

Inflammation of SubQ fat caused by delayed hypersensitivity rxn.
Associated with infection, autoimmune diseases e.g. sarcoidosis, UC etc, pregnancy, OCP
Firm, erythematous nodular rashes over both LL
Bilateral hilar lymphadenopathy

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11
Q

Common genes in SLE?

A

HLA-DR2, HLA-DR3

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12
Q

Skin manifestations of SLE?

A

Malar rash sparing nasolabial folds
Raynaud phenomenon
Photosensitivity causing maculopapular rash
Discoid rash
Oral ulcers
Non-scarring alopecia
Periungual telangiectasia

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13
Q

Common joints affected in SLE?

A

Fingers, carpal joints, knee.
Usually distal symmetrical polyarthritis

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14
Q

Which NSAIDs are known to cause psoriasis flares?

1

A

Indomethacin and Naproxen

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15
Q

What heart valvular disease is Ankylosing Spondylitis associated with?

A

Aortic regurgitation.

Likely due to sclerosing inflammatory process involving aortic root

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16
Q

What are “B” symptoms? In which conditions?

A

Systemic symptoms of LOW, fever, night sweats that are a/w lymphomas and leukemias.

17
Q

Screening vs Diagnostic for SLE?

A

ANA for screening
dsDNA for diagnostic.
Screen with ANA. If +ve, test Anti-dsDNA
Active SLE has low C3 C4 complement levels

18
Q

Commonest cutaneous manifestation of sarcoidosis?

A

Erythema nodosum.
Often comes with bilateral hilar lymphadenopathy

19
Q

CREST syndrome in Scleroderma?

A

Calcinosis Cutis
Raynaud phenomenon
Esophageal hypomotility
Sclerodactyly
Telangiectasia

20
Q

Common triggers of psoriasis?

A

Infection = URTI, staphs, HIV
Mechanical irritation
Drugs

21
Q

5 types of psoriasis?

A

Plaque psoriasis = standard.
Inverse psoriasis = plaques on flexor surfaces
Pustular psoriasis = pustules surrounded by inflamed skin
Guttate psoriasis = small round papules that are raised and sometimes scaly.
Erythrodermic psoriasis = worst type.

22
Q

Presentation of psoriasis? Excluding arthritic part

A

Well-demarcated, scaly, pruritic, erythematous plaques/papules with silver-white scaling
Mainly on extensor surfaces, scalp, trunk, elbows.
Auspitz sign = small telangiectasia when scales are scraped off. Removal of scales expose dermal papillae, causing bleeding
Koebner phenomenon = physical stimuli or skin injury can cause appearance of psoriatic skin lesions on previously unaffected skin

23
Q

Classic DRSAM presentation of Psoriatic arthritis?

A

DIPJ involvement
RA-like
Spondylitis, sacroilitis
Asymmetric oligoarthritis
Mutilans

24
Q

Risk factors for RA

A

HLA-DR4 and HLA-DR1 gene
Smoking
Pre-menopausal women
Infection, obesity, family hx

25
Q

Hand manifestation of RA?

A

Symmetrical (usually) pain and swelling of joints
Swan neck deformity
Boutonniere deformity
Z thumb
Hitchhiker thumb
Ulnar deviation of fingers
Piano key sign
Hammer toe or claw toe
Atlantoaxial subluxation
Rheumatoid nodules

26
Q

Joints commonly affected by RA?

A

MCPJ, PIPJ
Wrist
Knee
MTPJ

27
Q

X-Ray findings of RA?

A

Narrowing of joint space
Thickening of subchondral bone
Subchondral cyst
Osteophytes
Marginal erosion of cartilage and bone
Osteopenia
Soft tissue swelling

28
Q

Triad of reactive arthritis?

A

Arthritis
Conjunctivitis
Urethritis

29
Q

Presentation of REactive Arthritis?

A

Latency of 1-4 weeks
Arthritis can be symmetrical or asymmetrical.
- sacroilitis
- Dactylitis
- Enthesitis
- Arthritis predominantly in lower extremities

30
Q

Diagnostics of Reactive arthritis?

A

Send stool culture.
Check for STI in case of genitourinary chlamydia (Nucleic acid Amplification Test).
Usual bloods e.g. CRP ESR, high TW.
Negative rheumatoid factor or anti-CCP Ab.
Arthrocentesis will show negative gram stain/cultures, no crystals. Just high WBC.

31
Q

XR signs of reactive arthritis?

A

Loss of lumbar lordosis
Ankylosis of costosternal and costovertebral joints
Dagger sign
Bamboo sign

Shiny corners sign

32
Q

Skin manifestations of Dermatomyositis?

A

Heliotrope rash
Gotttron’s papules
V sign
Shawl sign
Mechanic hands

33
Q

What is multiple sclerosis?

A

Chronic degenerative disease of CNS characterized by demyelination and axonal degeneration in brain and spinal cord, caused by an immune-meiated inflammatory process

34
Q

Diagnosis of Dermatomyositis?

A

Mostly clinical diagnosis
Muscle biopsy showing muscle fibre damage

35
Q

How to confirm diagnosis of Multiple Sclerosis?

A

McDonald criteria of both DIT and DIS must be met
Dissemination in Time = Appearance of new CNS lesions over time that can be confirmed clinically, with imaging, or with CSF analysis
Dissemination in Space = Presence of lesions in different regions of CNS that can be confirmed clinically or in MRI

MRI is imaging of choice, showing MS plaques with finger-like radial extensions (Dawson fingers)
Contrast-enhancement of active lesions
CSF exam showing oligoclonal bands in CSF is highly suggestive of MS

36
Q
A