Papulosquamous and Inflammatory Dermatoses Flashcards

(77 cards)

1
Q

KERATOSIS PILARIS

Etiology/Epidemiology

A
  • disorder of keratinization of hair follicles of the skin
  • exact etiology unclear, but some genetic link
  • sex: F > M
  • may appear at any age; affect 50-80% of all adolescents and 40% of adults
  • associated with other dry skin conditions: ichthyosis vulgaris, xerosis, atopic dermatitis
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2
Q

KERATOSIS PILARIS

Clinical Features

A
  • small (1-2mm) rough folliculocentric keratotic papules, sometimes pustules
  • erythematous papules w/ light red halo
  • distribution: posterolateral upper arms, anterior of thighs, buttocks, face, can affect any area, spares palms and soles
  • asymptomatic (most) to mild pruritus
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3
Q

KERATOSIS PILARIS

  1. Diagnosis
  2. Differential diagnosis
A
  1. clinical appearance

2. miliaria rubra, acne/folliculitis, drug eruption

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4
Q

KERATOSIS PILARIS

Treatment

A
  • mild cleansers
  • emollients
  • keratolytic: 12% ammonium lactate, urea cream, topical retinoids (RetinA, tazorac)
  • topical steroids
  • patient education: reassure b/c not contagious and won’t cause problems
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5
Q

XEROSIS

A
  • dry skin
  • important feature of the atopic state
  • affects all ages
  • decreased barrier function of skin
  • aggravating factors: winter, low humidity, hot water, harsh products (soaps, fragranced lotions)
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6
Q

XEROSIS

Clinical appearance

A
  • erythema, horizontal linear splits (cracks)
  • most common on extensor surfaces but not limited to these areas
  • increased sensitivity, easily irritated
  • may itch or burn
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7
Q

XEROSIS

Diagnosis

A

-clinical appearance

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8
Q

XEROSIS

Treatment

A
  • avoid triggers: 100% cotton, mild detergent, no bleach or fabric softener, use mild or no soap, clip nails to decrease abrasion, avoid frequent washing and drying
  • topical therapies: wet dressings, short cool showers, emollients immediately after bathing, frequent soaking and greasing, oils > ointments > creams > lotions
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9
Q

ICHTHYOSIS VULGARIS

Etiology

A
  • disorder of keratinization characterized by the development of dry, rectangular scales
  • onset at birth or later in life??
  • various forms: inherited (95% of cases) and acquired
  • autosomal dominant
  • sex M = F
  • often seen in AD patients: keratosis pilaris, hyperlinear palmar creases, atopy
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10
Q

ICHTHYOSIS VULGARIS

Clinical features

A
  • fine, white, adherent, polygonal scale with central tacking
  • extensor extremities: lower > upper
  • flexural folds and diaper = spared
  • improves as adult
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11
Q

ICHTHYOSIS VULGARIS

  1. Diagnosis
  2. Treatment
A
  1. clinical appearance
  2. emollients; lactic acid, urea, or alpha-hydroxy acids for severe scaling; patient education about avoiding drying environments; humidification
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12
Q

PSORIASIS

A
  • common, chronic, inflammatory, papulosquamous disease that affects the skin, nails and joints
  • several distinct clinical forms
  • severity and extent of disease varies widely
  • once expressed, generally follows relentless, waxing and waning course
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13
Q

PSORIASIS

Pathophysiology

A
  • proliferation of the outer layers of skin due to abnormal T lymphocyte and dendritic cell function/communication
  • reactive increase in growth of epidermal and vascular cells
  • 8 fold shortening of epidermal cell cycle (build up of cells)
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14
Q

PSORIASIS

Epidemiology

A
  • 1-3% of the population
  • inherited genetic factors and known environmental triggers
  • age: onset any age; peaks in 20s and 50s
  • heredity: 1/3 have positive family history
  • sex: M = F
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15
Q

PSORIASIS

Triggers/Predisposing conditions

A
  • trauma (Koebner phenomenon)
  • infection (strep, HIV, candida, dental)
  • stress/winter season
  • smoking/alcohol
  • drugs: beta blockers, lithium, systemic steroids, antimalarials, NSAIDs, ACE inhibitors
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16
Q

PSORIASIS

Clinical features

A
  • chronic plaque psoriasis: most common form
  • red, scaly, round to oval plaques
  • symmetrical, sharply marginated
  • loosely adherent silvery white scale
  • extensor surfaces: predominantly elbows, knees, scalp; also gluteal cleft, umbilicus, penis; spares the palms, soles and face
  • degree of pruritus varies by individual and type
  • Auspitz sign: pinpoint bleeding when scale removed
  • Koebner phenomenon: psoriasis develops at site of trauma
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17
Q

Types of Psoriasis

A
  • chronic plaque
  • guttate (acute eruptive)
  • pustular
  • erythrodermic
  • inverse psoriasis (intertriginous)
  • light sensitive
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18
Q

GUTTATE PSORIASIS

A
  • gutta = “drop” in Latin
  • > 30% of first episodes are before 20 y.o
  • usually preceded 1-2 weeks by strep pharyngitis or viral infection
  • resolves spontaneously in weeks to months
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19
Q

GUTTATE PSORIASIS

Clinical features

A
  • small, scaly papules SUDDENLY appear
  • trunk and extremities
  • uniform lesions
  • spares palms and soles
  • may or may not have pruritus
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20
Q

PUSTULAR PSORIASIS

A
  • localized: small sterile pustules on a red base on palms and soles
  • generalized (von Zumbusch’s syndrome): widespread sterile pustules can coalesce into large areas of pus; life threatening
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21
Q

INVERSE PSORIASIS

A
  • uncommon
  • smooth, red and sharply defined plaques
  • found in flexural or intertriginous areas (groin, axilla, under breasts)
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22
Q

ERYTHRODERMIC PSORIASIS

A
  • entire skin surface is involved
  • generalized erythema and scaling
  • can be very severe
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23
Q

Conditions Associated with Psoriasis

A
  • arthritis: affects 5-8% of psoriasis patients; with or w/o cutaneous psoriasis; rheumatoid factor negative; most common is asymmetric, oligoarticular form (70% of psoriatic arthritis)
  • IBS, cardiovascular disease, depression
  • nail disease: 1/3 of patients; pitting subungual debris; oil drop sign; nail dystrophy and onycholysis
  • scalp: dense scale covering part or all of scalp; can be difficult to determine seborrheic dermatitis
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24
Q

PSORIASIS

Diagnosis

A
  • clinical appearance
  • biopsy (punch)
  • labs: positive anti streptolysin O titer/throat culture (guttate); KOH to rule out candida; HIV titer; autoimmune screens (ANA, ESR, RF)
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25
GUTTATE PSORIASIS Differential diagnosis
- chronic plaque: seborrheic dermatitis, nummular eczema, tinea corporis, drug eruption - guttate: pityriasis rosea, secondary syphilis, drug eruption - inverse: candida, contact dermatitis, bacterial infection
26
PSORIASIS Treatment
- topical steroids/intralesional - tar preparations - salicylic acid (scalp) - vitamin D analogues - retinoid creams - anthralin - phototherapy UVB - systemic: methotrexate, cyclosporine, acitretin, PUVA, biologics - patient education
27
PITYRIASIS ROSEA
- acute, self-limiting skin eruption - etiology unclear, but thought to be viral in origin - sex: M = F
28
PITYRIASIS ROSEA Predisposing factors
- age: >75% between 10-35 y.o.; rare in young and old - seasonal: more common in cooler months (spring/fall) - clustered in families/close contacts - higher incidence in immunocompromised
29
PITYRIASIS ROSEA Clinical features
- mild URI prodrome - primary lesion: Herald patch - a solitary lesion, usually annular, 2-6 cm, round to oval, most common on trunk and neck but can occur anywhere - secondary lesions: 1-2 wks after 1ary; generalized eruption on trunk and proximal limbs; salmon pink; 0.5-1.5 cm macules or patches; Christmas tree distribution; collarette scale (inward facing cigarette paper-like appearance) - symmetrical eruption, but spares palms/soles - atypical presentations: small papules common in young and pregnancy
30
PITYRIASIS ROSEA 1. Diagnosis 2. Differential dx
1. clinical appearance; biopsy not typically required 2. guttate psoriasis, viral exanthems (kids), tinea corporis (ring worm), nummular eczema, lichen planus, drug eruptions, seborrheic dermatitis, secondary syphilis
31
PITYRIASIS ROSEA Treatment
- no treatment (self-limiting) - emollients for scale - topical corticosteroids (class V) for itching - PO antihistamines, antipruritic lotions - NO topical lidocains or benadryl! - UVB phototherapy/direct sun
32
LICHEN PLANUS Etiology/Epidemiology
- inflammatory cutaneous and mucous membrane reaction pattern - unknown etiology
33
LICHEN PLANUS Predisposing factors
- sex: F > M - age: may occur at any age; adults most common 30-60; rare in kids under 5 - family history: 10% positive FHx - may be associated w/ chronic active hep C - lichen planus-like eurptions due to medications, chemical exposure, post bone marrow transplant
34
LICHEN PLANUS Clinical features (location and the 5 Ps)
- location: skin, mucous membranes, genitalia, nails, scalp; flexor surfaces of wrist, forearms, legs just above ankles - pruritic - planar (flat top) - polyangular - purple (violaceous) - papules
35
LICHEN PLANUS Clinical features (size, grouping, special/unique characteristics)
- 1 mm - 1 cm - random clusters, discrete, linear, annular, or diffusely papular (guttate) - Koebner phenomenon: lesion in response to injury/scratch - Wickham striae: white, lacy reticular pattern of criss crossed lines - new lesions appear pink/white then become purple with waxy luster - heals w/ post inflammatory hyperpigmentation
36
Papular Lichen Planus
- most common form - found on wrist, forearm, ankles and low back typically - often chronic - average 4 years
37
Hypertrophic Lichen Planus
- 2nd most common - can be anywhere, but most common on shins and ankles - become confluent, rough red-brown thick - may have severe itching and last for avg 8 years - can develop vesicle/bullae
38
Follicular Lichen Planus
- localized to hair follicles - may occur with papular form - causes hair loss (can be permanent from scarring)
39
Mucosal Lichen Planus
- mucosal membrane (oral, vulva, glans penis) - oral: can occur w/o cutaneous lesions - F>M, mean age onset 60 y.o - seen in greater than 50% with cutaneous lesions - most common form is non-erosive with white lacy pattern on buccal mucosa - erosive form more severe and painful; 0.5-3% develop into SCC
40
Lichen Planus Nail Disease
- longitudinal grooving, ridging, splitting, thinning and red streaks/dots, pterygium - tenting or pup tent = elevation of nail plate - 25% of pts with nail LP have LP at other sites before or after nail disease is noted - most common age 50s-60s
41
LICHEN PLANUS 1. Diagnosis 2. Differential dx
1. clinical appearance; biopsy for confirmation if needed; AST/ALT/alk phos (liver fx tests), HIV, Hep C tests 2. cutaneous: syphilis, lichen simplex chronicus, guttate vs plaque psoriasis mucosal: candida, SCC, leukoplakia
42
LICHEN PLANUS Treatment
- refer to derm: generalized or mucosal disease, scarring alopecia, and refractory cases - topical corticosteroids: initial Tx of localized disease - intralesional corticosteroids sometimes used for hypertrophic lesions - anti-histamines for pruritus - topical corticosteroids in orabase for oral lesions
43
GRANULOMA ANNULARE
- benign, inflammatory/reactive dermatosis; self-limited - unknown pathophysiology - several clinical variants; localized GA is most common
44
GRANULOMA ANNULARE Predisposing conditions
- sex: 2F:M - age: localized GA most common in kids and adults <10 or adults 30-60 - seasonal: worse in summer, better in winter
45
GRANULOMA ANNULARE Clinical features
- primary lesion: firm, 1-2 mm, skin colored to erythematous papules; slowly progressing; grouped lesion expand to arcuate or annular plaques; central depression; smooth and non-scaling - dorsal surface of hands/feet/fingers; extensor of arms and legs; rare on face, scalp, genitals - asymptomatic or mild pruritus - duration: variable; weeks to decades; spontaneous involution w/in 2 years in 50%
46
GRANULOMA ANNULARE Hypothesized Associations
- diabetes - TB - insect bites/trauma - sun exposure - thyroid disease - viral infections: HIV, Epstein Barr, herpes zoster
47
GRANULOMA ANNULARE 1. Diagnosis 2. Differential dx
1. clinical appearance, maybe a biopsy, KOH (- to r/o ringworm) 2. tinea, annular lichen planus, basal cell carcinoma, erythema migrans (Lyme), sarcoidosis, nummular eczema
48
GRANULOMA ANNULARE Treatment
- asymptomatic localized lesion can be left untreated - topical corticosteroids not very effective (class I or II under occlusion, use in intervals) - intralesional Kenalog at the elevated border - cryotherapy - other generalized variants may need systemic treatment
49
URTICARIA
- reactive immunologic/inflammatory process - also referred to as hives or wheals - prevalence: may occur at any age; up to 20% of pop will have one episode; may be more common in atopic pts - cause undetermined in most causes - acute or chronic
50
URTICARIA Pathophysiology
- mast cell releases histamine in response to immunologic, non-immunologic, physical and chemical stimuli - H1 receptors: triple response of Lewis (vasodilation-ereythema, axon reflex-pruritus, and wheal) - H2 receptors: vasodilation, increased gastric secretion
51
URTICARIA Acute vs. Chronic
- acute: less than 6 weeks; majority of cases; lasts few hours to few weeks; more common in kids and young adults; cause usually undetermined - chronic: more common in young adults and middle age women; cause determined in 5-20% of cases
52
URTICARIA Clinical features
- raised, red, transitory area of edema - various sizes and shapes: papules, plaques, annular, arcuate, polycyclic - newest lesions are reddest - no scale - pruritus varies in severity - sudden onset; each lesion last <24 hours - occur on any skin surface
53
URTICARIA Classifications
- ordinary: 4-36 hours - contact: 1-2 hrs, biological or chemical - urticarial vasculitis: 1-7 days - physical: 30 min-6 hrs; aquagenic, cholinergic (stress), cold, delayed pressure, dermatographism, exercise induced, localized heat, solar, vibratory
54
Dermatographism
- "skin writing" - minor trauma/scratch = hive - lasts < 30 minutes
55
URTICARIA Common causes
- recent infection: viral, bacterial - medications: ACE inhibitors, aspirin, NSAIDs, penicillins, diuretics, opioids - food and food additives: nuts, fish, shellfish, eggs, chocolate, strawberries, tomatoes, cheese, etc - chemical/contact: latex, ammonium, persulfate, perfumes, plants, cosmetics, textiles - other misc: parasites, arthropod bites, malignancy, hormones, autoimmune
56
URTICARIA Diagnosis
- detailed H&P - 5 Is: infections, ingestants, inhalants, injectants, internal disease - contact/chemical - allergen testing - stool cultures/sinus xray - autoimmune/CT work up - malignancy work up - thyroid disease
57
URTICARIA Differential dx
- acute: drug eruption, viral exanthem, insect bites, angioedema, urticaria vasculitis, pityriasis rosea - chronic: erythema multiforme, bullous pemphigoid, Lyme disease, urticarial vasculitis
58
URTICARIA Treatment
- refer to derm if recurrent or chronic - treat underlying condition - antihistamines preferred initial Tx: 1st generation (sedate) = hydroxyzine and diphenhydramine (benadryl); 2nd generation (low sedating) = fexofenadine (allegra), certrizine (zyrtec), loratadine (claritin) - topicals: tepid or oatmeal bath - for difficult cases: H2 receptor antagonists, corticosteroids, tricyclic H1 and H2
59
ANGIOEDEMA Etiology
- abrupt and evanescent swelling of the skin, mucous membranes, resp/GI tracts - deeper rxn: more diffuse swelling than hives; deeper form of urticaria that involves deep dermis and subQ tissue - caused by increased vascular permeability
60
ANGIOEDEMA Predisposing conditions
- sex: F >M | - may be with or w/o family history, urticaria, systemic symptoms
61
ANGIOEDEMA Clinical appearance
- subQ tissue: face including lips, hands, arms, legs, genitals - GI organs: stomach, intestines, bladder; nausea, vomiting, diarrhea - upper airway: dyspnea and dysphagia - non-pitting swelling - may have pain or burning - pruritus typically absent - marked periorbital/perioral swelling
62
ANGIOEDEMA Diagnosis
- detailed H&P - possible biopsy - immunologic studies deferred to allergy or derm - some recommend CBC/diff, basic metabolic panel, thyroid
63
ANGIOEDEMA Differential dx
- anaphylaxis - urticaria - cellulitis - erysipelas - contact dermatitis
64
ANGIOEDEMA Treatment
- acute severe attacks: epinephrine and antihistamines - refer to derm/allergist - ID bracelets w/ Dx - Epi Pen - hereditary angioedema: replacement with C1 inhibitor concentrate; fresh frozen plasma - intense support may be necessary depending on Sxs
65
ERYTHEMA MULTIFORME
- common, acute, might be recurrent, inflammatory, hypersensitivity disease - EM minor: localized skin eruption with no mucosal involvement - EM major: more severe mucosal and skin (eg SJS or TEN - potentially life threatening disorders, derm emergencies)
66
ERYTHEMA MULTIFORME Predisposing conditions
- M>F slightly | - 20-40 y.o; 20% in adolescents
67
ERYTHEMA MULTIFORME Causes
- most common is herpes simplex virus, Mycoplasma pneumoniae, acute URI - medications - other infection (bacterial/viral/fungal) - contact allergens - flavoring, preservative, food - immunologic disorders; connective tissue diseases - mechanical (tattoos)
68
ERYTHEMA MULTIFORME Clinical features
- prodrome: malaise, fever, itching, burning, couch - numerous lesions: target lesions, erythematous macules and papules, urticarial-like, vesicles, bullae - primary lesion: small dull red macule with central papule/vesicle that may flatten and clear - symmetrical on palms, soles, extensor surfaces of forearms/legs - with or w/o burning, Koebner phenomenon - mucosal lesions - heal w/o scarring
69
ERYTHEMA MULTIFORME Diagnosis
- detailed H&P - biopsy - helpful if dx uncertain - HSV PCR if lesions suggestive - more systemic work-up in severe cases
70
ERYTHEMA MULTIFORME Differential Dx
- urticaria - Stevens Johnson syndrome - toxic epidermal necrolysis - drug eruption - bullous pemphigoid
71
ERYTHEMA MULTIFORME Treatment
- most mild cases don't require Tx - antiviral therapy - antihistamines for pruritus - systemic steroids for widespread disease - soothing mouthwashes - symptomatic for wounds - topical antibiotics - supportive care: IV fluids w/ electrolytes if severe - refer to derm
72
ERYTHEMA NODOSUM
- hypersensitivity reaction to various triggers - inflammatory reaction in the panniculus - self limiting - 55% cases are idiopathic
73
ERYTHEMA NODOSUM Predisposing conditions
- age 18-34 years - 5F:M in adults; kids affected equally - bacterial: strep infections, TV, yersinia, salmonella, shigella - fungal: coccidiomyosis - viruses: hep B, HSV, Epstein Barr - parasitic: giardiasis, ascariasis - drugs: sulfonamids, oral contraceptives, penicillin - inflammatory conditions - malignancy: lymphoma, leukemia, renal cell carcinoma - pregnancy
74
ERYTHEMA NODOSUM Clinical features
- lesions start as poorly defined, red, firm, tender subQ nodules, 2-6cm that fade over 1-3 weeks, do not scar - extensor surfaces, bilateral but not symmetric, most common on pretibial surfaces - new lesions appear for 3-6 weeks - ankle edema and leg pain are common - may have prodrome of flu-like Sxs, fever, myalgias a few weeks before or with onset of lesions - arthralgia > 50%
75
ERYTHEMA NODOSUM Diagnosis
- detailed H&P - biopsy if atypical and include fat - throat culture/rapid strep - complete CBC - CXR - PPD - ESR - stool culture with GI sxs
76
ERYTHEMA NODOSUM Differential Dx
- erysipelas - cellulitis/thrombophlebitis - acute urticaria - physical abuse - Henoch Schonlein purpura
77
ERYTHEMA NODOSUM Treatment
- treat underlying condition and stop offending medication - NSAIDs - rest - cool wet compresses - potassium iodide or corticosteroids (only if severe or recurrent)