Inflammatory and vaso-oclusive ulcers (Dec 24) Flashcards

(22 cards)

1
Q

What is an inflammatory ulcer?

A

An ulcer where the primary pathologic process is inflammation

e.g.
- Pyoderma Gangrenosum
- Vasculitis
- ulcerative panniculitis
- granulomatous conditions
- manifestation of AICTD

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2
Q

What are the key clinical features of Pyoderma gangrenosum?

(6)

A

Severe pain
Pathergy

Violaceous borders
Undermined edge
Irregular shape
Cribiform scarring

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3
Q

Does PG have any disease associations?

A

~ 50% have an underlying disease

Inflammatory bowel disease
Inflammatory arthritis
Haematological malignancy

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4
Q

What is the role of biopsy in PG?

A

Only 7% of biopsies have characteristic features

More useful to exclude other aetiologies

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5
Q

How is PG diagnosed?

A

No pathgnomonic histopathology findings or tests.

Relies on clinical diagnostic criteria:
- PARACELUSUS
- Delphi
- Su

Paracelusus has the highest sensitivity (JAAD CME Dec 2024)

  • score > 10 for Dx

Major criteria (3 points each)
–> progressive disease course
–> red/ violaceous ulcer border
–> Assessment of ddx

Minor criteria (2 points each)
–> Amelioration by immunosuppressants
–> Characteristically irregular / bizarre ulcer shape
–> extreme pain

Additional (1 point)
–> ass with systemic disease
–> undermined ulcer border
–> histopath with suppurative inflammation

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6
Q

How are vasculidities classified?

A

Small Vessel
1. Immune complex vasculitis
2. IgA Vasculitis
3. Cryoglobulinaemic vasculitis
4. ANCA associated Vaculitis
- Microscopic polyangitis
- Eosinophillic granulomatosis
- Granulomatosis with polyangitis

Medium Vessel
1. PAN
2. ANCA associated
- Microscopic polyangitis
- Eosinophillic granulomatosis
- Granulomatosis with polyangitis

Large Vessel
1. Giant cell arteritis
2. Takayasu arteritis

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7
Q

What labratory investigations should be performed when vasculitis is suspected?

A

Biopsy:
1. for histopathology
2. Direct immunoflourescence

Bloods:
1. ANA
2. ANCA
3. HBV, HCV
4. HIV
5. strep (ASOT)
6. RF
7. CCP
8. C3 / C4
9. CH50, cryoglobulins
10. SPEP
11. Malignancy screen

To assess systemic involvement
1. Urinalysis
2. FBC, UEC, LFts
3. CXR
4. FOBT

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8
Q

A 24 year old presents with retiform purpura. You suspect a medium vessel vasculitis. How would you biopsy this lesion?

A

Incisional biopsy

OR

> 6mm punch biopsy

OR

Telescoping biopsy

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9
Q

What are the subtypes of occlusive vasculopathy? (5)

A

Coagulopathic
* Livedoid coagulopathy
* Antiphospholipid antibody syndrome
* Systemic hypercoagulability
* Warfarin induced skin necrosis

Embolic
* Endocarditis
* Cholestrol emboli
* Skin metastasis

Thrombotic
* Heparin induced skin necrosis
* Myeloproliferative disease
* Type I cryoglobulinaemia

Calcium Depletion
* Calciphylaxis
* Hypertensice ichaemic leg ulcer

Other
* Cocaine

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10
Q

What are the cutaneous manifestations of endocarditis?

A

Endocarditis
Petechiae
Oslers nodes (painful, eythematous lesions on the digits and toes)
Janeway lesions (painless haemorrhagic papules or macules on the palms and soles)
Splinter (linear, subungal) haemorrhages

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11
Q

What is the diagnostic criteria for calciphylaxis?

A

Must meet 3 clinical features OR 2 clinical features and classic histopathology findings.

Clinical features:
* On haemodialysis (or GFR <15ml/min)
* > 2 painful cutaneous ulcers with purpura
* Painful ulcers on the trunk, extremitis or penis with purpura

Classic histopathological finding:
* Ulceration and necrosis
* Calcificaiton of the tunica media and intima of small to medium arterioles in the dermis and subcutaneous fat
* concentric stenosis of the arterioles

Hayashi et al

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12
Q

What are the two (non infectious) categories of ulcer?

A

Inflammatory / vasculitic vs Vasooclusive

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13
Q

Management principles for ulcers

A
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14
Q

First-line pharmacological therapy for
pyoderma gangrenosum

A

JAAD CME 2024

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15
Q

Second line treatment in PG

A

methotrexate,
mycophenolate,
colchicine,
dapsone (topical or systemic),
azathioprine

biologics and small molecules
- etanercept,
- adalimumab,
- ustekinumab,
- guselkumab,
- risankizumab,
- tildrakizumab,
- anakinra,
- canakinumab,
- spesolimab,
- vilobelimab,
- apremilast,
- tofacitinib,
- upadicitinib
- baricitinib

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16
Q

Management of idiopathic cutaneous small vessel vasculitis

A

Rest
Elevation
Compression

Elimination or RX of triggers (medications, AI disease, infection)

17
Q

Describe important aspects of local ulcer care

A

(1) Tissue debridement:
* remove the slough or debris and necrotic tissue that may impede ulcer healing while preserving well-vascularized granulation tissue

(2) infection control:
* Systemic antimicrobials should be reserved for ulcer infection (not just colonization), associated soft-tissue infection, or osteomyelitis and should be tailored based on culture results

(3) moisture imbalance (dressing selection and
edema and perfusion management)
* Non-adherant dressing
* Compression

(4) epithelial edge advancement

18
Q

What are some of the epithelial edge advancement/Advanced and adjunctive therapies

A

reserved for chronic ulcers that do not improve by 50% after a minimum of 4 weeks of standard of care treatment

Topical timolol
- a b1/b2 antagonist
- proven promote re-epithelialization
- increase the rate of keratinocyte migration
- decreases the growth of Pseudomonas
aeruginosa

19
Q

Types of compression

20
Q

Types of debridement

A

autolytic debridement (with hydrogel or hydrocolloid dressings, concentrated surfactant gel such as Poloxamer 188 containing compounds which lead to the formation of a micelle matrix and allows wound debris to be loosened and washed away, honey),

enzymatic debridement (collagenase),
larval therapy,

mechanical debridement (pressurized wa-
ter jet, ultrasonic), and

surgical or sharp debridement.

22
Q

Benefits of debridement

A

Debridement promotes keratinocyte
migration and increased debridement frequency is
associated with faster healing.7

Tissue debridement
helps to address biofilms, which are structured communities of adherent microbial cells enclosed in
a polymeric matrix that are typically resistant to
penetration by antimicrobials,