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- A chronic, inflammatory disorder most commonly characterized by cutaneous erythematous plaques with silvery scale. It is a complex immune-mediated disorder that results from a polygenic predisposition in the setting of environmental triggers. It is associated with flares related to systemic, psychological, infectious, and environmental factors; skin disease with multiple different phenotypic variations and degrees of severity
- Clinical phenotypes
- Plaque (vulgaris): most common variant (~80% of cases); well-demarcated, red plaques with thick, silvery scale; symmetrically distributed most commonly on the scalp, extensor surfaces of extremities, and trunk
- Guttate: <2% of psoriasis patients, usually in patients <30 years of age; presents abruptly with 1- to 10-mm droplet-shaped pink erythematous papules with fine scale over trunk and extremities; often preceded by group A β-hemolytic streptococcal infection 2 to 3 weeks prior
- Inverse: affects intertriginous areas and flexural surfaces; pink-to-red plaques with minimal scale; absence of satellite pustules distinguishes it from candidiasis although may coexist.
- Erythrodermic: generalized erythema and scaling, affecting 90% of body surface area (BSA) or more; associated with desquamation; hair loss; nail dystrophy; and systemic symptoms such as fever, chills, malaise, and/or high-output cardiac failure; usually requires hospital admission for management of dehydration, electrolyte abnormalities, and high risk of infection
- Pustular: sterile pustules; several forms including generalized pustular psoriasis, localized pustular psoriasis, and impetigo herpetiformis (in pregnancy); generalized type can result in life-threatening bacterial superinfections, sepsis, and dehydration if left untreated.
- Nail disease: pitting, oil spots, and onycholysis; nails involved in up to 50% of patients with psoriasis with lifetime incidence of 80–90%; increased association with psoriatic arthritis
- Psoriatic arthritis: 5–30% of patients; most commonly asymmetrical oligoarthritis involving the hands and feet
Predominant sex: male = female; predominant age: two peaks in incidence between the ages of 20 to 30 years and 50 to 60 years
- 2–4.7%—similar prevalence in all races
- ~80% of patients have mild to moderate disease (1).
Etiology and Pathophysiology
Psoriasis is a complex immune-mediated disorder with interactions between dendritic cells, T lymphocytes, neutrophils, and keratinocytes. It is considered a TH1- and TH17-driven disease with numerous cytokines including TNF-α, interferon-γ, IL-12, IL-17, and IL-23 playing pathogenic roles resulting in an inflammatory, hyperproliferative state.
- Genetic predisposition (polygenic)
- 40% have psoriasis in a first-degree relative.
- Multiple susceptibility loci contain genes involved in immune system regulation (e.g., psoriasis susceptibility [PSORS1] locus on chromosome 6p21; polymorphisms in the IL-12/IL-13 receptor, the p40 subunit of IL-12 and IL-23, and the p19 subunit of IL-12) (2).
- HLA-Cw6 is most strongly correlated with early onset psoriasis.
- Family history
- Obesity (may contribute to more severe disease)
- Local trauma; local irritation (Koebner phenomenon)
- HIV; streptococcal infection
- Mental stress (exacerbation)
- Medications (lithium, antimalarials, β-blockers, interferon, withdrawal of steroids)
Avoid triggers, including trauma, sunburns, smoking, and exposure to certain medications (as mentioned earlier), alcohol, and stress; weight loss if obese
Commonly Associated Conditions
- Psoriatic arthritis
- Seborrheic dermatitis
- Obesity, metabolic syndrome, diabetes, CKD
- Cardiovascular disease; atherosclerotic disease
- Nonalcoholic fatty liver disease (NAFLD)
- Autoimmune: Crohn disease, ankylosing spondylitis
- Psychiatric/psychological: depression, suicide, emotional burden/anxiety, alcohol abuse
- Malignancy: nonmelanoma skin cancer with psoralen-UVA (PUVA) therapy