Miscellaneous Disorders - Exam 2 Flashcards

1
Q

______ are localized asymptomatic skin disorder manifesting with hyperpigmented, velvety plaques typically located in flexural and intertriginous regions. What are they commonly seen with? What race?

A

Acanthosis Nigricans

common seen with skin tags

African Americans 25x more likely than whites

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2
Q

What is the likely etiology of acanthosis nigricans?

A

Stimulation of insulin-like growth factor receptors and tyrosine kinase receptors on keratinocytes and fibroblasts

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3
Q

What are the 8 types of acanthosis nigricans?

A

obesity
malignancy
drug induced
syndromic
acral
unilateral
benign
or
mixed

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4
Q

What dz are closely related to AN?

A

diabetes
insulin resistance
high body mass index (BMI)
metabolic syndrome
polycystic ovarian syndrome (PCOS)

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5
Q

If AN is related to malignancy like going to be ______

A

gastric carcinoma

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6
Q

What drug is closely related to AN?

A

Niacin MC

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7
Q

What are the 2 causes of syndromic AN?

A

A = Hyperandrogenism, insulin resistant, acanthosis, acromegaly

B = Autoimmune and Diabetes

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8
Q

Where are acral AN commonly found?

A

Elbows, knees and knuckles

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9
Q

What are unilateral AN related to?

A

Nevoid (Epidermal Nevus)

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10
Q

What is benign AN related to? What is mixed AN?

A

Rare autosomal dominant type

mixed: any 2 or more of the AN types

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11
Q

Where is AN typically seen?

A

It is typically seen in the neck folds (“dirty neck” appearance) and axillae

The inguinal and inframammary folds, antecubital and popliteal fossae, and elbows and periumbilical region may also be involved

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12
Q

Where are rare sites of involvement for AN? If you see a rarely form of AN, what should you think?

A

Rarer sites of involvement include velvety plaques on the knuckles, palms (“tripe palms”), soles, eyelids, periorally, near mucosal surfaces, or generalized

These rarer forms of AN are more closely related to malignancy

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13
Q

What will AN look like on the oral mucosa/lips?

A

have thickening and papillation and usually lack hyperpigmentation

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14
Q

How do you dx AN? What tests could you order?

A

clinical dx

AIC or fasting plasma testosterone/dehydroepiandrosterone sulfate

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15
Q

What is the tx for AN? What topical treatments are helpful?

A

tx the underlying cause

usually insulin insensitivity

topical: topical retinoids and/or vitamin D analogs may help improve appearance of lesion

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16
Q

In a pressure injury, where does the breakdown of skin occur? What is the pathophys?

A

Breakdown of the skin and underlying tissue resulting from unrelieved soft tissue pressure between bony prominence and external surface

non-relieving pressure/shearing forces results in diminished blood supply leading to cell death

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17
Q

What are the risk factors for a pressure injury? Which one is MC?

A

impaired mobility (MC)
contractures/spasticity
impaired sensation
aging skin
incontinence/fistula (skin maceration)
malnutrition
hypoproteinemia
anemia

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18
Q

What are the common locations for a pressure injury? Who is the MC pt?

A

sacrum/hip (70%)- MC

LE: malleolar, heel, patellar, pretibial

MC in acute hospitalized patients: think ortho and ICU pts

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19
Q

Pressure injuries place patients with same risk factors at _____ greater risk of death

A

4.5 times

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20
Q

In a pressure injury, where is the wound wider?

A

wider at the base and the inspection can be deceiving to the untrained eye

may require pain medication administration for adequate exam

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21
Q

When is NPUAP staging used in pressure injuries? Does it change as it heals?

A

used for initial evaluation and diagnosis and for description and documentation purposes only. NOT used in the evaluation of wound progression

stage is NOT changed upon healing (aka reverse staging)

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22
Q

**Draw the different staging pressur ulcers chart

A
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23
Q

_______ intact skin and non-blanchable hyperemia. What stage? What does a blanchable lesion mean?

A

stage 1 pressure injury

blanchable erythema, skin firmness, change in sensation or temp may precede stage I injury

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24
Q

What stage?

A

stage 1 pressure injury

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25
Q

intact blister or loss of epidermis with exposed dermis and subq tissue is NOT visible. wound bed is viable, pink/red, moist and NO granulation or eschar tissue. What stage?

A

stage II

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26
Q
A

stage II pressure injury

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27
Q
A

stage II pressure injury

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28
Q

full thickness skin loss, exposed subcutaneous tissue/adipose
no fascia, muscle, tendon, ligament, cartilage or bone visible, may have scar tissue, may have eschar, may slough and have epibole

What stage?
What is an epibole?

A

stage III pressure injury

epibole- rolled wound edge

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29
Q
A

stage III pressure injury

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30
Q
A

stage III pressure injury

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31
Q
A

stage III pressure injury

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32
Q

full-thickness skin/tissue loss
exposed fascia, muscle, tendon, ligament, cartilage and/or bone
eschar tissue
epibole
undermining/tunneling may be present

What stage?

A

stage IV pressure ulcer

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33
Q
A

stage IV pressure ulcer

34
Q

full thickness skin and tissue loss obscured by slough or eschar
removal of obscuring tissue will reveal

What stage?
What should you NOT do?

A

unstageable

usually stage III or IV if obscuring tissue was removed

Do NOT remove a stable eschar for staging purposes

35
Q

generally intact skin
deep red, maroon, or purple discoloration
blood filled blister
unable to visualize

What stage?

A

Suspected deep tissue injury

necrotic/granulation tissue, subcutaneous tissue or deeper structures

36
Q
A

Unstageable pressure injury

37
Q
A

suspected deep tissue injury

38
Q
A

suspected deep tissue injury

39
Q

What labs should you order in a pressure injury?

A

ESR, WBC

wound culture via punch bx

bone bx if concerned for osteomyelitis

40
Q

What is the broad tx of a pressure injury?

A

reduce/eliminate underlying risk factors

redistribute pressure: reposition every 2 hrs or sooner and bed elevation to < 30 degrees, minimize friction/shear forces with proper transferring and turning techniques

remobilization

Clean skin with mild cleansing agents and keep dry

control pain

abx if indicated

41
Q

What is the tx for stage I pressure injury? stage II? stage III/IV?

A

Stage I: cover with transparent film for protection

Stage II: transparent or hydrocolloid dressing

Stage III/IV: debridement

42
Q

**What is the CI for hydrocolloid dressing?

A

CI in active infection

43
Q

What are the 4 things you need to monitor for in pressure injury healing?

A

size in cm

exudate amount

tissue type (sloughing, eschar)

Score (0-17) will decrease with healing

44
Q

How long does it usually take for a stage I or II pressure injury to heal? stage III or IV? What is the MC complication?

A

Stage I & II heal in 1-2 wks

Stage III & IV health in 6->12 wks

MC complication: infection

45
Q

What is Hidradenitis suppurativa? What areas are common?

A

Chronic suppurative disease of the apocrine gland bearing skin areas

axillae, inguinocrural and anogenital regions; scalp(rarely)

46
Q

What is the MC pt with HS? What are the risk factors? **What are the 2 RF specifically mentioned in class?

A

Females> Males
Onset: beginning at puberty

occlusive dress, trauma, obesity, smoking, host defence defects, hormones, genetics

**obesity and smoking

47
Q

What is the pathophys behind HS?

A
  1. perifollicular inflammation
  2. hyperkeratinization of follicular epithelium with occlusion and dilation of the follicle
  3. follicular rupture and release of intrafollicular debris into the dermis with increased inflammation
  4. formation of tunnels filled with debris and/or fluid that connect to the surface of the skin and to the base of other ruptured follicle
48
Q

Open comedones are characteristic
Nodules with sinus tracts (inflamed or noninflamed)
Abscesses
Scarring
Sinus tracts lead to dermal contractures and ropelike elevation of the skin

What am I?
What is usually in the hx?

A

Hidradenitis suppurativa (HS)

History of recurrent painful suppurative lesions which heal leaving scars

49
Q

What are 3 complications of HS?

A

Secondary infection

Fistulas to urethra, bladder, and/or rectum

Chronic inflammatory reactions

50
Q

What are the tx options for HS?

A

Intralesional glucocorticoids

Oral antibiotics

Isotretinoin

Biologics

Surgery

51
Q

What is the immediate tx of acute HS lesions?

A

Intralesional steroid followed by I&D abscesses

oral abx: B-lactamase PCN, Cephalosporins, Augmentin, Clindamycin

oral steroids to decrease pain/inflammation

52
Q

What is the tx for recurrent HS lesions?

A

abx PLUS retinoids (clinda PLUS isotretinoin)

biologics: adalimumab (Humira) or infliximab (Remicade)

53
Q

What is the tx for chronic recurrent HS lesions?

A

Surgical Treatment: small excision of chronic recurrent nodules or sinus tracts

complete excision of lesions with wide margins

address psychosocial complications

54
Q

What are the lifestyle modifications to education your pt with HS?

55
Q

______ is the abnormal response to light, usually sunlight, occurring in minutes, hours, or days of exposure and lasting weeks, months and even longer. What are the 3 types?

A

photosensitivity

sunburn
rash
urticarial

56
Q

______ Chronic repeated sun exposures over time result in polymorphic skin changes that have been termed dermatoheliosis or photoaging

A

chronic photosensitivity

57
Q

A _____ type response with skin changes simulating a normal sunburn such as in phototoxic reactions to drugs or phytophotodermatitis

A ____ response with macules, papules, or plaques, similar to eczematous dermatitis

_____ responses are typical for solar _____

A

sunburn

rash

Urticarial, urticaria

3 different types of photosensitivity

58
Q

______ A phototoxic reaction that presents as an acute, delayed, and transient inflammatory response of normal skin after exposure to UVR from sunlight or artificial sources

A

acute sunburn

59
Q

Pruritus, pain and tenderness
may develop headache, malaise even after short exposure

What am I?
What is a severe presenation?

A

acute sunburn

If severe sunburn, patient can present “toxic” with flu like illness
Fever, chills, fatigue, weakness, tachycardia

60
Q

When does an acute sunburn s/s typically present? Describe it in words

A

Develops after 6 hours and peaks after 24 hours

Confluent bright red erythema confined to sun-exposed areas and sharply marginated at the border between exposed and covered skin. May have vesicles and bullae. As edema and erythema fade, vehicles and blisters dry to crusts, which then shed

61
Q

What is the tx for an acute sunburn?

A

Cool, wet dressings and topical glucocorticoids
Aloe Vera
NSAIDs

62
Q

What is the tx for a severe acute sunburn?

A

Bedrest and oral fluids

“Toxic” patients may require hospitalization for IV fluid replacement

63
Q

What are the 3 prevention strategies for an acute sunburn?

A

SPT I/II should avoid sun exposure between 10AM and 2PM

Adequate sunscreen use and proper reapplication

Clothing - UV-screening cloth garment

64
Q

_____ is an adverse reaction of the skin that results from an interaction between UVR with a chemical or drug. What are the 2 types?

A

Photosensitivity: Drug/Chemical Induced

Phototoxic reactions

Photoallergic reactions

65
Q

_____ a photochemical reactions that presents like an irritant contact dermatitis or sunburn. What is the associated timing? What is the pathophys?

A

phototoxic reactions

subtype of Photosensitivity: Drug/Chemical Induced

minutes to hours onset of eruption after exposure

direct tissue injury

66
Q

__________ is formed that initiates an immunologic response, manifests in skin as a type IV immunologic reaction and presents like an allergic eczematous contact dermatitis. What is the associated timing? What is the pathophys?

A

Photoallergic reactions

subtype of Photosensitivity: Drug/Chemical Induced

24-48 hours onset of eruption after exposure

Type IV delayed hypersensitivity response

67
Q

What is the tx for an phototoxic reaction?

A

remove offending agent and tx conservatively

think sunburn

68
Q

What is the tx for an photoallergic reaction?

A

remove offending agent

antihistamines

steroids

treat like contact derm

69
Q

_____ is also called dry skin or asteatosis, refers to a condition of rough, dry skin texture with fine scale and occasionally fine fissuring. What will the pt complain of?

A

xerosis

Often pruritic

70
Q

What is the pathogenesis of xerosis?

A

Pathogenesis involves a decrease in the amount of lipids in the stratum corneum and a deficiency in the water-binding capacity of this layer

71
Q

The incidence of xerosis increases with _____. nearly all individuals over the _____ have some degree of xerosis

A

age

age of 60

72
Q

In more advanced xerosis, the _____ may begin to exhibit a _____ pattern of superficial cracks and fissures with erythema

A

stratum corneum

polygonal

73
Q

Where are the MC locations of xerosis?

A

lower extremities, trunk, and dorsal hands, usually sparing the head, neck, palms, and soles

74
Q

What questions/pt educations points are important in xerosis?

A

Inquire about bathing habits (frequency, type of soap used, water temperature)

Hot water, frequent or prolonged bathing, and the use of soaps worsen xerosis

Take a complete medication history

encourage bathing in luke-warm bathing and to apply moisturizers within 60 seconds of getting out of the shower

too frequent bathing can also exacerbate factors

humidifiers

mild soap substitutes, nothing with fragrance

75
Q

How do you dx xerosis?

A

clinical dx

76
Q

What am I? How is it inherited? What is it?

A

ichthyosis

autosomal dominantly inherited condition of abnormal cornification leading to scaling and desquamation and presents as fine, fish-skin-like scale.

77
Q

When is Ichthyosis more commonly seen? What age range does it usually begin?

A

It is more prominent in winter and in climates with low relative humidity

The condition usually begins in childhood between 3 and 12 months of age and follows a favorable course in which the scaling alleviates in intensity by adulthood.

78
Q

What are the tx options for Ichthyosis? Where is it most prominent? You should look for _______ and _____

A

Hydration, lubrication, and keratolysis are the mainstays of therapy

The condition is usually most apparent on the extensor extremities.

Look for accentuated palmar creases and scaly palms.

79
Q

How do you dx Ichthyosis? What does acquired ichthyosis make you think?

A

clinical dx but can skin bx

Cases of acquired ichthyosis warrant a search for an underlying systemic disease or malignancy

80
Q

What is the tx for Ichthyosis?

A

Emollients are the mainstay of therapy. Creams applied after bathing help the epidermis retain water

non-drying soaps and cleansers

soaking with mechanically exfoliating

humidifiers

may use keratolytic agent containing an alpha hydroxy acid, salicylic acid, or urea can be used but only if localized areas, topical retinoids, topical vit D, mid-potency steroid cream