Rosacea
Acne rosacea (historical) · phymatous rosacea · ocular rosacea
Rosacea is a chronic inflammatory skin disorder of the central face affecting an estimated 5-10% of UK adults, with peaks in fair-skinned middle-aged and older patients. The 2017 ROSCO phenotype-led classification recognises four overlapping subtypes: erythematotelangiectatic, papulopustular, phymatous and ocular. Phymatous rosacea — particularly rhinophyma — is the principal mimic of basal cell carcinoma of the nasal tip, and chronic actinic damage with sebaceous hyperplasia can overlap clinically. NICE CKS rosacea guidance underpins UK primary-care management.
Subtypes (ROSCO 2017 phenotype-led)
- Erythematotelangiectatic — persistent central facial erythema, flushing, telangiectasia.
- Papulopustular — inflammatory papules / pustules on background erythema; spares perioral skin (cf. perioral dermatitis).
- Phymatous — sebaceous-gland hypertrophy and fibrosis; rhinophyma (nose), gnathophyma (chin), metophyma (forehead), otophyma (ear), blepharophyma (eyelid). Predominantly affects men.
- Ocular — blepharitis, conjunctivitis, recurrent chalazia, dry eye, marginal keratitis.
- Other phenotypes (granulomatous, neuro-inflammatory, lupus miliaris disseminatus faciei) recognised by some classifications.
Clinical features and triggers
- Onset 30-60 years; female preponderance (except phymatous).
- Triggers: hot drinks, alcohol, spicy food, sun exposure, extremes of temperature, stress, topical irritants, vasoactive drugs.
- Demodex folliculorum density is increased and contributes to inflammation; rationale for topical ivermectin.
- Pearly papules of granulomatous rosacea may mimic BCC clinically.
Differentials important in skin-oncology
- Basal cell carcinoma of the nasal tip — pearly nodule, telangiectasia, ulceration; high index of suspicion within rhinophyma background — dermoscopy and biopsy any persistent papule.
- Cutaneous sarcoidosis — granulomatous papules; consider in resistant disease.
- Lupus erythematosus (malar rash) — photodistribution; lacks pustules; ANA positive.
- Polymorphous light eruption.
- Cutaneous T-cell lymphoma (folliculotropic MF) — facial / scalp; rosaceiform variant rare but described.
- Acne vulgaris — comedones (absent in rosacea); broader age range.
- Perioral dermatitis — sparing of vermilion; less central face.
Management
- Lifestyle: trigger avoidance, daily sun protection (SPF 30+), gentle skincare.
- Topical first-line:
- Metronidazole 0.75% gel/cream BD.
- Azelaic acid 15-20% BD.
- Ivermectin 1% cream OD.
- Brimonidine 0.33% / oxymetazoline 1% for transient erythema control.
- Oral:
- Low-dose doxycycline 40 mg modified release OD (sub-antimicrobial dose) for papulopustular.
- Lymecycline / standard doxycycline 100 mg OD for 6-12 weeks for moderate-severe.
- Phymatous: oral isotretinoin (low-dose), surgical decortication, CO2 laser, dermabrasion.
- Telangiectasia: pulsed dye laser, intense pulsed light.
- Ocular: lid hygiene, ocular lubricants, topical ciclosporin / azithromycin; ophthalmology referral.
Practical points
- Always examine the nasal tip carefully in rhinophyma — BCC may hide within phymatous tissue; dermoscopy / biopsy any persistent papule.
- Sun protection is a critical adjunct because UV both exacerbates rosacea and promotes nasal-tip skin cancer.
- Refer to ophthalmology if any ocular symptoms — untreated ocular rosacea can cause corneal scarring.
- Phymatous decortication: combination of cold-steel debulking and CO2 / Er:YAG laser planing has best aesthetic outcome.
References
- Tan J et al. Updating the diagnosis, classification and assessment of rosacea: recommendations from the global ROSacea COnsensus (ROSCO) panel. Br J Dermatol. 2017;176:431-438.
- NICE CKS. Rosacea. London: NICE; accessed 18 May 2026.
- van Zuuren EJ et al. Interventions for rosacea. Cochrane Database Syst Rev. 2019;3:CD003262.
- Layton AM et al. British Association of Dermatologists guidelines for the management of rosacea. Br J Dermatol. 2024 (in press).
Spot a correction?
If any clinical statement, citation or link on this page needs updating, please email admin@skinoncology.net with the page name, the proposed correction and the supporting source.

