SM 249a - Vasculitis Flashcards

1
Q

What is the treatment for anti-GBM disease?

A

Plasmapheresis, glucocorticoids, cyclophosphamide

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

List the immune-complex small vessel vasculitides

A
  • Anti-GBM
  • IgA Vasculitis
  • Cryoglobulinemia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Describe the pathologic findings associated with GPA

A

Granulomatosis with Polyangiitis (GPA)

  • Necrotizign granulomas
  • Few or no immune deposits
  • Associated wtih c-ANCA/PR3+
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Describe Polyarteritis Nodosa

  • “Typical patient”:
  • Arteries affected:
  • Presentation:
A

Polyarteritis Nodosa

  • “Typical patient”: Male 40-60 years old
    • But can affect people of any age
  • Arteries affected: Medium-sized muscular arteries, often at branch points
  • Presentation:
    • Cutaneous
      • ​Nodules, purpura, livedo, retucularis, ulcers
    • Renal disease
    • Neuropathy/Myalgia/Weakness
    • Mesenteric Ischemia
      • “Stomach pain after large meals”
    • Orchitis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe Cryoglobulinemia

  • “Typical Patient”:
  • Arteries affected:
  • Presentation:
A

Cryoglobulinemia

  • “Typical Patient”: Person with MGUS, B-cell malignancy, chronic Hep C, Hep B, HIV, or autoimmune disease
  • Arteries affected: Small vessels (immune complex mediated)
  • Presentation:
    • Digital ischemia
    • Livedo reticularis and skin necrosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What pathologic findings are associated with microscopic polyangiitis?

A

Necrotizing arteries

Few or no immune deposits

No granulomatous inflammation (will be present in GPA)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Does this statement apply to Giant Cell Arteritis, Takaysu Arteritis, or both?

Age of onset <40 years old

A

Takayasu Arteritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Does this statement apply to Giant Cell Arteritis, Takaysu Arteritis, or both?

Affects large vessels

A

Both

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Which vasculitis does this statement apply to?

Frequent URI

A

Granulomatosis with polyangiitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How is GCA treated?

A
  • High dose corticosteroids
  • Tocilizumab (an anti IL-6 antibody)

Treat immediately (while waiting for biopsy) to prevent vision loss!

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Which vasculitis does this statement apply to?

Most patients present with oral and genital ulcers

A

Behcets

Occurs most commonly in patients of Mediterranean, Middle Eastern, and Far Eastern descent

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Describe the treatment for granulomatosis with polyangiitis and microscopic polyangiitis

A

Steroids

+ Rituximab or cyclophosphamide if severe

+ Methotrexate if not severe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How is GCA diagnosed?

A
  • Labs
    • Elevated ESR, CRP
    • Thrombocytosis maybe
  • Imaging
    • Termporal artery ultrasound
    • PET
  • Biopsy
    • Temporal artery
    • Should be done urgently in all patients with suspected GCA
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Which vasculitis is associated with chronic HepC infection?

A

Cryoglobulinemia type 2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Does this statement apply to Giant Cell Arteritis, Takaysu Arteritis, or both?

Constitutional symptoms

A

Both

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Describe granulomatosis with polyangiitis

  • “Typical patient”:
  • Arteries affected:
  • Presentation:
A

Granulomatosis with Polyangiitis (GPA)

  • “Typical patient”: Caucasian 40-50 y/o or >70 y/o
  • Arteries affected: Small to medium vessel vasculitis
  • Presentation:
    • Associated wtih c-ANCA/PR3+
    • Upper airway disease
      • Saddle nose deformity, sinus nodules
    • Pulmonary disease
      • Cavitary lung nodules
    • Glomerulonephritis
      • Crescents
    • Arthritis/arthralgia
    • Neuropathy
    • Ocular disease
    • Vascular
      • Gangrene, venous thrombosis
    • Skin
      • ​Oral ulcers, purpura, nodules
    • Cardiac
    • GI
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is the treatment for Kawasaki disease?

Why is it important to identify and treat early?

A

Aspirin + IVIG

Prevent heart disease/aneurysm later in life

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Does this statement apply to Giant Cell Arteritis, Takaysu Arteritis, or both?

Bruits

A

Takayasu Arteritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Describe Bechets Syndrome

  • “Typical Patient”:
  • Arteries affected:
  • Presentation:
A

Bechets Syndrome

  • “Typical Patient”: 20-30 year old person of Mediterranean, Middle Eastern, or Far Eastern descent
  • Arteries affected: Any! Variable vasculitis
  • Presentation:
    • Oral ulcers
    • Genital ulcers
    • Other cutaneous lesions
    • Ocular involvemnt
    • Arthralgia
    • Neurologic
    • GI
    • Inner ear
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Describe the clinical presentation of Eosinophilic Granulomatosis with Polyangiitis (EGPA)

A

3 phases

  • Prodrome
    • Asthma, allegic rhinitis, nasal polyp
  • Eosinophilic phase
    • Tissue and periphery
  • Vasculitic phase
    • Cutaneous
    • Cardiac
    • Neurologic
    • Renal
    • Gastroenteritis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What are the three ANCA-associated vasculitides?

A
  • Microscopic polyangitiis
  • Granulomatosis with polyangiitis
  • Eosinophilic granulomatosis with polyangiitis
22
Q

Which vasculidities affect medium vessels?

A

Polyarteritis Nodosa

Kawasaki Disease

23
Q

Describe giant cell arteritis

  • “Typical patient”:
  • Arteries affected:
  • Presentation:
A

Giant Cell Arteritis

  • “Typical patient”: Elderly Scandinavian woman
    • Can also occur in men, but more common in women
  • Arteries affected: Large vessels; cranial or extracranial involvement
  • Presentation:
    • New headache
    • Constitutional symptoms
    • Jaw claudication
    • Partial or complete loss of vision
24
Q

Which vasculitis does this statement apply to?

Presents most commonly in children <5

A

Kawasaki disease

25
What are the pathologic hallmarks of Kawasaki disease?
* Affects coronary arteries * Destruction of luminal endothelial cells, elastic lamina, smooth muscle cells * -\> Arterial walll dilation +/- aneurysm formation
26
What complications are associated with Takayasu arteritis?
Aortic regurgitation and acute MI
27
Which arteritis is associated with jaw claudication, new headache, and partial or complete loss of vision?
Giant cell arteritis
28
Describe the treatment for Takayasu arteritis
* High-dose corticosteroids * Methotrexate or Azathioprine * Surgical bypass * Angioplasty +/- stenting has poor outcomes
29
Which vasculitis does this statement apply to? ## Footnote **Associated with p-ANCA/MPO+**
Microscopic polyangiitis *EGPA has p-ANCA/MPO in 40% of cases, but otherwise ANCA(-)*
30
Which vasculitis does this statement apply to? ## Footnote **Treat with aspirin and IVIG**
Kawasaki
31
Describe the pathologic findings associated with polyarteritis nodosa
* Transmural inflammation * No giant cells or granulomas * Common for different phases of vasculitis to occur within different vessels or one vessel at the same time
32
70 yo WM with chronic cough for past year. Exam shows nasal ulcers and lungs with diffuse crackles. * Creat 4.5 * UA with 20 RBCs +casts * c-ANCA + * CXR with small scattered pulmonary nodules * Lung bx shows vasculitis of small peripheral arteries and arterioles. +granulomatous inflammation adjacent to small arterioles What is the most likely diagnosis?
Granulomatosis with polyangiitis 2nd peak in elderly patients, c-ANCA is the key
33
What is the most common form of systemic vasculitis in adults?
Giant cell arteritis
34
What is the appropriate management of a patient for whom you suspect giant cell arteritis?
Ugent temporal artery biopsy Begin treatment with corticosteroids immediately * Biopsy to confirm diagnosis, treat immediately to prevent complications * Vision loss
35
Describe Takayasu Arteritis * "Typical patient": * Arteries affected: * Presentation:
Takayasu Arteritis * "Typical patient": **Asian woman \<40 years old** * Arteries affected: **Aorta, subclavian, carotid** most common * Can affect any artery * Presentation: * **​Constitutional symptoms** * **Unexplained lightheadedness** * **Extremity pain/claudication** * **Bruits** * **Absent/diminshed pulses or BP difference \>10 mmHg**
36
What pathologic findings are associated with Eosinophilic Granulomatosis with Polyangiitis (EGPA)?
ANCA negative most of the tiem
37
Which vasculitis does this statement apply to? ## Footnote **Strawberry tongue**
Kawasaki
38
Which vasculitis does this statement apply to? **p-ANCA +**
Microcsopic polyangiitis
39
Does this statement apply to Giant Cell Arteritis, Takaysu Arteritis, or both? **Affects females \> males**
Both GCA - F\>M = 2:1 Takayasu - F\>M = 9:1
40
Describe the pathological findings associated with Takayasu arthritis
* Granulomatous panarteritis * Intimal hyperplasia * Fixed stenosis and occlusions * Occasional aneurysm
41
Which vasculitis typically presents in children, and is associated with acute onset fever, strawberry tongue, and rash?
Kawasaki Disease
42
Does this statement apply to Giant Cell Arteritis, Takaysu Arteritis, or both? ## Footnote **Age of onset \>50 years old**
Giant Cell Arteritis
43
Describe Anti-GBM disease * “Typical Patient”: * Arteries affected: * Presentation:
Anti-GBM * “Typical Patient”: **Older children and adults** * Arteries affected: **Small vessel (Immune-complex mediated)** * Presentation: * **Acute renal failure** * **Alveolar hemorrhage** * **No constitutional symptoms**
44
Describe Kawasaki Disease * "Typical patient": * Arteries affected: * Presentation:
Kawasaki Disease * "Typical patient": **Asian male child \<5 years old** * **​M\>F 2:1** * Arteries affected: **Medium-sized muscular arteries, esp. coronary** * Presentation: * **Acute onset** * **Fever \> 5 days** * **Rash** (Basically anything except vesicular) * **Extremity edema** * **Involvement of lips and mouth**
45
Which vasculidities affect large vessels?
Takayasu Ateritis Giant Cell Arteritis
46
What vasculitis is associated with MGUS or B cell malignancy?
Cryoglobulinemia Type 1
47
Describe the treatment for polyarteritis nodosa
* Mild * Glucocorticoid monotherapy * MTX or AZA if resistant * Moderate * Glucocorticoid + cyclophosphamide * Viral-associated secondary PAN * Check Hepatitis B * Initiate appropriate antiviral therapy
48
Which vasculitis does this statement apply to? ## Footnote **c-ANCA +**
Granulomatosis with Polyangiitis
49
Describe microscopic polyangiitis * "Typical patient": * Arteries affected: * Presentation:
Microscopic polyangiitis * "Typical patient": **Middle age** * Arteries affected: **Small vessels** * Presentation: * **Glomerulonephritis** * **Pulmonary capillartis** * **Peripheral neruopathy** * **Skin lesions** * **Weight loss** * **Fever** * **p-ANCA/MPO+**
50
Which cytokine is associated with GCA?
IL-6 Treat with tocilizumab
51
Describe Eosinophilic Granulomatosis with Polyangiitis * "Typical patient": * Arteries affected: * Presentation:
Eosinophilic Granulomatosis with Polyangiitis * "Typical patient": **Male 35-45 with new asthma** * **​**Only slight male predominance * Arteries affected: **Small vessels** * Presentation: * **Often ANCA negative** * p-ANCA/MPO+ in 40% of cases * **Eosinophilia/elevated IgE** * **Adult onset asthma** * **3 phases** * **​**Prodrome, Eosiniphilic, Vasculitic
52
Which antigens are associated with p-ANCA and c-ANCA?
p-ANCA = Myeloperoxidase (MPO) c-ANCA = Proteinase 3 (PR3)