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Elizabeth (Lisa) Swanson, MD
Advanced Dermatology
 Can be deep (look bluish) or superficial (look red) or a
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combination
Typically not present at birth or can be a slightly pink
area
Grow until the age of 8-12 mos and then involute
slowly by 10% per year (all of them are gone by age 10)
More common in girls, more common in premies,
more common in mult gestation births
In most cases, they are a benign nuisance but they can
cause some big problems
 Hemangiomas on the lip,
eyelid and nose are very
important to think of
separately both for
functional and cosmetic
reasons
 If the hemangioma
crosses the vermilion
border of the lip,
damages the cartilage of
the nose, or occludes an
eye, the consequences
can be disastrous
 Large hemangiomas and
ones in certain locations
(perineum, midline) are
prone to ulceration
 Ulceration is incredibly
painful for the baby and
leads to permanent
scarring
 Hemangiomas in the
“beard” distribution
can have subcutaneous
involvement in the
larynx and can
threaten the airway
 Pelvic and lumbosacral
hemangiomas can be a
sign of a tethered cord or
other neurologic
abnormality
 Always get an MRI (or
ultrasound if child is less
than 3 mos old)
 Propranolol 2 mg/kg/day divided TID with food
 Side effects include hypoglycemia, decreased HR and BP,
inc wheezing with resp infections
 Prednisolone 2 mg/kg/day given in the AM
 Vincristine is largely outdated
 Vascular laser- can be used for ulceration, for residual
telangiectasia
 Surgery can have its place
 Topical beta blockers- Timolol, Propranolol
 Must evaluate for PHACES
 Post fossa abnorms
 Hemangioma
 Arterial anomalies (mainly
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head and neck)
Cardiac anomalies and
coarc of the aorta
Eye abnormalities
Sternal clefting
Do an MRI/MRA of the
head and neck and an
ECHO in these babies
 Rapidly Involuting
Congen Hemangiomas
and Noninvoluting
Congen Hemangiomas
are present at birth and
typically can be big
 RICHes go away quickly
 NICHes never go away
and many opt for
surgical removal
 Flat pink-purple patches
that do not blanch
 Present at birth
 If on the upper eyelid or
near the eye, baby should
see ophthalmology to
eval for glaucoma
 Can be treated with
pulsed dye laser (starting
at 6 mos old, every 6-8
wks)
 Babies with extensive PWS,
esp in V1 and V2
distribution, should be eval
for Sturge Weber
 Sturge Weber is triad of
PWS, glaucoma, seizures
 Basically ophthalmology
appt is all they need
 MRI scanning is
controversial, most wait to
see if they are going to have
seizures
 Present at birth as an
orange-tan hairless
patch
 At puberty it can
become bigger and
more lumpy
 Has a risk of benign
and malignant
neoplasms (BCC)
within it
 Can choose excision or
yearly visits to derm
 Present at birth, usually as shallow ulceration and then
the ulceration heals as a scar
 Consider ultrasound if lesion is large, if there are
multiple, and if there is the “hair collar sign”
 Usually people have them cut out because of the
hairlessness
 Small congenital nevi
have <1% chance of
developing into
malignancy
 Patients have option of
excision vs yrly visits to
derm
 Questionable role of
laser
 These patients belong in
a pediatric derm’s office
 6% risk of melanomatends to be in nevus
overlying spine and
tends to occur in 1st year
of life
 Definite risk of
neurocutaneous
melanosis and most
would obtain MRI
 Autoimmune attack of hair follicles
 Produces circular nonscarring patches of alopecia
 Can affect scalp, eyebrows, eyelashes, body hair
 Three possible courses of disease
 One time event with complete recovery
 Complete recovery with each episode but recurrences
every few years
 Progression of disease to alopecia totalis or universalis
(rare)
 Family/personal history of alopecia areata
 History of eczema
 Pattern of alopecia (ophiasis has bad prognosis)
 Speed of alopecia (the quicker it happens, the worse it
is)
 Minimal association with thyroid disease, diabetes…if
child is otherwise healthy, no need to check
 Squaric acid contact therapy
 DPCP contact therapy
 Light therapy
 Anthralin
 Intralesional steroids
 Pulse steroids
 Sulfasalazine?
 Clobetasol solution and Rogaine?
 Intentional/unconscious
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hair pulling
Islands of sparing
Hair of different lengths
Usually 7-13 yr olds
Typically high achievers
Can do shave test to
differentiate from
alopecia areata
 Red and crusty areas on scalp, usually with associated hair
loss unless you see it early on
 Do fungal culture to diagnose
 Tell pt and family members to use Nizoral shampoo to help
prevent spread from spores (not a treatment, just to
prevent spread to other family members)
 MUST treat with oral antifungals
 Griseofulvin 20-25 mg/kg/day divided BID for 6 weeks
 Lamisil 125-250 mg daily for 3 weeks (bad for microsporum)
 Itraconazole 100-200 mg daily for 3 weeks
 Griseo and Itra come in a syrup
 Annular, erythematous, scaly lesion with raised red
edge is the hallmark
 Kids get it from other kids or animals
 Very common in wrestlers, gymnasts
 To diagnose: KOH or fungal culture
 Topical antifungal- ketoconazole, spectazole, terbinafine
BID. AAA and one inch around it. Once it resolves, cont
treating for 1-2 weeks to ensure eradication
 Oral antifungal
 Must be used if steroids have been used previously or if there is
evidence of a fungal folliculitis
 Griseofulvin 10-20 mg/kg divided BID for 3 weeks
 Terbinafine 125-250 mg daily for 1-2 weeks- doesn’t work great for
microsporum species (if family dog is suspected, do not use)
 Itraconazole 100-200 mg daily for 1-2 weeks
 More common in kids than adults
 Typically triggered by a strep infection
 Ask about family history
 Patients usually continue to have lifelong problems
with psoriasis
 Topical medicines
 Clobetasol ointment
 Dovonex ointment
 Tazarotene
 Protopic
 Scalp solutions- Clobetasol, DermaSmoothe- always
recommend a salacylic acid containing shampoo
(Neutrogena T Sal, Baker’s P and S)
 Light therapy
 Systemic options- Methotrexate, Enbrel
 Triggered by a virus
 Lasts up to 8-10 weeks
 In african americans, it looks more papular…can be
tricky to identify
 Can treat with Erythromycin- varying reports of
efficacy
 Topical steroids will help if it’s itchy but won’t help
clear up the rash
 Very common, tends to run in families, can coexist
with asthma/allergies
 Typical distributions based on the age of the child
 Very itchy (“the itch that rashes”)
 Very important to treat- can lead to weight loss, failure
to thrive, sleep disturbances (for the whole family)
 Topical steroids are mainstay- use OINTMENTS so they
don’t sting
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Hydrocortisone 2.5%
Triamcinolone 0.1%
Fluocinonide 0.05%
Clobetasol 0.05%
Topical steroid burst
Wet dressings
 Protopic/Elidel are very useful
 Always emphasize the importance of sensitive skin care
(ALL detergent, no fabric soft and dryer sheets, Dove or
cetaphil soap) and moisturization (Vaseline or Vanicream)
 Occasionally light treatment
 Occasionally systemic meds- Methotrexate, Imuran,
Cellcept
 2 out of 3 kids grow out of it (somewhat) by age 5
 Pretty common
 Think of it when eczema
just not getting better
 Treat with oral
antibiotics
 I tend to get culture
 If recurrently
problematic, can
recommend bleach baths
2-3 times weekly (1/2 cup
bleach to one full tub
water)
 Teeny blisters, often on palm or lateral sides of the
fingers
 Pts sometimes have hyperhidrosis too
 Treat with topical steroids +/- drysol antiperspirant
 Coin shaped
 Can look like tinea
 Typically requires high
potency steroidsFluocinonide or even
Clobetasol
 Typically kids age 1-5
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yrs old
Classically on the
ball of the foot, big
toe and pinky toe
Not eczema and not
a fungus
Improves with time
No real treatment
 Associated with sensitive skin and eczema
 More noticeable in the summer because of tanning
 Goes away on its own
 Can try Hydrocortisone 2.5% oint BID or Protopic BID
if patient really wants treatment
 Differential diagnosis:
 Vitiligo- PA is HYPOpigmented, vitiligo is Depigmented
 Tinea Versicolor- affects the face in kids (unlike in
adults). Typically has areas of hypo and hyper
pigmentation, tends to have a pink tone with scale, but
can be difficult to tell
 Autoimmune destruction of pigment producing cells-
produces DEpigmented patches
 Can be widespread or segmental
 Treatment is difficult, but options include:
 Clobetasol once daily
 Protopic twice daily
 Light therapy
 Excimer laser treatments
 Typically on trunk of teens and young adults, but
frequently on the face of kids
 KOH can show spaghetti and meatballs appearance to
prove it
 Treatment options
 Selsun Blue shamp00- leave on 10 minutes in shower
 Ketoconazole 2% cream BID
 Ketoconazole 400 mg once (then work out) and repeat
in one week
 Itraconazole 400 mg once
 Fluconazole 400 mg once
 Recurrences are common and it takes awhile for pigment
to return to normal
 The target consists of 3 concentric areas of
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discoloration- the outer red wheal, an area of
blanching, and a central red-purpuric macule
Almost always the result of a virus (rarely a medicine)either a viral illness or HSV
Self limited, but can be uncomfortable esp because of
the oral lesions
I typically prescribe Prednisone 1-1.5 mg/kg/day for 7
days
If triggered by HSV, can be recurrent- can be a reason
for suppressive therapy
 Due to meds- Bactrim, antiseizure meds, PCN
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antibiotics
Evolves rapidly
Eyes and mouth tend to start having problems first
Skin lesions usually not targetoid. Tend to be vague
erythematous macules and patch at first. Then
widespread blisters develop
Can lead to permanent scarring in eyes, mouth,
esophagus, GU system, skin
Pts need early hospitalization with IVIG or prednisone
 Potentially very serious…any baby with clustered
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blisters on a red base should be hospitalized and
started on IV acyclovir
First 4 weeks of life, usually in 1st week
Fetal scalp monitoring is a risk factor
Can cause hepatitis, pneumonitis, meningitis
Differential would include bullous impetigo, possibly
candida, but HSV is most serious and should be
treated while cultures are cooking
 Presents with red, slightly erosive and crusty rash
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around mouth and in folds (axilla, groin)
Due to a staph (or strep) infection elsewhere- typically
oropharyngeal
Rash occurs due to a toxin released by the bacteria
Patients have a fever, seem sick and have remarkably
sensitive skin (almost like they are sunburn…it really
hurts if you just touch them)
Treat for staph and strep and use vaseline on the skin
Only other thing that looks like this is Zinc deficiency
 Cause is unknown
 Classically around mouth, around eyes, in crease of nasal
ala
 Consists of small pink papules, pustules, and oftentimes
some pink and scaly (dermatitis-like) areas
 Frequently mistreated with topical steroids and topical
steroids make it worse
 Treatment
 Elidel 1% cream BID in kids
 Metrogel 1% gel daily in adults
 Oral antibiotics- Minocycline, doxycycline if greater than 9
yrs old; azithromycin or amoxicillin if less than 9 yrs old
 Recurrences are common
 Interstitial infiltrate of lymphs in the dermis create an
annular lesion with a raised, red border without scale
 Typically occurs on dorsal hands, dorsal feet, ankles
 Subcutaneous GA is most common in kids and
presents as painless subcutaneous nodules typically on
the scalp and lower extremities
 Tends to resolve eventually on its own. High potency
steroids, IL steroids, or light therapy can be used.
 Frustrating for patients and doctors
 Treatment options are many (because no one
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treatment is fantastic)
Liquid nitrogen- hurts
Cantharadin PS- doesn’t hurt, from a blister beetle
Soak, Scrape and Tape with 17% Sal Acid and duct tape
Squaric Acid contact therapy
Candida ag injections
Bleomycin
Cimetidine (in combo with other txs)
Surgery?
Aldara?
 Usually m0re frustrating than common warts
 Especially common in teenage girls that use tanning
beds, often on the legs (shaving is a factor)
 Treatment options
 Liquid nitrogen
 Cantharadin PS
 Aldara
 Veregen
 Retin A
 Little balls of capillaries, typically thought to occur as
result of trauma
 Best treatment is shave removal with cautery of the
base
 Small lesions can be treated with Aldara MWF at
bedtime with relatively good results
 I favor removing them with path eval because spitz
nevi and even melanoma are in the differential
diagnosis
 Dome shaped pink
papule
 Technically benign but
their histology and
behavior is a bit
controversial
 Used to be called
“juvenile melanoma”
 Treatment is
controversial
 Classically pink-yellow
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papule
Goes away- typically
by age 5
If excised, it frequently
recurs
If just one, no real
associations
If several, pt should
have eye exam
Questionable link with
neurofibromatosis
 Very common on the
face of children
 Most go away
eventually
 Can be treated with
vascular laser
 Firm white-blue
subcutaneous nodule or
plaque
 Benign cystic lesion that
calcifies
 ½-2/3 go away
 Only treatment is
surgical excision
 Look like café au lait
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macules but tend to be
slightly raised and
slightly more pink
Positive darier’s sign
Completely benign and
will go away
Internet can scare
parents
Avoid mast cell
degranulators
 Autoimmune destruction
of a mole producing a
depigmented halo
 Normal in kids,
abnormal in adults
 Associated with vitiligo