things that make you go hmmmmm…… or it is what it is!
TRANSCRIPT
THIN
GS THAT
MAKE YOU G
O
HMMMMM……
OR
IT IS
WHAT IT
IS!
OBJECTIVES
Identify benign skin lesions with confidence
Identify resources for dermatology education
AND one new thing about management of Hemangiomas
LICHEN STRIATUS
Primary phase
SECONDARY PHASE
Fading and Flattening
-Common 9months to 6 years but can occur earlier or later
-Last 1-3 years
-Relapses of short duration have been noted after complete clearing
NEVUS DEPIGMENTOSIS
Generally present at birth or within several months, sometimes not obvious until sun exposure in fairer skin
Borders can be regular or irregular
Can have whorled appearance
PIGMENTARY MOSACISM /HYPOMELANOSIS OF ITO
Follows blashkos lines
Can be associated with neurologic, skeletal, and/or ocular abnormalities
The hypopigmentation is secondary to hypofunctioning of melanocytes and is thought that mishap ear in embryogenesis is responsible for the mosaicism.
No consistent genetic defect.
Follow up depends on associated abnormalities.
BECKERS
NEVUS
Large, pigmented, hairy nevus
Most commonly noted in adolescence
Benign
Larg
e der
mal
nev
i com
mon
ly s
hould
er b
ut
not e
xclu
sive
ly
MELAN0NYCHIA STRIATALONGITUDINAL MELANONYCHIA
Most commonly seen in individuals with darker skin- especially African-Americans in whom up to 90% may have at least one such streak
The pigmentation extends from the proximal nail fold to the distal margin of the digit
The width may vary from less than 1mm to several mm
But……. (there is always a but)
NAIL MATRIX MELANOMA SHOULD BE CONSIDERED
Worrisome features may include very dark, broad bands AND
Extension of the pigmentation onto the proximal or lateral nail folds (aka Hutchinson’s Sign)
Any patient with this presentation should be referred for nail matrix biopsy which can cause permanent damage to the nail plate
CONFLUENT AND RETICULATED PAPILLOMATOSIS
CRPETIOLOGY: UNKNOWN
Minocin 100mg BID x30 days then qd x 30 days
TERRE FIRMA FORME OR
DUNCANS DIRTY DERMATOSIS
First described by Dr. Duncan in Houston in 1987
At fist glance these patients may appear to have confluent and reticulated papillomatosis (CARP) or acanthosis nigricans
In contrast to derma neglecta soap and water will not wash this off, isopropyl alcohol is necessary
When this condition is suspected, firm, persistent pressure should be applied while rubbing the skin with alcohol.
The cause of terra firma-forme dermatosis is unknown.
PITYRIASIS ALBA (AGAIN)
If you mom think it is fungal…..Do a culture
This a variant of dry skinIt is usually asymptomaticAppears worse in summer, better during school yearTreatment is sunscreen and moisturizer
KERATOSIS PILARIS
Very common!!
Become more extensive in drier climate.
Individual lesions represent plugs of stratum corneum in individual follicular openings
ie: Skin Trash
Moisturizer with urea of lactic, salycylic acid May help but is not curative.
ID REACTI
ON
Autose
nsitiz
atio
n Der
mat
itis
auto
ecze
mat
izat
ion
Hypopigmented thickened papules often on elbows , knees
Can be eczematous and very itchy
-found in up to 50% of patients with nickel dermatitis
-nearly always symmetrical
-may also be seen in response to infectious agents, particularly in bacterial and dermatophyte infections.
- In the case of tinea capitis the id reaction is usually seen on the head and neck and is often after initial of oral antifungal agent and is erroneously diagnosed as drug reaction
- Clearance occurs with resolving of the originial cause- nickel avoidance, clearance of tinea, etc.
KNUCKLE PADS
Knuckle pads were medically first described by Garrod in 1893 and are also named Garrod's pads
.
There is no known established, generally successful therapy.
Injection of corticosteroids (triamcinolone) can soften and sometimes even shrink the pads. Radiation therapy has also been reported to be successful in some cases but not consistently.
Knuckle pads can be surgically removed in the case of pain associated with them. .
Aplasia Cutis Congenita
Developmental defect rather than birthmarkOccurs in about 1 in 5000 birthsUlcerated defects may heal with scar.
Although usually benign, the hair collar sign may be associated with other physical anomalies and malformation syndromes.
No specific laboratory tests are required, although a hair collar sign signals the possibility of a CNS malformation and thus may warrant an MRI scan to rule out an underlying pathology
NEVUS SEBACEOUS
Appears at birth as slightly raised yellow orange nevus
At puberty become raised and warty
Basal cell carcinoma and other benign tumors occur in 15-50% of the tumors
Excision recommended prior to puberty.
MASTOCYT
OMA
MASTOCYT
OSIS
URT I C
AR
I A P
I GM
E NT O
SA
Seen in less than 2% of children
Often onset is after 12 months of age
More lesions accumulate slowly with age and lesions do not spontaneously resolve.
System symptoms develop with time in 2% of the children with this form (flushing, tachycardia, hypotension, hepatosplenomegaly
Hereditary Form
URTICARIA PIGMENTOSA
MASTOCYTOMA
Solitary lesionWill not develop more Topical steroids for treatment
of symptoms
Non Hereditary Form of Mastocytosis is much more common
Blotchy macular and nodular pigmented lesions which appear in the first 8 months of life starts with one or 2 and then develop numerous lesions over months.
The hyperpigmented appearance may not appear until 6 months after onset
Darriers sign- stroking the lesion will cause tense edema and redness
Spontaneous clearing by 6 or 7 years of age is usual
Essential that children with any type of Mastocytosis not be given the following medications:
Opiates (codeine, demerol, morphine)Polymixin BAcetylsalicylic Acid
In the case of surgery very important that perioperative medications carefullySelected.
TREATMENT OPTIONS
Nonsedating Antihistamine (zyrtec, Allegra, etc)
Regular daily dosing
Can try every 6 months to stop and if starts flaring then resume medication
Topical Steroids for itching in individual lesions BID
For body Triamcinolone 0.025% or 0.1%
For face/neck/groin/axilla/head Hydrocortisone 2.5% or Desonide 0.05%.
WHICH HEMANGIOMAS WARRANT THIS TREATMENT?
PROPRANOLOL PROTOCOL AT CMC DERMATOLOGY
Prior to initiation of therapy needs :
BP
Pulse
Chest Xray
ECG
Propranolol 1mg/kg/dose administer BID (20mg/5ml solution)
PROPRANOLOL
Propranolol 1mg/kg/dose administer BID 20mg/5ml solution
Taper Schedule:
Days 1-4 0.25mg/kg/dose BID
Days 5-9 0.5mg/kg/dose BID
Days 10-13 0.75mg/kg/dose BID
Day 14 and on 1mg/kg/dose BID
Can also divide the above doses to TID (.025mg/kg x2)
3
FOLLOW UP SCHEDULE
Follow up is weekly x 3,then q2w x 4, then montly. BP q visit.
Infants younger than 3 months should have CBG monitored each visit.
Parents should be instructed how to count pulse and recognize low heart rate
They should watch for somnolence, perioral pallor, cold hands and feet.
Patients must be fed q4h while on this medication due to hypoglycemia possibility
11/17/12 baseline
11/26/12
12/3/12
12/10/12
12/17/13
12/31/13
01/17/13
3/5/13
9/13/13
3/17/14
DERMATOLOGY INFORMATION RESOURCESTextbooks:
Color Textbook of Pediatric Dermatology- Weston, Lane, and Morelli
Pediatric Dermatology- Bernard A Cohen
Great for pictures and information that is clinically helpful.
DermNet NZ. Facts about the skin. www.dermnetnz.org
Skin Advocate App- available for free in app store- has information on parent and patient support organizations and is set up for you to email the address directly to the patient with a share line. (Developed by UTSW Resident and received national award !)
Some things can be fixed and some cannot…..
However we do know that education and information is just as valuable as cures can be.
The goal is always………….
HAPPY PT., HAPPY MOMMA, HAPPY GRANDMA!!