CH 22 Derm in Infant Flashcards

1
Q

hemangioma patho

A

-BENIGN tumor of endothelium
-local proliferative process that affects endothelial cells
-perhaps genetic mutation of epithelial regulation

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2
Q

hemangioma presentation

A

NOT present at birth
grew rapidly from first days of life to 6 months
-slow proliferation for 6-12 months then involution/shrinks phase from 12 months to 3-6 years
-light port wine stain (1/3 have it)

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3
Q

hemangioma management

A

-depends on location, risk of complication, scarring, ulceration
-can slow growth with: oral propranolol, systemic corticosteroids
-vinscristine, interferon alpha injection into lesion
-uncommon: injected steroids, laser therapy
-watchful waiting

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4
Q

when would you do watchful waiting for hemangioma?

A

-for active nonintervention for superficial lesions in low function areas (thigh, upper arm)
-will involute slowly through early childhood

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5
Q

port wine lesion patho

A

disorder of dermal capillaries and post capillary venules
- can be a/s with other congenital or genetic syndromes (Sturge-Weber (if on face) or AV malformation syndrome)

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6
Q

port wine lesion presentation

A

ALWAYS present at birth
-blanchable (vascular) from red to dark pink, grows proportionally with child
-will darken and become more nodular as child grows and not regress
-lesions on face follow trigeminal nerve branches

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7
Q

port wine lesion considerations

A

genetic and congenital syndrome when lesions are present, esp if face and eyelid involved

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8
Q

port wine lesion management

A

Referrals:
-Derm for pulse dye laser therapy (lightens but doesn’t remove)
-ophthalmology if eyelids involved (glaucoma risk)
-neuro (on face = seizures)

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9
Q

mongolian spot patho

A

diffuse melanocytes within dermis
- interrupted movement of melanocytes during
fetal development from neural crest to epidermis

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10
Q

mongolian spot presentation

A

-blue-black-gray macular lesions (lower back, butt mostly)
-single or multiple lesions
NONtender (not bruises), no malignancy potential
-Asian, natives, Africans (rare in europeans)

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11
Q

mongolian spot management

A

no treatment! lighten over time and often disappear during childhood

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12
Q

milia patho

A

retention of keratin and sebaceous material in pilosebaceous glands

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13
Q

milia presentation

A

raised white bumps mainly on nose and cheeks

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14
Q

milia management

A

no treatment! resolves spontaneously 1-2 months
-reassurance to parents
-don’t pick or remove it = scar

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15
Q

erythema toxicum neonatorum (ETN) path

A

unknown
-thought to be immaturity of pilosebaceous glands (hair follicles)

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16
Q

erythema toxicum neonatorum presentation

A

-occasionally at birth, usu appears w/in first 2 days and resolves by day 5-7
-“flea bitten” appearance
-erythematous papules that progress to pustular lesions

17
Q

erythema toxicum neonatorum management

A

observation, no treatment indicated
-resolves sponatenously
-reassurance!
30-70% full term infants will experience these lesions

18
Q

atopic dermatits (eczema) patho

A

-impaired epidermal layer, with impaired barrier = irritants get into dermis
-decreased water content due to poor barrier
-itch-scratch cycle worsens condition
-genetic component

19
Q

atopic dermatitis presentation

A

-itchy, xerosis, red, crusty, extensor surface, face, neck, scalp
-child (2-12 years): lichenification of flexure surfaces (places the BEND: popliteal space, antecubital fossa)
-adult (>12 years): similar^, hand/feet

20
Q

atopic dermatitis management

A

3 prongs:
1. eliminate triggers
2. hydrate (use thick creams or ointments daily, no lotion bc it dehydrates when it evaporates)
-minimal soap use! bathe only 2-3x/week
-best hydration cream: Crisco cooking fat
3. control itch (sedating antihistamines qhs, topical cortiocs for flares)

21
Q

acne neonatorum patho

A

-from stimulation of sebaceous glands by maternal or infant androgens (acne is testosterone driven)

22
Q

acne neonatorum presentation

A

-face, forehead, nose, cheeks
-starts first months of life, lasting 1-2 months (longer than ETN) til ~4 months w/o scarring

23
Q

acne neonatorum management

A

-self-resolving
-don’t pick or squeeze lesions
-benzoyl peroxide 2.5% if extensive & few months
-affects 20% infants

24
Q

seborrheic dermatitis aka Cradle Cap patho

A

-usu in areas of dense sebaceous gland (scalp, face, groin, underwarms)
-overstimulation of sebum production
-possibly lipid dependent yeast

25
seborrheic dermatitis infant - cradle cap presentation
-erythematous plaques -greasy with yellow scales -seen in infants and throughout life
26
seborrheic dermatitis infant - cradle cap management
-infant scalp treatment = apply emollient (petrolatum, vegetable, mineral oil) overnight, then remove plaque with soft brush -for other parts of body = ketoconazole 2% cream QD x 1 week or low dose hydrocortisone 1% QD x 1 week
27
keratosis pilaris patho
genetic disorder of hyperkeratinization of hair follicles of the skin
28
keratosis pilaris presentation
-rough skin texture (chicken skin) - usu asymptomatic except of occasional pruritus - poor cosmetic appearance - upper arm most common
29
keratosis pilaris management
-no cure or universal effective treatment available -regular skin are regimen with lotions and creams can lead to improvement -prevent excessive skin dryness with mild soapless cleansers and lubrication w/ moist lotions -lactic acid lotions, alpha hydroxy acid lotion, urea cream, salicylic acid, topic steroid creams, and/or retinoid acid products (Differin)
30
keratosis pilaris more common in __ and worse in __ weather.
childhood and adolsecents -worsens with cold, dry winter weather (eczema variant) -improves with age
31
1. Parents of Asian ancestry bring in their healthy 1-week-old daughter born at full term for a well child evaluation. Upon examination, you notice multiple non-tender blue-black flat lesions on the lower back and buttocks. The most likely diagnosis is: A. Port wine lesion. B. Milia. C. Keratosis pilaris. D. Mongolian spot.
D Mongolian spots look like a bruise but it's NON tender! african and asian most common -face and anterior trunk is spared. fades during prescale age uncommon in europeans
32
2. Which of the following is false regarding hemangioma in infants? A. Almost always present at birth B. Systemic corticosteroids can be used to slow growth C. Involves a local proliferative process affecting endothelial cells D. Possibly genetic in origin
A is false. not always present at birth
33
3. All of the following statements regarding keratosis pilaris are accurate except: A. Caused by hyperkeratinization of hair follicles in the skin. B. The condition frequently improves with age. C. Symptoms tend to be worse in hot andhumid environments. D. The condition is genetic in origin.
Eczema varient! so sx's are worse when air is dry and cold / winter time goosebumps rough feeling answer C
34
4. During a well child visit of a 4-weekold girl, the parents express concern about raised white bumps on the infant’s nose and cheeks. The NP recognizes milia and recommends the following approach: A. No specific treatment as this condition will resolve spontaneously. B. Softly scrubbing the area twice daily with a mild moisturizing soap and warm water. C. Daily application of a low-potency corticosteroid cream to the affected area. D. Referral to a pediatric dermatologist.
answer A Milia is common in young babies and will go away on it's own. Discourage any picky = scarring or steroid use.
35
Treatment of atopic dermatitis / eczema present on the cheeks and mouth of an otherwise healthy 4-month-old infant can include all of the following except: A. Moisturizing cream to hydrate the skin. B. Oral antihistamines to reduce itching. C. Topical antimicrobial to prevent infection. D. An appropriate potency topical corticosteroid to control flares.
C don't need antibiotics!!! 1. Hydration 2. LOW potenency for flares for short period of time. 3. Oral antihistamines for itchiness good! ecezma on face is most like in the young child drooling ~ 4 months irritates eczema doesn't matter what part of body, moisturizing is key!