Skin Disorders

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79 Terms

1
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What is pruritus the most common symptom of?

Patients with dermatologic disorders.

2
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What are the manifestations of pruritus?

Generalized itching; perineal/perianal itching may be from fecal particles, scratching, moisture, corticosteroid/antibiotic therapy, hemorrhoids, fungal/yeast infections, pinworm, or no cause.

3
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What systemic disorders are associated with generalized pruritus?

Allergic reactions, immune disorders, liver disease, kidney disease.

4
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What should be included in assessment of pruritus?

Evaluate skin, bathing/hygiene habits, medications/home remedies, inspect perineal area, determine triggers (heat, alcohol, caffeine, irritants, clothing).

5
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How is pruritus managed?

Reinforce therapeutic regimen, educate on self-care (tepid baths, gentle drying, lubrication, avoid heat/alcohol/hot foods, avoid bubble baths/detergent soaps, wear cotton/natural fabrics).

6
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What medications are used for pruritus?

Menthol creams, zinc oxide calamine, anti-itch creams (crotamiton, capsaicin), mild steroid ointments (hydrocortisone), antihistamines, lightweight lotions.

7
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What is recommended perineal/perianal care for pruritus?

Rinse with lukewarm water, blot dry, use premoistened tissues, maintain fiber intake.

8
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What is dermatitis?

Inflammation/irritation of skin, noncontagious.

9
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What are risk factors for dermatitis?

Contact with allergens, stress, family history/genetics, sometimes unknown.

10
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What are the signs and symptoms of dermatitis?

Itchy, painful skin; dry, cracked, or scaly skin; rash with swelling and color variation; blisters that may ooze or crust.

11
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What are the three types of dermatitis?

Nonspecific eczematous (dry/moist, itchy, bilateral), contact (site-specific inflammation, acute vs chronic changes), atopic (chronic allergic, red papules, lichenification, common on hands, elbows, knees, face, neck).

12
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What is assessed in contact dermatitis?

History (onset, exposures), physical exam (location, distribution), patch testing, environmental exposure.

13
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What is assessed in atopic dermatitis?

History (triggers, atopic conditions), physical exam (lesion morphology/distribution), labs/biopsy if needed.

14
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How is dermatitis managed?

Identify/avoid cause, prevent scratching, use fragrance-free products, wash skin after irritants, cool compresses, oatmeal baths.

15
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What specific management is used for contact dermatitis?

Avoid irritant, acute cool compresses (Burow solution), topical/systemic corticosteroids, oral antihistamines, hydrophilic cream, antibiotics if infected.

16
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What specific management is used for atopic dermatitis?

Avoid triggers, hydrate skin with emollients, topical corticosteroids, topical calcineurin inhibitors, short systemic steroids, dupilumab, antibiotics for infection, antihistamines for itching.

17
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What medications are used for dermatitis?

Steroids (hydrocortisone, betamethasone, prednisone), antihistamines (diphenhydramine), topical immunosuppressants (tacrolimus).

18
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What causes impetigo?

Staphylococcus aureus, Streptococcus pyogenes, MRSA.

19
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What are manifestations of impetigo?

Small red macules → vesicles → honey-yellow crusts, usually on face, hands, neck, extremities; contagious.

20
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How is impetigo assessed?

History of skin trauma/hygiene, physical exam of lesions.

21
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How is impetigo managed?

Topical antibiotics (mupirocin, retapamulin), systemic antibiotics if widespread, wash/soak lesions, monitor complications.

22
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What patient education is given for impetigo?

Bathe daily with bactericidal soap, hand hygiene, separate towels/washcloths, avoid contact until healed.

23
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What causes folliculitis, furuncles, carbuncles?

Staphylococcus aureus.

24
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What are manifestations?

Folliculitis = pustules at follicles; furuncle = deep boil, painful/tender; carbuncle = multiple furuncles, systemic symptoms possible.

25
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How are they assessed?

Exam lesions, risk factors (shaving, clothing, diabetes, immunocompromise).

26
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How are they managed?

Warm compresses, systemic antibiotics (based on culture, MRSA coverage), incision/drainage if needed.

27
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What education is given for furuncles/carbuncles?

Maintain hygiene, avoid squeezing, wash linens, seek care for facial boils.

28
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What causes herpes zoster?

Reactivation of varicella-zoster virus.

29
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What are manifestations of herpes zoster?

Preeruptive pain/itching, acute unilateral vesicular rash with pain, postherpetic neuralgia, ophthalmic involvement.

30
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How is herpes zoster assessed?

History of chickenpox, exam of dermatomal rash.

31
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How is herpes zoster managed?

Antivirals (acyclovir, valacyclovir, famciclovir), pain meds, pregabalin/gabapentin for neuralgia, ophthalmology referral if ocular.

32
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What patient education is given for herpes zoster?

Take antivirals as prescribed, hygiene, calamine/Burow's for comfort, rest.

33
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What causes herpes simplex?

HSV-1 (oral), HSV-2 (genital).

34
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What are manifestations of herpes simplex?

Painful vesicles, erythema, ulcers, recurrent outbreaks.

35
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How is it assessed?

History of outbreaks, lesion exam.

36
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How is it managed?

Antivirals (acyclovir, valacyclovir, famciclovir).

37
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What education is given for herpes simplex?

Avoid direct contact, good hygiene, medication adherence.

38
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What causes fungal infections of skin?

Dermatophytes (Trichophyton, Microsporum, Epidermophyton).

39
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What are common types of tinea?

Pedis (athlete's foot), corporis (ringworm), capitis (scalp), cruris (jock itch), unguium (nails).

40
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How are fungal infections assessed?

Inspect lesions, KOH prep, culture if needed.

41
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How are fungal infections managed?

Topical antifungals (clotrimazole, terbinafine, ketoconazole); oral antifungals for severe/nail/scalp infections.

42
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What patient education is given for fungal infections?

Keep area clean/dry, don't share items, complete meds, wear breathable clothing.

43
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What is pediculosis?

Infestation by lice.

44
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What are the types of pediculosis?

Capitis (head), corporis (body), pubis (crabs).

45
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What is scabies?

Infestation by mite Sarcoptes scabiei.

46
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What are manifestations of scabies?

Intense itching (worse at night), burrows, vesicles/papules, crusts, crusted scabies in elderly.

47
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How are pediculosis and scabies assessed?

Look for nits/lice/burrows, secondary infection, microscopic scraping.

48
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How are they managed?

Permethrin or pyrethrin shampoos/lotions, treat all contacts, wash clothing/bedding hot, antibiotics if secondary infection, symptomatic antihistamines/corticosteroids.

49
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What patient education is given for lice/scabies?

Not a sign of poor hygiene, avoid sharing items, treat all contacts, wash/disinfect fabrics, avoid repeat scabicide.

50
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What is psoriasis?

Chronic autoimmune inflammatory skin disease with rapid keratinocyte turnover.

51
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What are risk factors for psoriasis?

Obesity, lithium, beta-blockers, hormones, infections, stress, trauma, cold weather.

52
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What are common sites of psoriasis?

Elbows, knees, scalp, sacrum, extremities, joints.

53
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What are manifestations of psoriasis?

Red plaques with silvery scales, Auspitz sign, nail pitting, arthritis, emotional distress.

54
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How is psoriasis classified by BSA?

Mild <5%, moderate 5-10%, severe >10%.

55
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How is psoriasis managed?

Topicals (steroids, vitamin D analogs, retinoids, tar), phototherapy, systemic (methotrexate, cyclosporine, biologics), adjunctive emollients.

56
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What education is given for psoriasis?

Maintain skin care, avoid scratching, warm water baths, moisturize, know triggers, adhere to therapy, support groups.

57
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What are blistering diseases caused by?

Autoimmune IgG/IgA reactions, infections, burns, contact reactions.

58
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What is the pathophysiology of blistering diseases?

Autoantibodies attack skin antigens → epidermal separation (acantholysis) → bullae.

59
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What are key blistering disorders?

Pemphigus vulgaris (IgG, mucous membranes, Nikolsky sign), bullous pemphigoid (tense bullae), dermatitis herpetiformis (IgA, gluten sensitivity).

60
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What complications can occur in blistering diseases?

Secondary infection, sepsis, fluid/electrolyte imbalance, hypovolemia.

61
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How are blistering diseases managed?

Corticosteroids, immunosuppressants, biologics, dapsone + gluten-free diet, supportive care (oral/skin, infection prevention, pain control, nutrition).

62
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What education is given for blistering diseases?

Long-term management, infection prevention, oral hygiene, diet (gluten-free if DH), avoid scratching, monitor for complications, emotional support.

63
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What is Stevens-Johnson syndrome/TEN?

Severe skin reaction often drug-induced, with epidermal sloughing.

64
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What are manifestations?

Widespread erythema, blisters, mucosal erosions, pain, fever, respiratory risk, ocular damage.

65
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How is it managed?

Stop causative drug, burn-unit level care, wound/oral care, IV fluids, prevent hypothermia, pain control, monitor for infection/sepsis, possible IVIG/cyclosporine.

66
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What education is given for SJS/TEN?

Wound/eye/oral care, infection signs, nutrition, pain control, psychosocial support, rehab follow-up.

67
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What are the main types of skin cancer?

Basal cell carcinoma, squamous cell carcinoma, melanoma.

68
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What are key features of basal cell carcinoma?

Waxy nodule with rolled border, may crust, rarely lethal, recurrence common.

69
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What are key features of squamous cell carcinoma?

Rough, thick, scaly tumor, 4-8% metastasis, \~4000 deaths/year.

70
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What are key features of melanoma?

Most lethal, irregular nevus with color changes, rapid growth/bleeding/ulceration, more common in women (legs) and men (head/neck/trunk).

71
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What are the ABCDEs of melanoma?

Asymmetry, border irregularity, color variation, diameter >6 mm, evolving.

72
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What are risk factors for skin cancer?

Sun exposure, tanning beds, burns, family history, age, smoking, immunosuppression, chemicals.

73
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How is skin cancer managed?

Early excision, wide excision, lymph node biopsy, targeted therapy (BRAF/MEK), checkpoint inhibitors, radiation, topical chemo.

74
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What education is given for skin cancer?

Sun safety, self-exam, ABCDEs, wound care, recurrence monitoring, psychological support.

75
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What is Kaposi sarcoma?

Malignancy of endothelial cells lining blood vessels.

76
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What are manifestations of Kaposi sarcoma?

Reddish-purple to dark blue lesions on skin, oral cavity, GI, lungs.

77
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What are subtypes of Kaposi sarcoma?

Classic (older Mediterranean/Jewish men), endemic (African), iatrogenic (immunosuppression), AIDS-related (aggressive, visceral involvement).

78
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What are risk factors for Kaposi sarcoma?

Older Mediterranean/Jewish men, African origin, immunosuppression, HIV/AIDS.

79
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How is Kaposi sarcoma managed?

Classic = monitor/local, endemic = local/systemic if severe, iatrogenic = reduce immunosuppression, AIDS-related = ART + local/systemic.