Dermatology
Showing 22 of 22 topics
A
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Identify and avoid allergens, use topical corticosteroid for localized disease, consider short systemic steroid burst for severe widespread involvement, and refer for patch testing when recurrent.
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Autoimmune non‑scarring hair loss. Treat limited disease with intralesional steroids; consider topical immunotherapy and emerging JAK inhibitors for extensive disease; screen for associated autoimmune disease selectively.
B
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Tense pruritic bullae in older adults; avoid debridement, treat secondary infection, start high potency topical corticosteroid for localized disease or systemic prednisone when extensive, and ensure dermatology follow up.
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Autoimmune subepidermal blistering in older adults; tense pruritic bullae. Diagnose with biopsy and DIF (linear IgG/C3 at BMZ). Treat with potent topical steroids or systemic therapy; manage pruritus and infections.
D
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Inducible urticarias (dermatographism, cholinergic, cold, pressure). Identify triggers and use high‑dose second‑generation antihistamines; escalate to omalizumab or cyclosporine for refractory cases; educate on anaphylaxis risk in cold urticaria.
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Recognize rash with facial edema, eosinophilia, and systemic involvement; stop the offending drug, evaluate organs, and give systemic corticosteroid for significant organ disease.
E
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Disseminated HSV in patients with dermatitis is a dermatologic emergency; start systemic acyclovir, obtain viral testing, evaluate for bacterial superinfection, and admit if severe.
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Diffuse erythema and scaling can cause fluid, protein, and heat loss; stabilize, identify the cause, and prevent complications.
H
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Start oral antiviral within 72 hours of rash onset or later if new lesions are appearing or eye or ear is involved; provide pain control and ophthalmology referral for ocular involvement.
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Manage painful nodules and abscesses with analgesia, intralesional steroid, short antibiotic courses when infected, and selective incision and drainage or deroofing.
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Assess androgen excess and rule out serious causes; most cases due to PCOS. Treat with combined oral contraceptives and antiandrogens (spironolactone) with reliable contraception; add cosmetic hair removal methods.
I
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Localized non bullous impetigo is treated with topical therapy, while more widespread disease needs oral antibiotics targeting common pathogens and local resistance patterns.
L
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Inflammatory condition affecting skin, oral/genital mucosa, nails. Diagnose clinically and with biopsy when uncertain; treat with high‑potency topical steroids; systemic therapy for extensive or erosive disease; screen for hepatitis C.
N
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Common nail disorders require etiology‑specific care: avoid moisture/trauma for paronychia; treat infections; manage psoriatic nail disease with topical/systemic therapy; correct underlying causes of onycholysis.
P
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Autoimmune intraepidermal blistering with mucosal involvement. Diagnosis by biopsy showing acantholysis and DIF with intercellular IgG; treat with systemic steroids plus rituximab as first‑line.
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Differentiate phototoxic vs photoallergic reactions and specific photosensitive diseases (LE, PCT). Workup includes detailed drug/sun exposure history and targeted labs. Emphasize broad‑spectrum sun protection and trigger management.
S
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Intense pruritus worse at night with burrows; treat with permethrin 5 percent cream or oral ivermectin when appropriate, treat close contacts, and manage post scabetic itch.
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Severe mucocutaneous reaction requiring immediate cessation of culprit drug, burn-level supportive care, and early transfer to experienced center; consider immunomodulatory therapy per protocol.
T
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Dermatophyte infections: tinea capitis requires systemic therapy; tinea corporis often topical. Diagnose with KOH prep or culture; consider kerion and household transmission.
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Requires systemic antifungal therapy; choose oral griseofulvin or terbinafine based on organism and age, and use antifungal shampoos to reduce transmission.
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Life‑threatening epidermal necrosis usually triggered by medications. Stop culprit drug, admit to burn/ICU, apply SCORTEN for prognosis, and provide meticulous wound, fluid, and infection care. Consider cyclosporine or etanercept in selected cases; IVIG evidence mixed.
V
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Autoimmune depigmentation with loss of melanocytes. Combine topical therapies with NB‑UVB; consider systemic JAK inhibitors in select; address psychosocial impact and sun protection.
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