Common Skin Disorders Flashcards

0
Q

Hereditary: either a family or a personal history of asthma, allergic rhinitis, or AD

Infants: cheeks, extensors, trunk
Child: flexors, neck
Adolescent: hands

Dry skin and horny follicular papules

Exacerbated by dry skin, contact sensitivity, stress and anxiety

Topical hydrocortisone or fluocinolone

Moisturizers after the topical steroids

Cloxacillin or Cefalexin for infected lesions

A

ATOPIC DERMATITIS

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1
Q

Lesions are limited to the area of contact the external substance

Poison ivy, nickel, cosmetics, perfume, soap

Form of cell-mediated injury

Management:

  • Keep the area dry
  • Use of mild to moderate topical steroids (HYDROCORTISONE or FLUOCINOLONE)
  • treat superimposed bacterial infection first with either CEFALEXIN or CLOXACILLIN
A

ALLERGIC CONTACT DERMATITIS

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2
Q

Due to strong chemicals that penetrate the epidermal barrier readily, or weaker chemicals that penetrate a faulty epidermal barrier, or substances that remove intracellular lipid

Management:

  • Keep the area dry
  • Use of mild to moderate topical steroids (HYDROCORTISONE or FLUOCINOLONE)
  • treat superimposed bacterial infection first with either CEFALEXIN or CLOXACILLIN
A

IRRITANT CONTACT DERMATITIS

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3
Q

Unknown mechanism: excessive sebum accumulation on scalp, face, midchest, perineum

Greasy scalp (cradle cap), greasy scales in nasolabial folds or eyebrows

Physiologic overproduction of sebum in the 1st 6 months of life

Topical low potency steroids; keratolytic shampoo

A

SEBORRHEIC DERMATITIS

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4
Q

Erosions covered by moist, honey-colored crusts in face, nares, extremities

Bullous- lesion with central moist crust and an outer zone of translucent blister

Staph aureus, group A streptococcus

Depth of invasion is until the upper epidermis

Microscopic breaks in the epidermis like trauma of scratching the skin

CLOXACILLIN or CEFALEXIN with or without MUPIROCIN

A

IMPETIGO

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5
Q

Entire epidermis is involved

Firm, dry, dark crust with surrounding redness and induration

Both impetigo and ecthyma: CLOXACILLIN 50-100mg/kg/day every 6 hours

Good personal hygiene

A

ECTHYMA

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6
Q

Tender, warm, erythematous plaques with ill- defined borders

Regional lymphadenopathy and fever

Preceding puncture wound or other penetrating trauma to the skin is noted

STREP, STAPH, H. INFLUENZAE
- invasion of bacteria into the deep dermis and subcutaneous fat

Management:

  • PENICILLIN 600,000- 1.2 M units/kg/day q 6 hours for streptococci
  • OXACILLIN 100-200 mg/kg/day q 6 hours for staphylococci
  • AMPICILLIN (100-200 mg/kg/day) + Chloramphenicol (50-100 mg/kg/day) for H. Influenzae
  • CEFUROXIME, CEFTRIAXONE, or CEFOTAXIME
A

CELLULITIS

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7
Q

Tender erythematous nodule

Management:

  • CLOXACILLIN or CEFALEXIN
  • I & D
A

Furunculosis

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8
Q

Confluence of several adjacent areas of furuncles producing a tender red tumor

Management:

  • CLOXACILLIN or CEFALEXIN
  • I & D
A

Carbuncle

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9
Q

Long-standing carbuncle that becomes soft and fluctuant

Management:

  • CLOXACILLIN or CEFALEXIN
  • I & D
A

Abscess

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10
Q

S. aureus of phage group II elaborates a staph. exfoliatin A carried via the circulation to the skin —> acts on the cells surface of the epidermal granular cells —> injury results in intraepidermal separation of the cells within the granular layer —> shedding of the entire granular layer and stratum corneum when a minor trauma occurs

Spectrum: from bullous impetigo to generalized involvement

Faint red eruption in face, neck, axilla and groin

Skin rapidly becomes tender with crusting around the mouth, eyes and neck

Mild rubbing of the skin results in epidermal separation leaving a shiny, moist, red surface – (+)Nikolsky sign

OXACILLIN; fluid and electrolyte correction; bland ointments during the desquamation phase

A

STAPHYLOCOCCAL SCALDED SKIN SYNDROME

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11
Q

MALASSEZIA FURFUR invades the stratum corneum which thrives hot, humid climate and colonizes the skin by adolescence

KOH scraping: short curved hyphae and circular spores (“spaghetti and meatballs”)

MICONAZOLE, CLOTRIMAZOLE, or FLUCONAZOLE

SELENIUM SULFIDE 2.5% overnight application once weekly for 4 weeks

A

TINEA VERSICOLOR

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12
Q

Colonization of the oral cavity, GIT, and vagina AOG healthy individuals by Candida albicans is normal

Moisture, warmth, and breaks in the epidermal barrier permit overgrowth and invasion of the epidermis

C. Albicans generates inflammation by activation of the complement system within the skin and attraction of neutrophils to skin sites –> keratolytic proteases allow them to penetrate the epidermal barrier

Neonates & infants: white plaques on a red base (thrush) in the buccal mucosa; intertrigenous areas (beefy erythema with elevated margins and satellite red plaques) like inframammary, Axillary, neck & inguinal body folds

Adolescent females: whitish plaques on red mucous membrane of vulvovaginal areas with cheesy vaginal discharge

Oral thrush: oral NYSTATIN 4x/day for 5 days

Skin: KETOCONAZOLE, MICONAZOLE, CLOTRIMAZOLE

A

CANDIDIASIS

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13
Q

Due to Sarcoptes scabiei where the female mite remains in the stratum corneum — deposits eggs and dies after 30-40 days

Transmission of scabies requires human contact and itching - occurs 3 weeks after infestation

Pruritic papules on the abdomen, dorsa of he hands, flexors, periaxilla, genitalia, interdigits

Secondary impetigo is common

Brown crusted nodules on the trunk: S-shaped burrows are diagnostics

Permethrin 5% for 8-14 hours has a 98% cure rate

Lindane lotion one 6-hour application

Itching may persist for 7-10 days after successful therapy

A

SCABIES

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14
Q

Benign tumors of capillary endothelium

Pale white to gray-blue macule; telangiectatic; papule form

Growth phase followed by regression in the 2nd year of life

By 9 years old, 90% have reached maximal progression

Oral steroids at 2mg/kg

Platelet trapping with consumptive coagulopathy (KASABACH-MERRITT SYNDROME); systemic steroids and fresh frozen plasma; interferon; pulsed dye laser if ulcerated

A

HEMANGIOMA

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15
Q

Due to poxvirus that induces epidermal cell proliferation

Type 1 - extremities, head & neck

Types 2 & 3 - genital lesions

Incubation period of 2-7 weeks and thchild is contagious as long as activ lesions are present

White or yellow 1-6mm discrete papules with a central umbilication

Some may extrude keratinous contents from the center

Around the eyes, axilla, proximal extremities

Removal with a sharp curette

Recurrence are common

A

MOLLUSCUM CONTAGIOSUM

16
Q

Type 1 or juvenile onset - AD

HLA-Cw6 & HLA-DR7 are increased

Inflammation with epidermal proliferation

Clinical dx: thick silvery scales, nail involvement and isomorphic phenomenon (lesions develop in sites of skin trauma several days after the event)

Scalp, ears, eyebrows, elbows, knees, gluteal crease, genitalia & nails

Itching is a variable feature

Management:

  • Therapy aims to retard epidermal proliferation
  • Topical steroids - 2-3 weeks temporary improvement followed by phototherapy (UVL)
  • salicylic acid 3% for the scalp
A

PSORIASIS

17
Q

Due to allergic reactions to drugs, climate, food, insect bites, etc

Histamine directly released from cutaneous mast cells

Red, raised, irregular border, pruritic wheals scattered over the body which are evanescent - URTICARIA

subcutaneous lesions are called ANGIOEDEMA

A

Hypersensitivity Reaction

18
Q

Oral antihistamines

Avoid the offending substance

Diphenhydramine 1mg/kg (max 50mg) IM

A

Urticaria

19
Q

Due to a HSV specific host respond to HSV antigens expressed in keratinocytes within the target lesion

Oval or round, fixed, red skin lesions with dusky central zone - target or iris lesion

Recurrent; dorsal surface of hands and extensors, palms & soles

Absent systemic symptoms and signs

Wet compress and oral antihistamines

A

ERYTHEMA MULTIFORME

20
Q

Due to genetic susceptibility to injury – toxic effect on keratinocytes and mucosal epithelial cells

Related to drug infections with NSAIDs, sulfonamide and anticonvulsants

Serious and life-threatening

Large areas of epithelial necrosis

Prodrome of fever, headache, sore throat, malaise

Severe mucosal involvement with extensive mucosal necrosis and always involves at least 2 mucosal surfaces (oral, genital, urethral, GIT, lower respiratory tract)

Rapid progression from central blisters to severe epidermal necrosis with loss of epidermis leaving a denuded skin — hemorrhagic crusts on the lips

Management:

  • Discontinue the offending drug
  • fluid and electrolyte replacement; prevention of secondary bacterial infection; ophthalmologic consultation
  • no evidence of effect of systemic steroids
A

STEVEN JOHNSON SYNDROME