Pediatric Dermatology Flashcards

1
Q
  • causes orolabial, genital and congential infections
  • transmission occurs during asymptomatic and symptomatic periods of viral shedding
  • majority of seropositive individuals report having no history of genital herpes infection
  • prodrome of tender LAD, malaise, fever, localized pain, tenderness and burning
  • symptoms appear 3 to 7 days after exposure
  • usually presents as gingivostomatitis in children or pharyngitis and a mononucleosis-like syndrome in YA
A

Herpes simplex virus

HSV 1

  • primarily associated with oral and labial lesions
  • largely a childhood disease of oral mucosa, pharynx, lips and occasionally eyes

HSV 2

  • primarily associated with anogenital lesions
  • commonly spread via a sexual contact or neonates by passage through an infected birth canal
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2
Q
  • ooccurs in atopic dermatitis
  • often acute worsening of the eczema (widespread eruption of monomorphic vessels and erosions, especially in areas of active eczema
  • often with fever, adenopathy, irritability
  • treatment: IV antivirals typically
A

HSV: Eczema herpeticum

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3
Q

HSV treatment

A

Primary Orolabial

  • self-limited but may treat if poor intake and dehydration
  • most effective when started early (within 72 hrs of onset)
  • acyclovir, valacyclovir for recurrent treatment
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4
Q
  • prodrome of mild fever, malaise and myalgia
  • pruitic, erythematous macules and papules–> vesicles surrounded by red halos (dew drops on a rose petal–> pustules and crusts
  • starts on the scalp and face then spread to the trunk and extremities. often involvement of the oral mucosa
  • heals within 7 to 10 days
  • lesions in all stages of development is the hallmark
  • usually benign and self limited
A

Varicella

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5
Q

complications of varicella?

A
  • secondary bacterial infection with subsequent scarring is the most common complication
  • reye’s syndrome, encephalitis and acute cerebellar ataxia are rare
  • primary varicella in adults often more severe with more complications
  • Congenital: low birthweight, cicatrical lesions, ocular abnormalities, cortical atrophy, psychomotor retardation and hypoplastic limbs
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6
Q
  • 3 c’s: cough, coryza and conjunctivitis
  • prodrome of fever, cough, nasal congestion and rhinoconjunctivitis and koplik spots (gray- white papules on the buccal mucosa
  • erythematous macules and papules begin on the forehead, hairline and behind the ears then spreads downward onto the trunk
  • on 5th day exanthem starts to fade in the same order that it happened

tx: supportive, two dose vaccine

A

measles

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7
Q

complications of measles?

A
  • otitis, pneumonia, gastroenteritis, enecephalitis and myocarditis
  • subacute sclerosing panencephalitis (delayed neurodegenerative disorder may occur many years later)
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8
Q
  • Aka Erythema infectiousum
  • caused by parvovirus B19, a single stranded DNA virus
  • transmission by respiratory secretions, blood products and vertical
  • peak incidence during winter and spring
  • most common in school-aged children
  • may begin with mild prodrome of headaches, fever, chills or respiratory symptoms
  • 2-3 days after prodrome, bright red macular erythema of the cheeks (slapped cheeks) spares nasal bridge and perioral areas
  • 1-4 days after facial rash, erythematous macules and papules which progress to a lacy, reticulate pattern
A

fifth disease

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9
Q
  • Aka exanthem subitum or sixth disease
  • causes by human herpes virus (HHV) 6 or 7
  • transmission: saliva, horizontal
  • most common in ages 6mon-3yrs
  • peak incidence is 6-7 months
  • high fever in infant who otherwise appears well
  • diffuse rash appears after abrupt defervescence –> rose-pink macules and papules on the trunk, neck, proximal extremities and ocassionally face

tx: supportive, antipyretics

A

Roseola

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10
Q
  • caused most frequently by cosackie A16 (enterovirus)
  • peak incidence is later summer and fall
  • incubation is 4-6 days
  • 1-2 day prodrome of fever, malaise, sore throat
  • gray oral vesicles on red or flesh colored base on hands, feet (can also occur on buttocks, trunk face, and extremities: usually burn or pruritic)
  • Vesicles rapidly ulcerate in mouth to leave erosions on tongue, buccal mucosa, posterior pharynx
  • tx: supportive; usually clears in < 1 week
A

Hand-foot-mouth diseae

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11
Q

types of diaper dermatitis?

A
  • infant dermatitis
  • candidiasis
  • seborrheic dermatitis
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12
Q
  • due to moisture, feces, urine, bacteria,
  • erythematous patches +/-blisters and erosions
  • buttocks, vulva, perianal area, lower abdomen and proximal thighs
  • spares skin folds
A

irritant contact dermatitis

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13
Q
  • c.albicans
  • beefy red erythema
  • erythematous papules that involve skin folds, with pinpoint pustulovesicular satellite lesions
  • atopic dermatitis typically spares the groin and diaper area during infancy due to increased hydration/moisture
A

candidiasis

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14
Q
  • salmon colored greasy plaques with yellowish scale
  • hypersensitivity to overgrowth of normal lipophilic yeast
  • areas with the highest concentration of sebaceous glands- namely the scalp, face, postauricular, presternal and intertriginous areas
  • erythematous, yellowish greasy scale or crusting eruption
  • “cradle cap”
  • tx: self limited- ketoconazole shampoo, topical corticosteroid to treat the infammation
A

seborrheic dermatitis

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15
Q
  • most commonly due to C. albicans followed by C. Trpicalis
  • tongue, soft and hard palate and buccal and gingival mucosae
  • white, friable patches or plaques overlying reddened mucosa
  • predisposing factors in children and adults (diabetes mellitus, xerostomia, occlusion, hyperhidrosis, the use of corticosteroids and broad spectrum antibitotics and immunosuppresion, including HIV infection
A

Thrush

DX: clinical, KOH shows budding yeast, fungal culture

tx: nystatin oral suspension

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16
Q
  • most common benign soft tissue tumor of infancy
  • more common in white infants
  • most become apparent first 2-3 weeks of life
  • if noted at birth, can be fully formed or more commonly show a precursor lesions
  • three phases: period of growth (proliferative phase), period stability (plateau phase), period of regression(involution phase)
A

Hemangioma of infancy

17
Q
  • constellation of clinical findings associated with extensive infantile hemangiomas
  • majority female
  • facial hemangiomas are usually large and sefmental
  • hemangiomas may also occur in other non-facial locations inluding upper torso and arms
  • screening with MRI of brain, echocardiography, opthalmologic examination and close neurologic and head circumference examination
A

PHACES syndrome

18
Q

Treatment of hemangioma of infancy

A
  • active non-intervention
  • local wound care for ulcerated hemangiomas
  • current standard of care: oral beta-blocker propranolol
  • topical beta-blocker timolol for smaller, localized and/or superficial
  • topical or intralesional corticosteroids for localized superficial lesions
  • oral corticosteroids
19
Q
  • Isolated or multiple lesions
  • multiple lesions sometimes a marker for multi system disease in various syndromes
  • may be present at birth, but usually become obvious during early childhood
  • located anywhere on the body, except mucous membranes
  • color of coffee with milk, light to dark brown
A

Cafe au lait

20
Q
  • Triad: cafe au lait macules, polyostotic fibrous dysplasia and precocious puberty
  • cafe au lait macules typically in fewer in number, larger, darker and may follow blaschko’s lines
  • predelection for areas with bony prominences: forehead, nuchal area, thorax, sacrum and buttocks
  • commonly unilateral
  • can be indistinguishable from cafe au lait macules in neurofibromatosis - axillary freckling does not occur
A

McCune-Albright syndrome

21
Q

diagnostic criteria for neurofibromatosis 1

A
  • 6 or more cafe au lait macules measuring >5mm before puberty and > 15mm in post pubertal (usually in first year of life)
  • freckling of axillary and or inguinal areas
  • 2 or more neurofibromas or 1 plexiform neurofibroma (usually at puberty)
  • 2 or more lisch nodules (iris hamartomas)
  • optic nerve glioma
  • skeletal dysplasia; (i.e tibial or sphenoid wing dysplasia
  • 1st degree relative with NF1