Systemic Disease Derm Manifestations Flashcards

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1
Q

What is Systemic Lupus Erythematosus (SLE)?
Who is m/c affected?

A
  • Chronic inflammatory autoimmune condition that attacks multiple organ systems
  • F > M, AA > caucasian
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2
Q

S&S of SLE?

A
  • Malar rash (“butterfly” erythema)
  • Livedo reticularis (lacy)
  • Hives
  • Photosensitivity
  • Oral ulcers
  • Hairloss
  • Raynauds
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3
Q

What are the forms of Cutaneous Lupus Erythematous?

A

Acute: butterfly rash, morbilliform eruption, erythema & edema of hands sparing the joints

Subacute: annular scaly “psoriasiform” patches in photodistribution

Chronic
Discoid: erythematous/violaceous scaly plaques with follicular plugging –> scarring & atrophy

Tumid: juicy papules/plaques, no scarring

Panniculitis (ex. Erythema Nodosum): involves SQ tissue, painiful nodules

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4
Q

Who is m/c affected by Discoid Lupus Erythematosus?
Where is it m/c located?

A
  • Young-middle aged women
  • Face, scalp, ears (neck up)
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5
Q

What skin manifestations do you see with Discoid Lupus Erythematosus?

A
  • Well circummscribed erythematous scaly plaques (ITCHY)
  • Follicular plugging (little scale w/i follicle)
  • Telangiectasias
  • Atrophy
  • Dyspigmmentation
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6
Q

How is Discoid Lupus Erythematosus dx?

A

Skin Biopsy +/- DIF

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7
Q

How is Discoid Lupus Erythematosus treated?

A
  • Topical/IL/Oral steroids
  • Cyclosporine
  • Hydroxychloroquine
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8
Q

What is Erythema Nodosum?
What does it look like?
Where is it m/c located?
Who is m/c affected?

A
  • M/C inflammatory panniculitis, Delayed hypersensitivity reaction
  • Deep tender dusky erythematous nodules
  • M/C on Lower extremities (shins), Bilateral/symmetrical
  • F > M, 20-40 y/o
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9
Q

What are causes of Erythema Nodosum?
What’s S&S is it associated with?

A
  • Causes: Idiopathic, Infections (Strep, TB), Drugs, Sarcoid, IBD
  • Associations: Malaise, Leg edema, Arthralgia, Fever, H/A, Conjunctivitis, GI issues
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10
Q

How is Erythema Nodosum diagnosed?

A

Clinically, Biopsy (deep fat)

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11
Q

How is Erythema Nodosum treated?

A
  • Bed rest
  • Salicylates
  • NSAIDs
  • Potassium Iodide
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12
Q

What is Dermatomyositis?

A

Idiopathic inflammatory condition with characteristic myositis & cutaneous findings

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13
Q

What are the S&S of Dermatomyositis?

A

Cutaneous:
- Erythema/edema of face & eyelids
- Scaly patches on extensor surfaces of extremities
- Dilated vessels at proximal nail folds
- Heliotrope rash: pink/violet patches on eyelids, erythema around eyes
- Gottrons papules: flat-topped polygonal papule over knuckles
- Shawl sign
- V-sign: violaceous/poikiloderma upper chest
- Mottled hyper/hypopigmentation

Systemic:
- Intermittent fever
- Malaise
- Anorexia
- Arthralgias
- Weight loss
- Dysphagia
- Proximal muscle weakness

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14
Q

How is Dermatomyositis definitively diagnosed?

A

Muscle Biopsy or Skin Biopsy

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15
Q

What labs and imaging are ordered for Dermatomyositis?

A

Labs:
- Creatinine Kinase
- Aldolase
- LDH
- Transaminases
- ANA (positive in 60-80%)

Imaging:
- EMG
- MRI
- Xray (Barium Swallow)

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16
Q

How is Dermatomyositis treated?

A
  • Sun avoidance
  • Topical steroids
  • Plaquenil
  • Oral steroids like Prednisone, MTX, etc.
17
Q

What is Necrobiosis Lipoidica Diabeticorum?
Where is it m/c located?
Who is m/c affected?

A
  • Skin condition associated with Diabetes and glucose intolerance, has to do with collagen degeneration and dermal inflammation
  • M/C on shins
  • Mostly women, 34 y/o
18
Q

What does Necrobiosis Lipoidica Diabeticorum look like?
Other S&S?

A
  • Yellow, waxy firm plaques
  • Decreased sensation to pin prick/fine touch
  • Hypohidrosis
  • Partial alopecia
19
Q

How is Necrobiosis Lipoidica Diabeticorum diagnosed?

A

Punch Biopsy (from palpable perimeter)

20
Q

How is Necrobiosis Lipoidica Diabeticorum treated?

A

ONLY HALTS PROGRESSION
- Control DM
- ILTAC-in advancing border (avoid yellow center)
- Topical/Oral Steroids