11- Cutaneous Reaction Patterns Flashcards

1
Q

Doxycyline is known to cause _____ and _____ reactions.

A

Photosensitivity and sunburn

This is dose-dependent and predictable.

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2
Q

In general, allergy testing or other diagnostic tests are not helpful in pinpointing the specific culptrit when a cutaneous drug eruption is suspected. What is the exception to this?

A

Exception is the skin-prick testing to detect IgE-mediated penicillin reaction.s

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3
Q

What is the appearance of urticaria? How long do they last?

A

Aka hives - pink edematous papules and plaques that occur on the skin.

Lesions migrate and individual lesions last less than 25 hours, though the reaction as a whole may last longer.

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4
Q

What are three forms of anaphylaxis? What are they caused by?

A

Urticaria, angioedema, and aphaphylactic shock.

IgE-mediated immediate hypersensitivity.

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5
Q

What isthe most commonly identified cause of acute urticaria?

A

Upper respiraoty infection (but most are idiopathic); Drugs cause 10%

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6
Q

How would you treat urticaria?

A

A non-sedating antihistamine such as loratidine, cetirizine, and fexofenadine - combined with sedating class H1 antihistamines (diphenhydramine, hydroxyzine).

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7
Q

What is the most common cutaneous drug eruption? What type of reaction is this?

A

Exanthematous drug eruptions - aka morbiliform drug rashes

Type 4 (delayed) hypersensitivity

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8
Q

What do Exanthematous drug eruption lesions look like?

A

Monomorphic (invidiual lesions look like each other) macules and thin papules that start on the face and trunk and spread to extremities.

Usually pruritis and a low grade fever may occur.

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9
Q

What is the onset of exanthematous drug eruption? How do you treat it?

A

Usually 2-14 days after drug initiation, sometimes starting even after discontinuation.

They typically resolve on their own over 1-2 weeks, even with continuation of the drug. Treatment is supportive for the pruritis (topical corticosteroids and oral antihis.)

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10
Q

What is DRESS? What are associated symtpoms?

A

Drug reaction with eosinophilia and systemic symptoms.

Resembles exanthematous drug eruptions, but is commonly associated with fever.

Facial edema, enlarged noes, and arthralgias may also occur.

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11
Q

What is characteristic of DRESS but isn’t always present? What is the most common site of involvement in DRESS?

A

Eosinophilia characteristic but not always present.

Most common site: liver, seen with incresed hepatic enzymes.

Also myocarditis, pneumonitis, nephritis, thyroiditis, and brain involvement seen.

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12
Q

DRESS is fatal in ____% of patients. What is required to treat it?

A

Fatal in 10%

Systemic corticosteroids are required to treat most cases

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13
Q

What disease is characterized by targetoid lesions seen on acral sites?

A

Erythema multiforme - historically through to represent a spectrum of diseases with the same disease process as SJS and TEN but is now through to be a distinct disorder.

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14
Q

Describe the lesions seen on someone with erythema multiforme? How long do they last?

A

Target lesions with 3 or more color zones and dusky red or purple center.

They arise abruptly on acral areas and last up to 2 weeks.

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15
Q

What causes erythema multiforme?

A

Infectious triggers (most commonly HSV) make up 90% of cases

Drugs make up <10% of reactions

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16
Q

How would you treat erythema multiforme?

A

Systematic treatment for pain or pruritis

Severe disease: systemic corticosteroids may be needed

17
Q

What are Stevens-Johnson syndrome (SJS), and toxic epidermal necrolysis (TEN), and SJS/TEN? What precedes them?

A

Disorders that are severe and life-threatening and represent the same disease continuum.

Usually preceded by fever, malaise, and upper resp. symptoms before the onset of cutaneous lesions.

18
Q

What cutaneous lesions are seen with SJS/TEN?

A

Painful red patches that evolve rapidly to bullae and areas of necrosis.

19
Q

What are the differences between SJS, TEN, and SJS/TEN overlap? What areas are involved?

A

SJS: epidermal detachment <10% of body SA

SJS/TEN: 10-30% body SA with epidermal detachment

TEN: >30% body SA

Any mucosal surface can be involved.

20
Q

What drugs are most commonly invovled in SJS, TEN, and SJS/TEN?

A

Allopurinol, NSAIDs, sulfa drugs, anticonvulsants (lamotrigine, carbmazepine, phenobarbital, and phenytoin), and antibiotics.

21
Q

What is the mortality rate for severe cases of TEN? What is death usually caused by?

A

35%

Sepsis

22
Q

How would you treat SJS, TEN, SJS/TEN?

A

Prompt discontinuation of the causal drug is key.

Supportive multidisciplinary care.

23
Q

What is vasculitis? How is it classified?

A

Inflammation and destruction of blood vessels, either arteries or veins.

Group of disorders with a range of clinical presentations. Can be classified based on size of affected vessel.

24
Q

Most cutaneous vasculitis is ____ vessel vasculitis with the inflammation centered around _______ and _______ in the dermis.

A

Most cutaneous vasculitis is small vessel vasculitis with the inflammation centered around arterioles and venules in the dermis.

25
Q

What are two diseases associated with vasculitis of large arteries?

A

Takayasu arteritis

Giant Cell arteritis

26
Q

What are two diseases associated with vasculitis of medium sized arteries?

A

Polyarteritis nodosa

Kawasaki disease

27
Q

What are three diseases associated with vasculitis of small vessels and medium arteries?

A

Granulomatous vasculitis

Churg-Strauss syndrome

Microscopic polyaniitis

28
Q

What are two diseases associated with vasculitis of small vessels?

A

Cutaneous leukocytoclastic vasculitis

Henoch-schonlein purpura

29
Q

What is leukocytoclastic vasculitis (LCV)?

A

Histologic diagnosis associated with multipel clinical presentations.

Term given to small vessel vasculitis of the skin when PMNs are predominant inflammatory cell on biopsy.

30
Q

What is the most common cause of leukocytoclastic vasculitis? What are some other causes?

A

About 50% are idiopathic

Common causes: infections (URI, group A strep, HepB and HepC, HIV) and drug hypersensitivity (antibiotics)

31
Q

What cutaneous findings are seen with leukocytoclastic vasculitis?

A

Palpable purpura, usually more common on the legs.

Urticarial lesions may be seen but unlike true uticaria, these are fixed for >24 hrs.

Other possibilities: nodules, ulceration, livedo reticularis (purple, lacy, net-like pattern).

32
Q

What is henoch-schonlein purpura (HSP)? What is seen on biopsy?

A

Small vessel vasculitis that usually affects children.

A leukocytoclastic vasculitis is seen, but IgA immune complexes are a more specific finding when immunofluoresence is performed.

33
Q

What commonly triggers henoch-schonlein purpura?

A

Infections, particularly group A strep and other URIs.

34
Q

What do lesions from henoch-schlonlein purpura look like?

A

Main findings: palpable purpura on skin, especially on the buttocks and lower extremeties.

Also possible: arthritis, abdominal pain, GI bleeding, and nephritis.

35
Q

How should you treat henoch-schonlein purpura?

A

It’s self-limited and resolves over the course of 2-4 weeks.