Psoriasis vulgaris

Last Updated: 2025-10-10

Author(s): Navarini A.

ICD11: EA90.0

Psoriasis, Psori

A chronic, immune-mediated, systemic inflammatory disease characterized by clearly defined erythematous plaques with silvery-white scales, variable nail and joint involvement, and a wide range of cardiometabolic and psychosocial comorbidities.

  • Global prevalence ≈ 2–3%; in Switzerland ≈ 2–3%.
  • Bimodal age of onset: first peak at 15–35 years (type I) and second peak at 55–60 years (type II).
  • Equal gender ratio; positive family history in 30–40% of cases with early onset.
  • According to age at onset:
    • Type I (< 40 years, often HLA-C*06:02-positive, more severe).
    • Type II (> 40 years, milder, less familial).
  • By morphology:
    • Psoriasis vulgaris (plaque type, > 90%).
    • Guttate, pustular (localized/generalized), erythrodermic, inverse, palmoplantar, cranioscapular, nail, psoriatic arthritis.
  • Genetics: Polygenic; strongest association with HLA-C*06:02 (PSORS1, 6p21.3).
  • Triggers: streptococcal pharyngitis, lithium, β-blockers, antimalarial drugs, NSAIDs, stress, alcohol, smoking, skin trauma (Köbner phenomenon).
  • Immunology: Activation of the IL-23/IL-17 axis; key role for dendritic cells, Th17 cells, γδ T cells, tissue-resident memory T cells, and neutrophilic Munro microabscesses.
  • Skin: Sharply defined erythematous plaques with silvery scales; scalp, extensor surfaces of elbows/knees, sacrum, genitals, palms, soles of feet.
  • Nails: Pitting, onycholysis, oil drop sign.
  • Joints: Psoriatic arthritis in 20–30%; dactylitis, enthesitis, axial disease.
  • Signs: Köbner phenomenon, Auspitz sign, candle wax sign. Pruritus in ≈ 50%.
  • Severe variants: erythroderma, generalized pustular psoriasis.
  • Typical clinical picture ± family history.
  • Screening: PEST questionnaire for arthritis.
  • Biopsy: acanthosis, parakeratosis, loss of granular layer, Munro microabscesses, Kogoj spongiform pustules, dilated papillary capillaries.
  • Laboratory: Baseline and control values for systemic therapy (complete blood count, liver values, kidney function, lipids).
  • Differential diagnosis: Atopic dermatitis, seborrheic dermatitis, nummular eczema, pityriasis rubra pilaris, mycosis fungoides, secondary syphilis, tinea corporis.
  • Adults: The scalp, extensor surfaces, and lumbosacral region are most commonly affected.
  • Children: More common on the face and flexor surfaces.
  • Medical history: Recurrent flare-ups, worsening in winter, improvement with sunlight, identifiable triggers, positive family history.

Regular psoriasiform hyperplasia with elongated retespitzen; confluent parakeratosis; absence of granular layer; neutrophils in the stratum corneum and spinous layer; dilated, tortuous papillary capillaries; perivascular lymphocytic infiltrates.

  • Psoriatic arthritis (7–48%).
  • Cardiovascular disease, metabolic syndrome, obesity, dyslipidemia.
  • Depression/anxiety, NAFLD, IBD (Crohn's disease > ulcerative colitis), uveitis.
  • Chronic recurrent course; lifelong disease.
  • Early, sustained control improves quality of life and reduces the risk of comorbidities.
  • Modern biologics achieve PASI 90/100 in >70% of patients.
  • Avoidance of known triggers (infections, medications, alcohol, smoking, stress).
  • Daily use of skin care products; weight control; regular exercise; smoking cessation.
  • Screening for psoriatic arthritis and cardiometabolic diseases at every doctor's visit.

1. General measures

  • Intensive patient education; psychosocial support; consistent emollient therapy.

 

2. Topical therapy

  • First-line therapy: calcipotriol + betamethasone dipropionate foam (Enstilar®) once daily for 4–8 weeks.
  • Class II–IV corticosteroids (locally adapted).
  • Calcineurin inhibitors (Protopic® 0.1% ointment) for the face, flexural areas, inverse disease.

 

3. Phototherapy

  • Narrowband UVB 311 nm (2–3 times per week) first choice; PUVA for refractory conditions or scalp conditions.

 

4. Systemic small molecules

  • Methotrexate s.c. 10–15 mg/week + folic acid 5 mg the following day.
  • Dimethyl fumarate (Skilarence®) – titrate to 240 mg twice daily; monitor lymphocytes.
  • Apremilast (Otezla®) 30 mg twice daily (oral PDE-4 inhibitor).

 

5. Biologics

  • IL-23 inhibitors:
    • Risankizumab 150 mg s.c. in weeks 0 and 4, then every 12 weeks.
    • Guselkumab 100 mg s.c. in weeks 0, 4, then every 8 weeks.
    • Tildrakizumab 100 mg s.c. in weeks 0, 4, then every 12 weeks.
  • IL-17 inhibitors:
    • Secukinumab 300 mg s.c. in weeks 0, 1, 2, 3, 4, then every 4 weeks.
    • Ixekizumab 160 mg in week 0, then 80 mg every 2 weeks until week 12, then every 4 weeks.
    • Bimekizumab 320 mg every 4 weeks until week 16, then every 8 weeks.
  • IL-12/23 inhibitor:
    • Ustekinumab 45 mg (< 100 kg) or 90 mg (> 100 kg) s.c. in weeks 0, 4, then every 12 weeks.
  • TNF-α inhibitors:
    • Adalimumab 80 mg in week 0, then 40 mg every two weeks.
    • Certolizumab pegol 400 mg in weeks 0, 2, 4, then 200 mg every 2 weeks (safe during pregnancy).

 

6. Psychological measures and lifestyle changes

  • Cognitive behavioral therapy, stress management programs, weight loss support.
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  5. Armstrong AW, Husted JD, et al. Risk of depression among biologics users: real-world data. JAMA Dermatol. 2023;159:223-231. PMID: 36688542
  6. Federal Office of Public Health. National Strategy on Noncommunicable Diseases 2023–2029. Bern; 2023.
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  8. Schlapbach C, Yawalkar N. IL-23/IL-17 axis in Swiss practice. Ther Umsch. 2023;80:135-142. PMID: 37015678
  9. European Academy of Dermatology and Venereology. EuroGuiDerm Clinical Practice Guideline – Psoriasis 2024 Update.
  10. StatPearls [Internet]. Psoriasis – Etiology, Pathophysiology, Treatment. Treasure Island (FL): StatPearls Publishing; April 3, 2023. Available at: https://www.ncbi.nlm.nih.gov/books/NBK448194/