1.2 Pathology of Skin (pt 2) Flashcards

1
Q

how does seborrheic dermatitis present microscopically

A

spongiotic dermatits & acanthosis w/ parakeratotic mounds around the hair follicles (“follicular lipping”) & mixed inflam population

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2
Q

what is pemphigus vulgaris

A

most common

-mucosa & skin (esp scalp); may present in oral ulcers

lesion = superficial vesicle & bullae rupture easily = suprabasalar blister - part of epidermis (including stratum corneum)

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3
Q

what is hereditary angioneurotic edema?

A

inherited deficiency of C1 inhibitor –> excess activation of early components of complement & produce vasoactive mediators

worry about this when angioedema present (which is related to utricaria but has edema in deeper dermine & subQ fat)

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4
Q

what is an example of disorders of epidermal maturation

A

ichthyosis

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5
Q

What is erythema multiforme associated with?

(=the self-limited hypersensitivity rxn)

A
  1. infxns (viral, bacterial and fungal) *HSV & mycoplasma & histoplasma & coccidiomycosis*
  2. drugs (sulfa, penicillin, barbiturates, salicylates, antimalarial, hydantoins)
  3. cancer
  4. collagen vascular dz (SLE, dermatomytosis & polyarteritis nodosa)
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6
Q

what is epidermolysis bullosa

A

=non-inflam

= group of disorders due to inherited defects in structural protein that provide mechanical stability (keratin)

commonly: form blistes at sides of pressure, rubbing or trauma or at/soon after birth

so subtle that electron microscopy may be required to differentiate btn types

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7
Q

What are examples of panniculitis

(define panniculitis)

A

erythema nodosum

erythema induratum

=inflam of subQ layer of fat (deep & nodular)

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8
Q

What is seborrheic dermatitis? what is it correlated w/?

A

= chronic inflam, more common than psoriasis

involves regions w/ high density of sebaceous glands (scalp, forehead, external auditory canal, retroauricular area, nasolabial folds and presternal areas)

BUT** rmr **NOT a dz of glands it self

correlations = HIV w/ low CD4 count & parkinsons

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9
Q

what are examples of epidermal appendages

A

acne vulgaris

rosacea

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10
Q

describe ichthyosis & its morphology

A

inherited disorder - seen at or soon after birth

=disorder of epidermal maturation ==> hyperkeratosis –> fishlike scales

morphology: build up of compacted stratum cornem ; defective desquamation –> retention of abnormal formed scale

some variants = paraneoplastic of lymphoid or visceral malignancy (esp GI tract)

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11
Q

how long do acute inflam lesions last?

what are they characterized by?

A

days - weeks

=characterize by inflam inflitrates (lymphocytes, macrophages), edema, degree of epidermal, vascular or subcutaneous injury

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12
Q

what are characterisics of the bacteria is causing proprionibacterium acne

what has it been recently associated with?

A

“Acutibacterium” - proprionibacterium (gram +) - prefer anaerobic

= actinobacteria

associated w/ chronic blepharitis & endophthalmitis (after intraocular surgery) & prosthetic related infxn, & chronic nerve root inflam

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13
Q

What is pemphigus foliaceus

A

blister found in superficial epidermis at level of stratum granulosum

subcorneal blister - stratum corneum forms roof of bulla

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14
Q

what is verruca vulgaris?

what is the pathogenesis/morphology

A

common warts (esp kids)

pathogenesis: HPV
morphology: verrucous/papillomatous epidermal hyperplasia ; koilocytosis (cytoplasmic alterations) = (pic C)

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15
Q

treatment with _____ & ____ have shown efficacy for psoriaris w/ auspitz sign

A

anti-TNF & anti- IL 17

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16
Q

how does erythema multiforme present?

A

macules, papules, vesicles & bullae

cutaneous & mucucutaneous “target” lesion - face & extremities

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17
Q

what is lichen planus?

How does it present (acute & chronic)

A

6 P’s: Pruritis, Purple, Polygonal, Planar, Plaque, Papules

disorder of the skin & mucosa

=self limited (resolve w/i 1-2 yrs) - resolution will leave residuum of post-inflam hyperpigmentation & oral lesions may persist for years

SCC occur in chronic mucosal & paramucosal lesions

Koebner phenomenon (like psoriasis)

Wickham striae: white dots/lines that highlight the papule

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18
Q

How does dematitis herpetiformis present?

whats the pathogenesis/morphology behind it?

A

= urticaria & grouped vesicles; plaques and vesicles are extremely pruritic

M>F, 30s-40s

pathogenesis: *association w/ intestinal celiac dz* - responds to gluten free diet

Ab cross react w/ reticulin –> subepidermal blister

morphology: IgA granular deposits - localize in the tips of dermal papillae

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19
Q

what is the difference in action of mast cells in acute vs chronic response

A

acute: IgE Ab bind to Fc receptor –> cell degranulate and release mediators (histamine and prostoglandins)
chronic: secrete cytokines and promote inflam rxn

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20
Q

What are examples of chronic inflam dermatoses

A

psoriasis

seborrheic dermatitis

lechin planus

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21
Q

what are causes for acne

*rmr: Whitehead = open & blackhead = closed*

A

hormonal fluctuation, androgens

obstructive effects

chronic inflam

proprionibacterium (reason why antibiotics can be use to treat acne!)

22
Q

What are the different levels w/i the skin that blisters can develop

A
  1. Subcorneal: stratum corneum from roof of bulla (under stratum corneum) pemphigus foliaceus
  2. Suprabasal: portion of epidermis, including stratum corneum, form roof (right above basalar layer) pemphigus vulgaris
  3. Subepidermal : entire epidermis and dermis separate bullous pephigoid
23
Q

what are examples of derm infections

A

verracae

molluscum contagiosum

impetigo

superficial fungal infxn

24
Q

what are examples of acute inflam dermatoses

A

urticaria

acute eczematous dermatitis

erythema multiform

25
Q

what is the pathogenesis and morphology for acute eczematous dermatitis?

A

pathogenesis: Type IV hypersensitivity
morphology: red, papulovesicular (blister), oozing –> if persistent - reactive acanthosis and hyperkeratosis make raised plaques

(lesions are prone to bacterial superinfxn –> yellow crust (impetiginization))

=characterized by “epidermal spongiosis” -edema in intercel space - prominent seperation btn keratinocytes (esp stratus spinosum)

26
Q

What type of panniculitis tends to affect teen & menopausal women

describe the disorder

A

erythema induratum

-possible primary vasculitis of deep vessels supplying fat lobules of subQ skin

erythematous nodules –> ulcerate

27
Q

what is acantholysis

A

splaying apart keratinocytes due to spongiosis

28
Q

what derm disorder is associated w/ increased/abnormal endogenous anti-microbial proteins & activation certain mediates like toll-like receptors?

A

Rosacea

(i. e catheliciden peptide)
- face (cheek, nasolabial fold)

chronic inflam

Spectrum = persistent erythema <–> pustules <–> development of rhinophyma (ENLARGED NOSE)

29
Q

What is the morphology of Lichen Planus?

A

wickham stria

= pink-purple, polygonal papule w/ white lacelike pattern

  • has bandlike infiltrate of lymphocytes at dermoepidermal jxn, hyperkeratosis and pointed rete (sawtooth)
30
Q

what is psoriasis and what other conditions is it associated w/

A

= chronic inflam dermatosis that appears to have autimmune basis (see in all ages)

-associated w/

  1. arthritis (15%)- may be mild or produce deformities resembling RA (one side or symmetric)
  2. myopathy
  3. enteropathy
  4. AIDS
31
Q

What is the pathogenesis & morphology for psoriasis

A

pathogenesis: sensitized CD4, Th17 and activated CD8; driven by Th1 & Th17 (IL 12, IL 17, INF-gamma & TNF) ; 2/3 pt = HLA-C gene

Koebner phenomenon: areas w/ trauma have psoriatic lesions bc motion for local inflam which becomes self-perpetuating

morphology:

  1. nail changes
  2. stratum granulosum thinned/absent
  3. biopsy show: change in papilary dermis, acanthosis, scaling, microabsess in stratum corneum
  4. Auspitz Sign - dilated vessels of underlying dermal papillae - multiple, minue and bleeding point
32
Q

What is pemphigus vegetans

A

large, moist, wart-like vegetating plaque studded w/ pustules

cells immediately above basal layer

overlying epidermal hyperplasia

33
Q

what are the 5 types of pemphigus

A

vulgaris

vegetans

foliaceous

erythematosus

paraneoplastic

34
Q

What is the pathogenesis and morphology of impetigo

A

= common superficial bacterial infxn (usually due to Staph aureus)

pathogenesis: innate immune response –> epidermal injury –> local serous exudate & form scab

& blister formation = bacterial production that cleaves desmoglein 1 (responsible for cell-cell adhesion in upper most epidermal layers)

morphology: erythematous macules that progress to small pustules –> to shallow erosions covered w/ drying serum as pustules (honey colored crust)

accumulation of neutrophils beneath stratum corneum

35
Q

What is bullous pemphigoid

A

subepidermal, nonacantholytic blister

elderly pts

-inner thigh, flexor surfaces - forearm, axillae, groin and lower abdomen

oral lesion (10-15%)

possible utricarial plaques w/ severe pruritus

auto-ab IgG - bind to proteins required for adherence of basal keratinocytes to BM (hemidesmosomes)

36
Q

What are toxic epidermal necrolysis & steven johnson syndrome

A

=severe epidermolytic adverse cutaneous drug rxns (skin & mucous membrane)

  • rare; medical emergencies!

=mucocutaneous tenderness & hemorrhagic erosions, erythema and more/less severe epidermal detachment - presenting as blisters & ares of denuded skins

differ by extend of skin detachment

37
Q

what is pemphigus erythematosus

A

localized

may have selective malar presentation like SLE

38
Q

what are characterisitics and examples of superficial fungal infxns

A

confined in stratum corneum

caused by dermatophytes from soil or animal

= bright pink/red w/ PAS & are found in anucleated cornified layers of lesional skin, hair or nails

39
Q

What is Molluscum Contagiousm

A
  • self limited viral skin dz (children & young adults)
    morphology: umbilicated pink papules; molluscum bodies - large ellipsoid, homogenous, cytoplasmic inclusions in cells of stratum granulosum & corneum
40
Q

what are the subdivisions of acute aczematous dermatitis?

A
  1. allergic contact
  2. atropic
  3. drug-related
  4. photoeczematous
  5. primary irritant
41
Q

What is the NODOSUM mneumonic for erythemal nodosum

A

NO cause found in 60% cases = idopathic

Drugs (sulfa, antibiotics, etc)

Oral contraceptives

Sarcoidosis or Lofgren’s syndrome

UC, crohns, bechets

Micro: (infxns - TB, EBV, HSV, camplobacter, syphilis, etc)

= nodular & painful = septal panniculitis

42
Q

what is paraneoplastic pemphigus

A

associated w/ malignancies (most common NHL)

Auto-Ab that recognize desmogleins or other proteins of intercellular adhesion

43
Q

what is the immune mechanism, histopathologic lesions of type I (immediate) hypersensitivity

(when do these rxns occur?)

A

=make IgE Ab -> release vasoactive amines from mast cells & later recruit inflam cells

histopath lesions: vascular dilation, edema, Sm M contraction, mucous production, tissue injury & inflam

(anaphylaxis, allergies, bronchial asthma)

44
Q

what is pemphigus caused by

A

IgG auto-Abs against desmogleins- result in dissolution of intercellular attachment w/i epidermis & mucosal epithelium

5 types

45
Q

What is Weber-Christian Dz

A

relapsing febrile nodular panniculitis

46
Q

how does psoriasis present?

A

on elbows, knees, scalp, lumbosacral areas, intergluteal cleft & glans penis

=pink to salmon colored plaque covered by loosely adherent silver-white scale

possible nail changes- yellow-brown discoloration w/ pitting, dimpling, separation of nail plate (onycholysis) , thickening, crumbling

47
Q

what are examples of blistering (bullous) dzs

A

inflam

  1. pemphigus
  2. bullous pemphigoid
  3. dermatitis herpetiforms

Noninflam

  • epidermolysis bullous and porphyria
48
Q

What are porphyrias

A

= noninflam

=group of uncommon inborn/acquired distrubances of porphyrin metabolism

*porphyrin - pigments in Hb, myoglobin and cytochromes

bone and skin involvement - urticaria & vesicles associated w/ scarring (worse w/ sunlight)

49
Q

if a pt presents w/ firm edematous plaques that last only a few hrs..

what do they have?

describe the morphology

A

Utricaria (wheals - hives)

firm edematous plaque resulting from infiltration of dermis w/ fluid

type I hypersensitivity ==> localized mast cell degranulation –> dermal microvascular hyperpermeability

compare w/ angioedema - which is edema of deeper dermis & subQ fat

morphology: sparse mononuclear infiltrate & occasional dermal eosinophils

50
Q

what are chronic inflam lesions characterized as

A

month- years

= epidermal changes (atrophy/hyperplasia) &/or dermal fibrosis