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31 Cards in this Set
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stages and tx of Hemangiomas -
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- rapidly grow 6-9 mo age;
50% gone by 5 yo; 90% by 9 --oral steroids (2-4 mg/k/day) x 3- 6 wks for vital areas( eye, nose lips, ear, airway) -INVF alpha for recalcitrant cases -propanolol if CS fail; |
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Periobital hemangiomas ~ complx
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~ amblyobia due to visual obstruction or astigmatism;
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Tufted angiomas, kaposiform hemangioendoetheliomas
-rapidly increase in size w/ platelet trapping, consumptive coagulapthy, micronagiopathic anemia ? tx and dx? |
Kassabach Merit
TX: supperitve, steroids, INF, vincritsine |
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Beard hemangiomas ~ what?
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~ upper airway hemangiomas; symptomatic b/w 6-12 wks; **recurrent stridor
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PHACES syndrome: name?
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Posterior fossa brain malformations, Hemangiomas-large plaque like facial, areterial anomlies, cardiac defects, eye abnl, sternal clefting
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Lumbosacral hemangiomas ~ what?
Liver hemangiomas~? |
~ tethered cords, lipomeningoceles
Liver hemang-~ HM, CHF, anemia, occasional thrombocytopenia |
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Hypothryoridsm ~? hemangioma
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~liver, large segmental hemangiomas
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Salmon patches (nevus simplex, vascular stain) - occur mostly where, ? fade; whats tx?
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70 % NB on eyelids, glabella, forehead, neck nape: face lesions fade by 6-12 mo; NO TX needed
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Present at birth, macular pink –red in color; U/L, segmental, darker w/ cobblestone surface w/ time
-Tx |
POrt wine stain;
tx: : vascular specific pulsed dye laser |
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PWS of forehead, upper or lower eyelid ~
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~ ipsilateral glaucoma, ipsilateral leptomeningeal angioma; ~ sz, hemipareisis, MR
-sturge weber |
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PWS ~ limb hypertrophy, lymphedema, venous malformations, GI/bladder angiomas;
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Klippel-Trenaunay; no tx
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Aq’d vascular lesion, most commonly on upper ext or face/ red-brown in color, firm nodule, bleeds easily;
dx and Tx? |
Pyogenic granuloma;
tx: : removal (curettage, lasery, cryotheraphy, surgical excision) |
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Benign melanocytic lesion, firm, dome shaped nodule or papule, red-brown in color; blanches w/ pressure; face or upper ext;
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Spitz nevus
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Skin, CNS, orthopedic manifestation; neurofibromas –after puberty;
-how dx, genetics, chromosome; what |
NF1; AD, chrom 17; ~ pheo, RAS
-dx: need 2/7 for dx (café aulait: >6 after birth > 5 mm; or >15 mm post puberty; lisch nodules (iris hamartomas); neurofibromas, optic nerve glioma; inguinal axillary freckling, bony defects, FH of NF1) |
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> 3 ash leaf spots (hypopigmented skin), periventricular/cortical tubers, sebaceous gland hyperplasia, shagreen patch (cobblesone skin-leathery, orange peel), sub/periungual fibroma, cardiac rhabodmyoma; retinal nodular hamartomas, renal angiomyolipoma; dx and how dx?
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tuberous sclerosis; Need >2 for dx:
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Not present at birth, appears day 1-4, cz?; red macules → yellow, white 1-3 mm papules or pustules w/ red base; spares palms soles, lasts 2-3 wks; Stain: eosinophils
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Erythema Toxicum
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Superficial vesicopustular lesions, PRESENT at BIRTH!!, vesicles rupture w/ first bath (w/in 1-2 days)→scale, no redness, hyperpigmented macules at site of vesicles, persist x months; Blacks > whites; cz ? stain: neutrophils w/o bacteria; vs staph infection – involves hair follicles, stain: PMN + gm + cocci
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-Transient neonatal pustular Melanosis
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Dev d/o of capillaries, veins, localized; ~ gluacomoa, cleft lip, MR, syndactyly, hypothroidism, dystrophic teeth
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Cutis marmorata Telangiectatica Congenita
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Normal reticulated bluish mottling of ext in response to cold
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Cutis marmorata
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Sharply demarcted indurated plaques w/ patchy overlying redness over bony prominences, end of first month of life; due to pressure trauma, asphyxia or hypothermia; resolves spontaneously ~ hypercalcemia
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Subcutaneous fat necrosis
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Not present at birth; seen 2-4 wks age x 1-3 mo; papules, pustules not comedones; no tx; can use benzoyl peroxide or erythromycin topically
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Neonatal acne
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Occurs 3 mo – 4-5 years; often severe, treated like acne in adolescent; ~ more severe acne as an adolescent; consider abnl androgen source if > 1 yr
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Infantile acne
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Mimics neonatal acne; probable inflammatory response to Malasezzia; tx: anti-yeast meds
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Neonatal cephalic pusutulosis
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-2-4 wks life, clears spontaneously by 6-12 mo; recurs as teen ;cz:? greasy, yellow-white scale w/ red macules or papules; scalp, forehead, ears, eyebrows, nasolabial folds, chest, axilla, diaper area; not prurutic
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Seborrheic dermatitis
cz?: Pityrosporum ovale |
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if ~ profuse ear d/c or hi UOP ~ seb derm, whats dx?
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histiocytosis X!!
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whats seb derm tx?
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Tx: mild – none; mineral oil before shampooing, scrubbing w/ brush, mild keratotolytic (zinc, sulfur, salicylic acid); Low potency topical CS cream or ointment ; zinc or selenium shampoos, ketoconazole cream or shampoo – agents that kill P. ovale
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Ring-shaped, red, scaly lesions on face or scalp, red macules, papules, telangicatisias, atrophy;
~ hepatitis, hemolysis, thrombocytopenia or aplastic anemia; No history or prior dx in mom in ½ cases; -cz and dx? how dx ; tx? |
neonatal lupus
-cz: due to maternal AB crossing placenta =Dx: anti Ro- (SSA) and anti-La (SSB); tx: Tx of skin lesions: none, low strength CS, sunblock, resolves by 6-12 mo |
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-clustered or grouped vesicles on red base on but/scalp, not present at birth; wright stain: shows ? ;
-dx and tx? |
neonatal herpes;
-wright stain: multinucleated giant cells, eosinophilic intranuclear inclusions -TX: IV acyclovir; vs Inconteninetia pigmenti – also has vesicles but in linear patern w/o base |
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what allergy ~ Atopic derm?
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Most common: egg, cows milk, soy, wheat, peanuts, fish;
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what ages/stages of location deos atopic derm occur?
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Infants: cheeks, scalp, auricular area; trunk ext –severe;
-spares axillae, diaper area, papules, vesicles; -Child: flexural eareas, wrists, andkles * Adolescents: hands, feet, eyelids w/ some flexural areas; -AA: follicular pattern |
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tx of atopic derm?
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Avoid drying: emollients, mild soap; short lukewarm baths w/ emollient application w/in minutes
-control itching: topical CS once x day > bathing or under emollient to increase penetration!! X 7-14 days -inflammation: CS, topical immunomodulators (tacrolimus) –inhibits calcinuerin w/o systemic SE -tx infection: acyclovir, topical antifungals, antbx; weepy lesions~ bacterial infx; staph aureus colonization -AVOID steroid-antifungal combos; |