What Is Rosacea?
Rosacea is a chronic inflammatory facial disease that predominantly affects fair-skinned adults, with peak incidence between 30-50 years. It is characterized by persistent centrofacial erythema, telangiectasias (dilated vessels), papules, pustules, and episodes of flushing (transient redness).
The disease affects roughly 5-10% of the adult population and is more prevalent in people of Northern European descent. Although it can superficially resemble acne, rosacea has distinct pathophysiology, triggers, and treatment. Unlike acne, it does not present with comedones.
Rosacea is underdiagnosed and frequently underestimated. The psychosocial impact is significant: patients report embarrassment, social anxiety, and reduced self-esteem. Facial burning and stinging can be as disabling as the visible appearance of lesions.
Neurovascular Dysfunction
Hypersensitivity of facial vessels to thermal, emotional, and dietary stimuli causes flushing and persistent erythema.
Dysregulated Innate Immunity
Excess cathelicidin (LL37) and TLR-2 receptor activation generate chronic inflammation in facial skin.
Ocular Involvement
Ocular rosacea affects up to 50% of patients — blepharitis, dry eye, conjunctivitis. May precede cutaneous manifestations.
Pathophysiology
Rosacea results from an interaction among neurovascular dysfunction, dysregulation of innate immunity, and cutaneous barrier alteration. A central finding is the excess of cathelicidin LL-37, an antimicrobial peptide that, at high concentrations, becomes proinflammatory and angiogenic.
The kallikrein 5 (KLK5) enzyme cleaves cathelicidin into proinflammatory fragments. Patients with rosacea show significantly elevated KLK5 and LL-37 in facial skin. TLR-2 receptor activation (by microorganisms or thermal stress) amplifies KLK5 and cathelicidin production, perpetuating the inflammatory cycle.
Demodex folliculorum — a commensal mite of the facial follicles — is present at 5-10 times greater density in rosacea skin. Its proliferation activates TLR-2, contributing to inflammation. Treatment with topical ivermectin (antiparasitic) is highly effective, validating this mechanism. Neurovascular dysfunction involves hyperexcitable TRPV1 channels, which respond exaggeratedly to heat, capsaicin, and alcohol.

Symptoms
Rosacea is currently classified by phenotypes (individual manifestations) rather than fixed subtypes, recognizing that features overlap. Persistent centrofacial erythema and flushing are the most common and defining findings.
Phenotypes of Rosacea
- 01
Persistent centrofacial erythema
Fixed redness across the central face (nose, cheeks, chin, forehead). The main diagnostic criterion of rosacea.
- 02
Flushing (transient redness)
Episodes of intense, transient redness triggered by heat, sun, spicy foods, alcohol, stress, or exercise. May last minutes to hours.
- 03
Papules and pustules
Inflammatory lesions without comedones (the key difference from acne). Centrofacial distribution. May be mistaken for adult-onset acne.
- 04
Telangiectasias
Dilated vessels visible at the skin surface, especially on the alae of the nose and cheeks. Result from chronic angiogenesis.
- 05
Facial burning and stinging
Burning, stinging, and skin sensitivity. Often the most bothersome symptom. Worsens with topical products and sun exposure.
- 06
Phymatous changes (rhinophyma)
Thickened, irregular nasal skin from sebaceous gland hyperplasia and fibrosis. Predominates in men. The most advanced form.
Diagnosis
Diagnosis is clinical, based on the phenotypes present. The main diagnostic criterion is fixed centrofacial erythema that worsens with known triggers. Phymatous changes are also diagnostic on their own.
Dermoscopy can help identify Demodex and differentiate rosacea from other conditions. Biopsy is rarely needed but may be useful to rule out cutaneous lupus and contact dermatitis. Ophthalmologic examination is recommended to screen for ocular rosacea.
DIFFERENTIAL DIAGNOSIS
| CONDITION | DIFFERENCES FROM ROSACEA |
|---|---|
| Acne vulgaris | Comedones present, no flushing, earlier onset |
| Cutaneous lupus | "Butterfly wing" erythema, spares the nasolabial fold, ANA positive |
| Seborrheic dermatitis | Oily scales, affects nasolabial folds and eyebrows |
| Perioral dermatitis | Papules around the mouth, spares the lip border |
| Photodermatosis | Clear relationship with sun exposure, affects exposed areas |
Differential Diagnosis
Rosacea affects the central face and can be mistaken for several other conditions. Fixed erythema, flushing, and absence of comedones are the most important distinguishing features.
DIAGNÓSTICO DIFERENCIAL
Differential Diagnosis
Acne
Read more →- Comedones
- Adolescents
- No background erythema
Systemic Lupus Erythematosus
- Butterfly rash
- Photosensitive
- ANA positive
Testes Diagnósticos
- ANA
- Anti-DNA
Seborrheic Dermatitis
- Greasy scale
- Nostrils and nasolabial fold
Carcinoid
- Episodic flushing + diarrhea
- Elevated serotonin
- Paroxysmal flushing = investigate carcinoid
Testes Diagnósticos
- Urinary 5-HIAA
- Chromogranin A
Polycythemia Vera
- Facial erythema + aquagenic pruritus
- Elevated hematocrit
Testes Diagnósticos
- CBC
- JAK2
Lupus Erythematosus vs. Rosacea: Differences That Matter
The malar rash of systemic lupus erythematosus (SLE) is photosensitive, spares the nasolabial fold, and is often associated with other systemic disease criteria — arthralgia, serositis, cytopenias, proteinuria, and antinuclear antibodies (ANA positive in more than 95% of cases). Clinical overlap with rosacea can be misleading, especially in early stages.
Features that raise suspicion of SLE include marked photosensitivity, joint involvement, disproportionate fatigue, blood-count abnormalities, proteinuria, or positive ANA on screening. ANA is the screening test and, if positive, should be complemented with specific antibodies (anti-double-stranded DNA, anti-Sm). The acupuncture physician systematically investigates these signs to avoid delaying an SLE diagnosis.
Carcinoid and Paroxysmal Flushing: A Red Flag
Carcinoid tumor — a neuroendocrine neoplasm usually of the gastrointestinal tract — produces serotonin and other vasoactive amines that cause episodic facial flushing, diarrhea, and bronchospasm (carcinoid syndrome). Carcinoid flushing is typically dry (without sweating), lasts minutes to hours, may appear reddish or cyanotic, and often has specific triggers (alcohol, cheeses, exercise).
Urinary 5-HIAA (a serotonin metabolite) has 70-80% sensitivity for functioning carcinoid tumors. Serum chromogranin A is a more sensitive marker. Differential diagnosis with rosacea is mandatory in any patient with episodic flushing — especially when accompanied by gastrointestinal symptoms.
Ocular Rosacea: The Frequently Overlooked Subtype
Ocular rosacea occurs in 50 to 60% of patients with cutaneous rosacea and often precedes the cutaneous manifestations. It presents as chronic blepharitis, recurrent conjunctivitis, foreign-body sensation, photophobia, and, in severe cases, keratitis with risk of visual compromise. Diagnosis is frequently delayed because the physician does not link the ocular symptoms to rosacea.
Treatment of ocular rosacea includes meticulous lid hygiene (warm compresses, cleansing with neutral shampoo), ocular lubrication, oral doxycycline and, in severe cases, ophthalmologist follow-up. Every patient with rosacea should be asked about ocular symptoms, and any associated ocular complaint should prompt ophthalmologic evaluation.
Treatment
Treatment of rosacea is directed at the phenotypes present. Identification and avoidance of triggers is fundamental. Topical and/or oral treatment is chosen according to predominant phenotypes: erythema/flushing, papules/pustules, telangiectasias, or phymatous changes.
General Care and Triggers
ContinuousStrict photoprotection (SPF 30+, physical sunscreen). Avoid individual triggers: heat, sun, alcohol, spicy foods, stress. Mild, fragrance-free dermocosmetics for sensitive skin. Thermal water for relief.
Papules and Pustules
Topical +/- oral treatmentTopical ivermectin 1% (first-line): anti-Demodex and anti-inflammatory. Topical metronidazole 0.75%. Azelaic acid 15%. If moderate/severe: doxycycline 40 mg sustained-release/day (anti-inflammatory sub-antibiotic dose).
Erythema and Flushing
Vasomotor treatmentBrimonidine 0.33% gel (alpha-2 agonist): temporary vasoconstriction, effect in 30 min, lasts 6-8 h. Oxymetazoline 1% cream: alternative. Oral beta-blockers (carvedilol, propranolol) for frequent flushing.
Telangiectasias
ProceduresVascular laser (PDL 595 nm or KTP 532 nm) and intense pulsed light (IPL): definitive treatment for telangiectasias. Multiple sessions required. Topical treatments do not eliminate established vessels.
Acupuncture as Treatment
Acupuncture is studied in rosacea for its effects on vasomotor regulation, inflammatory modulation, and stress control — three pillars of the disease's pathophysiology. Modulation of the autonomic nervous system by acupuncture may influence the exacerbated facial vascular reactivity.
Hypothesized mechanisms include modulation of sympathetic vasomotor tone, effects on vasoactive neuropeptides (substance P, CGRP), and mast-cell activation — hypotheses extrapolated from other vascular and inflammatory conditions, with specific data for rosacea still scarce.
In clinical practice, acupuncture may be a complementary option for patients with rosacea in whom stress is a significant trigger, for frequent flushing, and for facial burning. It does not replace topical ivermectin, photoprotection, or treatment of telangiectasias.
Prognosis
Rosacea is chronic and requires long-term treatment. With trigger avoidance and adequate treatment, most patients achieve satisfactory control. Ivermectin and sub-dose doxycycline control papules and pustules in most cases.
Telangiectasias do not respond to topical treatment and require laser or IPL for removal, with good results. Once established, rhinophyma requires surgical or ablative laser treatment. Untreated ocular rosacea can rarely lead to keratitis and visual compromise.
Myths and Facts
Myth vs. Fact
Rosacea is caused by alcoholism.
Rosacea is not caused by alcohol, although alcohol may be a flushing trigger. It is an inflammatory disease with a genetic and neurovascular basis. The 'alcoholic's nose' stigma is unfair and incorrect.
Myth vs. Fact
Rosacea is the same as adult acne.
Rosacea and acne are distinct diseases with different pathophysiology. Rosacea has no comedones, involves neurovascular dysfunction and Demodex, and requires different treatments. The distinction is essential for correct management.
Myth vs. Fact
Rosacea has no effective treatment.
Rosacea has effective evidence-based treatments. Topical ivermectin, sub-dose doxycycline, vascular laser, and photoprotection offer satisfactory control in most patients.
When to Seek Help
Frequently Asked Questions
Frequently Asked Questions
Rosacea is a chronic disease without a definitive cure, but highly controllable with adequate treatment. With regular topical therapy, strict photoprotection, and trigger avoidance, most patients achieve excellent disease control and minimal recurrences. Once established, telangiectasias and rhinophyma require specific procedures to resolve.
The most common triggers vary between patients but include sun exposure, extreme heat, hot beverages, alcohol (especially red wine), spicy foods, intense exercise, emotional stress, temperature swings, and certain cosmetics. Identifying and recording personal triggers is fundamental for disease control.
For rosacea-prone skin, mineral sunscreens (titanium dioxide, zinc oxide) are generally better tolerated than chemical filters, which can sting and worsen erythema. Use fluid, non-comedogenic textures with SPF 30 to 50 daily. Some formulations with niacinamide or a light tint help even out skin tone.
Yes. Acne and rosacea may coexist in the same patient — a condition called acne rosacea. In this case, comedones (characteristic of acne) appear alongside erythema and telangiectasias (characteristic of rosacea). Treatment must address both conditions simultaneously, taking care to avoid overly irritating products that may worsen the rosacea component.
Specific evidence for rosacea is still limited, with few controlled trials. Preliminary reports suggest acupuncture may reduce the frequency and intensity of flushing in some patients, especially when stress is a relevant trigger. Mechanisms are hypothesized from data on other vasomotor conditions. Acupuncture does not replace established dermatologic treatment (topical ivermectin, doxycycline, photoprotection); the acupuncture physician may consider it adjunctively on a case-by-case basis.
Rhinophyma is fibrous and glandular thickening of the nasal skin in advanced rosacea, predominantly in men. It gives the nose a nodular, irregular appearance. Clinical treatment with isotretinoin may stabilize progression. Established rhinophyma requires surgical or laser procedures (ablative CO2, radiofrequency) for tissue remodeling.
Yes. The estrogen drop at menopause can dysregulate thermoregulation, increase the frequency and intensity of flushing, and worsen rosacea's vascular sensitivity. Menopausal hot flashes and rosacea flushing may overlap, making management more complex. Menopausal hormone therapy may, paradoxically, improve both hot flashes and rosacea in some patients.
Ivermectin 1% cream has antiparasitic action (against Demodex folliculorum, a mite that colonizes facial follicles at higher density in rosacea) and direct anti-inflammatory action. Comparative studies show it is superior to topical metronidazole in reducing papulopustular lesions, with a lower recurrence rate. Applied once a day, at night, and well tolerated.
Yes. Mineral makeup based on titanium dioxide and zinc oxide is well tolerated and can help conceal erythema, improving quality of life. Foundations with a neutral or lightly green tint (color correctors) neutralize redness. Avoid products with alcohol, fragrances, acids, and dense comedogenic bases. Remove makeup gently with mild cleansers, without rubbing.
In rosacea, oral antibiotics (doxycycline 40 mg sustained-release — sub-antimicrobial dose — or doxycycline 100 mg) are used for their anti-inflammatory effect, not antimicrobial. Treatment lasts 8 to 16 weeks to control papulopustular lesions. They should not be used continuously for long periods without medical reassessment. Maintenance with topical therapies (metronidazole, ivermectin, azelaic acid) is preferable.
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