Rosacea Diagnosis
Diagnosis
- There are no specific lab tests to confirm diagnosis; hence, the diagnosis is based on patient's history and clinical characteristics
Classification
Phenotype Classification
- Based on phenotypes which are observable features that result from genetic and/or environmental influences
- Classification based on phenotype as recommended by the Global Rosacea Consensus (ROSCO) provides a necessary means of assessing and managing rosacea which is consistent with each individual patient's presentation
- Presence of ≥1 diagnostic or ≥2 major phenotypes (usually in a centrofacial distribution) are required for the diagnosis of rosacea
Diagnostic Phenotypes
- Persistent centrofacial erythema in a characteristic pattern associated with periodic intensification by potential trigger factors
- Most common sign of rosacea
- Personal history, drug history and complete physical examination will help exclude other diagnoses such as lupus erythematosus, seborrheic eczema or steroid-induced rosacea
- Phymatous changes
- Most common form is rhinophyma
- Include glandular hyperplasia, patulous follicles, skin thickening or fibrosis, and bulbous appearance of nose
Major Phenotypes
- Flushing or transient centrofacial erythema
- Trigger/exacebating factors cause neurovascular stimulation resulting to flushing which occurs within seconds to minutes
- Papules and pustules
- Red, dome-shaped papules with or without accompanying pustules, often occurring in crops and primarily located in the centrofacial area
- Telangiectasia
- Cutaneous blood vessels which are enlarged and visible
- Ocular manifestations
- Interpalpebral conjunctival injection
- Lid margin telangiectasia
- Scleritis and sclerokeratitis
- Spade-shaped infiltrates in cornea
Secondary or Minor Phenotypes
- Burning or stinging sensation of the skin
- Typically occurs on erythematous skin without scales
- Dry appearance of the skin
- Central facial skin resemble dry skin appearing rough and scaly
- Edema
- May occur during or after prolonged erythema or flushing due to capillary extravasation during inflammation and may persist for days
- Ocular manifestations
- Evaporative tear dysfunction
- Irregularity of the lid margin architecture
- "Honey crust" and cylindrical collarette accumulation at the base of lashes
Subtype Classification
- Former standard classification of rosacea grouping the most common presentations into:
- Erythematotelangiectatic rosacea
- Inflammatory papulopustular rosacea
- Phymatous rosacea
- Ocular rosacea
- Does not fully cover patient's clinical presentation confounding the assessment of degree of severity
Variant
Granulomatous
- Noninflammatory
- Hard, brown, yellow or red cutaneous papules or nodules of similar size
- May be severe and eventually lead to scarring
Severity Grading Scale
- No firmly established severity grading scale
- Severity of each feature/phenotype must be rated independently
- Physicians give their assessment based on severity of signs and symptoms; duration and extent of disease at the time of examination may also be considered in the evaluation
- Patient participates in the grading by giving the assessment of his/her condition considering the physical manifestations and its impact on quality of life (psychological, occupational and social effects)
- Scales used to assess the severity of rosacea phenotypes are:
- Flushing: Flushing Assessment Tool (FAST) and Global Flushing Severity Score (GFSS)
- Persistent erythema: Clinician's Erythema Assessment (CEA) and Patient's Self-Assessment (PSA)
- Papules and pustules: Lesion counts and Investigator's Global Assessment (IGA)
- Suggested severity scale for papulopustular lesions and facial erythema with or without symptoms
- Mild: <10 papules/pustules with mild erythema
- Moderate: 10-19 papules/pustules with moderate erythema
- Severe: ≥20 papules/pustules with severe erythema
- Severity scale for ocular manifestations
- Mild: Mild blepharitis with lid margin telangiectasia
- Mild-moderate: Blepharoconjunctivitis
- Moderate-severe: Blepharokeratoconjunctivitis
- Severe: Sclerokeratitis, anterior uveitis