DERMATOLOGY

Red Rashes on Face

Background

  • Prevalence: Red facial rashes are a common presentation in general practice in Australia.
  • Impact: Significantly affects quality of life due to the cosmetic sensitivity of the face.
  • Importance: Accurate diagnosis is essential for appropriate treatment.

Assessment and Diagnosis

  • History and Examination: A thorough history and physical examination are often sufficient to diagnose common facial rashes.
  • Differential Diagnosis: Wide range, categorized by age, morphology, and distribution. Key factors include symptomology, age of onset, rash morphology, and clinical clues.

Common Causes and Clinical Features

  1. Atopic Dermatitis (Eczema)
    • Morphology: Erythema, scale, excoriations, xerosis, lichenification; honey-colored crusts if infected.
    • Distribution: Face, neck, scalp, eyelids (Dennie–Morgan folds), lips (licker’s eczema).
    • Clinical Clues: History of atopy (asthma, allergic rhinitis, eczema), keratosis pilaris on upper arms/thighs, significant itch, predilection for face/neck suggesting aeroallergens.
    • Diagnostic Tests: Clinical diagnosis, bacterial culture if infected, allergen-specific IgE testing, skin biopsy if unclear.
  2. Irritant Contact Dermatitis
    • Morphology: Xerosis, erythema, scale; worse in skin creases.
    • Distribution: Corners of mouth, ala creases; sparing of eyelids, ears, frontal hairline.
    • Clinical Clues: Timeline with new products, over-cleansing, more common in atopic dermatitis patients.
    • Diagnostic Tests: Clinical diagnosis, cessation of irritant products.
  3. Psoriasis
    • Morphology: Well-defined, scaly, salmon-pink plaques.
    • Distribution: Ears, scalp (especially frontal hairline, occipital scalp), extensors, umbilicus, natal cleft.
    • Clinical Clues: Personal or family history of psoriasis, might have seborrhoeic dermatitis.
    • Diagnostic Tests: Clinical diagnosis, skin biopsy if unclear.
  4. Seborrhoeic Dermatitis
    • Morphology: Ill-defined erythema, greasy scale.
    • Distribution: Scalp, forehead, eyebrows, nasolabial folds, conchal bowl, post-auricular.
    • Clinical Clues: History of dandruff, winter flares, relatively asymptomatic.
    • Diagnostic Tests: Clinical diagnosis, skin biopsy if unclear.
  5. Actinic Keratoses
    • Morphology: Ill-defined erythema and scale, hyperkeratotic papules or nodules.
    • Distribution: Photo-exposed sites (nose, cheeks, temples, ear helices); scalp if bald.
    • Clinical Clues: History of chronic sun exposure, asymptomatic.
    • Diagnostic Tests: Skin biopsy, especially for hyperkeratotic or indurated lesions.
  6. Acne
    • Morphology: Polymorphic erythematous papules, pustules, nodules; comedones, postinflammatory pigmentation, scars.
    • Distribution: Face, back, chest.
    • Clinical Clues: Onset around puberty, family history of acne, possible steroid use.
    • Diagnostic Tests: Clinical diagnosis.
  7. Rosacea
    • Morphology: Erythematous papules, pustules; telangiectasia, erythema.
    • Distribution: Dorsum of nose, cheeks, chin, forehead.
    • Clinical Clues: Flushing with heat, alcohol, spicy food; family history of rosacea.
    • Diagnostic Tests: Clinical diagnosis.
  8. Malassezia Folliculitis
    • Morphology: Monomorphic erythematous papules, pustules based around hair follicles.
    • Distribution: Forehead, chin, lateral cheeks, central face spared.
    • Clinical Clues: Oily skin, flares with heat, sweat, occlusion.
    • Diagnostic Tests: Clinical diagnosis, yellow–orange fluorescence on Woods lamp, KOH test of skin scrapings.
  9. Pseudofolliculitis Barbae
    • Morphology: Erythematous papules, sterile pustules around hair follicles.
    • Distribution: Beard area (cheeks, upper lip, chin, neck).
    • Clinical Clues: Hair removal practices, curly hair, common in men of African ancestry.
    • Diagnostic Tests: Clinical diagnosis, bacterial culture, fungal scrapings.
  10. Sunburn
    • Morphology: Erythema, edema, blistering in severe cases; peeling and flaking during resolution.
    • Distribution: Photo-exposed sites (face, trunk, limbs).
    • Clinical Clues: Associated with sun exposure, sharp cut-off from clothing.
    • Diagnostic Tests: Clinical diagnosis.
  11. Periorificial Dermatitis/Steroid-Induced Rosacea
    • Morphology: Numerous papules, pustules; erythematous, oedematous, scaly.
    • Distribution: Around orifices (mouth, nose, eyes), sparing vermillion border.
    • Clinical Clues: Steroid exposure, paradoxical flare with cessation.
    • Diagnostic Tests: Clinical diagnosis.
  12. Tinea Faciei
    • Morphology: Annular eruption, leading edge, central clearing, peripheral scale.
    • Distribution: Face, neck, scalp.
    • Clinical Clues: Paradoxical worsening with steroids, recent barber visit, pets with scaly patches.
    • Diagnostic Tests: Skin scrapings for fungal microscopy and culture, skin biopsy if unclear.
  13. Allergic Contact Dermatitis
    • Morphology: Oedema, erythema, vesicles or bullae.
    • Distribution: Eyelids, lips, neck, other exposed areas.
    • Clinical Clues: Triggered by products/chemicals, itch.
    • Diagnostic Tests: Clinical diagnosis, allergy patch testing, skin biopsy if unclear.
  14. Shingles
    • Morphology: Erythematous papules, macules; vesicles, crusting.
    • Distribution: Dermatomal, unilateral.
    • Clinical Clues: Burning, pain or tingling before rash, systemic symptoms.
    • Diagnostic Tests: VZV swab for PCR.
  15. Cutaneous Lupus
    • Morphology: Smooth, erythematous plaques (acute); scaly hyperpigmented plaques with follicular plugging (discoid).
    • Distribution: Butterfly distribution (cheeks, nose), other photo-exposed areas.
    • Clinical Clues: Systemic lupus symptoms.
    • Diagnostic Tests: Skin biopsy, ANA, ENA, dsDNA, complement, urine microscopy.
  16. Dermatomyositis
    • Morphology: Pink to violaceous erythema of eyelids, scaling on scalp.
    • Distribution: Eyelids, forehead, scalp.
    • Clinical Clues: Muscle weakness, photosensitivity, other signs of dermatomyositis.
    • Diagnostic Tests: Skin biopsy, CK, myositis-specific antibodies, malignancy screening.
  17. Systemic Conditions (e.g., pulmonary hypertension, liver failure, SVC obstruction, carcinoid syndrome)
    • Morphology: Plethora, fixed erythema, edema, flushing.
    • Distribution: Variable, can involve cheeks, forehead, periorbital region, neck.
    • Clinical Clues: Known comorbidities, systemic symptoms (dyspnea, weight loss, jaundice).
    • Diagnostic Tests: ECG, liver function tests, full blood count, renal function test, chest X-ray, echocardiogram, 24-hour urinary 5-HIAA.

Causes of red rashes on the face
DiagnosisMorphologyDistributionClinical cluesDiagnostic tests
Atopic dermatitis (eczema)Erythema, scale, excoriations, xerosisLichenification
Ill-defined plaques
Honey-coloured crusts if secondarily infected
Anywhere on face, neck, scalp

Variants:
– NeckLips (eg licker’s eczema)
– Eyelids (eg Dennie–Morgan folds)
– Might have eczema elsewhere (eg flexures, nipples, palmoplantar [dyshidrotic eczema])
History of atopy (eg asthma, allergic rhinitis, eczema [including in family members])

Keratosis pilaris on upper arms/thighs

Lichenification suggestive of chronicity
Itch can be significant

Predominance of face/neck eczema might suggest aeroallergens (eg dust mites, pollen, grasses, animal dander)
Clinical diagnosis

Bacterial MCS if secondarily infected
Allergen-specific IgE testing for common aeroallergens if indicated

Skin biopsy: histopathology if diagnosis unclear
Irritant contact dermatitisXerosis
Erythema and scale might be present
Worse in skin creases (eg corners of mouth, ala creases)

Sparing of eyelids, ears, frontal hairline or neck if irritant not in contact with those areas
Timeline with use of one or more new products
Over-cleansing of face
Might or might not be itchy
Patients with atopic dermatitis more prone to developing irritant contact dermatitis
Might have single exposure to strong irritant or chronic exposure to weak irritants
Clinical diagnosis

Cessation of new or unnecessary products and gentle skin care (eg bland unscented moisturiser, sunscreen)
PsoriasisWell-defined, scaly, salmon-pink plaques
Scale can be significant especially in scalp
Favours ears and scalp (especially frontal hairline and occipital scalp)
Might have psoriasis elsewhere (eg extensors, umbilicus, natal cleft, palmoplantar)
Mostly asymptomatic but can be itchy
Concurrent seborrhoeic dermatitis (sebopsoriasis)

Personal or family history of psoriasis
Clinical diagnosis

Skin biopsy: histopathology if diagnosis unclear
Seborrhoeic dermatitisIll-defined erythema, greasy scaleFavours seborrhoeic areas: scalp, forehead, eyebrows, nasolabial fold, conchal bowl, post-auricularHistory of dandruff or flaking scalp
Other sites might be involved including chest, axillae
Can be itchy if inflamed, otherwise relatively asymptomatic
Winter flares with improvement in summer
Clinical diagnosis

Skin biopsy: histopathology if diagnosis unclear
Actinic keratosesIll-defined erythema and scale
Might be discrete or confluent to involve large areas
Hyperkeratotic papules or nodules in some areas
Photo-exposed sites (eg nose, cheeks, temples, ear helices); scalp involvement if bald or thin hair
Might have actinic keratoses elsewhere (eg dorsal hands, forearms, lower legs
Sparing of photoprotected sites
Asymptomatic
Gradual onset over time
History of chronic sun exposure/limited photoprotection
No history or other features of primary dermatosis
Skin biopsy: histopathology (particularly for hyperkeratotic, tender or indurated lesions to exclude invasive SCC)
AcnePolymorphic erythematous papules, pustules and nodules
Cysts might be present in severe cases
Closed or open comedones
Post inflammatory pigmentation
Excoriations (if picking)
Acne scars (eg box car, rolling, atrophic, ice pick scars)
Favours face, back and chestFamily history of acne
Papules, pustules and nodules are in different stages of evolution
Teens: onset around puberty
Adults: persistence since teens or onset early 20s. In women, might flare with menses
Might be associated with testosterone or anabolic steroid usage
Clinical diagnosis
RosaceaMonomorphic erythematous papules and pustules (papulopustular subtype)
Absence of comedones (unless there is co-existing acne)
Telangiectasia and erythema (in erythematotelangiectatic subtype)
Favours dorsum of nose, cheeks, chin, foreheadFavours fair-skinned patients
Might be associated with flushing
History of sensitive skin to various products
Flares with sun exposure
Family history of rosacea
Clinical diagnosis
Malassezia folliculitisMonomorphic erythematous papules and pustules based around hair follicles
Absence of comedones
Favours forehead, chin, lateral cheeksCentral face usually spared
Chest and back might be involved
Might have other forms of cutaneous Malassezia spp. overgrowth (eg seborrhoeic dermatitis, pityriasis versicolour)Oily skin
Flares with heat, sweat, occlusion or in hot, humid conditions
Might be itchy
Clinical diagnosis

Yellow–orange fluorescence on Woods lamp

Skin scrapings of a pustule, KOH test (culture not routinely performed because isolation and culture of Malassezia spp. is difficult)
Pseudofolliculitis barbaeErythematous papules and sterile pustules based around hair follicles
Associated ingrown hairs
Postinflammatory pigmentation
‘Beard’ area of the face (ie cheeks, upper lip, chin, neck)Flares with hair removal (eg shaving, waxing, plucking)Favours patients with curly hair
Most common in men with African ancestry
Might be itchy
Clinical diagnosis

Bacterial MCS to exclude bacterial folliculitis
Fungal skin scrapings to exclude tinea barbae
SunburnAcute phase: erythema and oedema; blistering in severe cases
Resolution phase: peeling and flaking of affected skin
Photo-exposed sites (eg face, trunk, limbs)Sharp cut-off and sparing of areas covered by clothing
Associated ephelides or lentigines (if chronic) in sun-exposed sites
Associated with total duration of sun exposure and UV index
Favours patients with lighter skin phototype
Might be more likely to occur if taking photosensitising medications
Clinical diagnosis
Periorificial dermatitis/steroid-induced rosaceaClassically numerous papules and pustules; might be more confluent than rosacea
Absence of comedones
Might be erythematous, oedematous and scaly in some cases
Clustered around orifices (eg skin inferior to nostrils, chin, lateral cheeks/temples around eyelids)Sparing vermillion border of lipMight be associated with steroid exposure (eg topical mid- to high-potency steroids). Other triggers include intranasal/inhaled or oral steroids
Paradoxical flare with cessation of steroid
Associated stinging or burning sensation
Clinical diagnosis
Tinea facieiAnnular eruption with a leading edge, central clearing and peripheral scale
Might become non-scaly/non-specific if treatment modified with topical steroids (tinea incognito)
Anywhere on face, neck, scalpParadoxical worsening with use of topical steroids
Asymmetrical
History of recent visit to barber
Pets with scaly patches of hair loss (eg cats, dogs, guinea pigs)Might have associated onychomycosis
Skin scrapings for fungal microscopy and culture
Skin biopsy (if required): histopathology
Allergic contact dermatitisAcute phase: oedema, erythema, vesicles or bullae
Chronic phase: mimics atopic dermatitis (erythema, scale, excoriations, lichenification)
Common sites: eyelids, lips/perioral skin, neck
Other sites also exposed to allergen might be affected
Can occur to products/chemicals that have previously been tolerated for many months or years, not just newly introduced products
Associated itch
In acute phase might be triggered 24–48 h following exposure to allergen
Ongoing exposure can lead to chronic phase
Clinical diagnosis
Referral for allergy skin patch testing
Skin biopsy: histopathology if diagnosis unclear
ShinglesPrevesicular phase: crops of erythematous papules and macules
Vesicular phase: pustules, vesicles followed by crusting
Favours dermatomal distribution or is unilateral
Might be multidermatomal or disseminated, especially in immunosuppressed patients
Associated burning, pain or tingling sensation precedes skin manifestations
Might be associated with systemic symptoms (eg malaise)Red flags: ocular involvement, facial weakness, ear canal involvement
VZV swab for PCR
Cutaneous lupusACLE: smooth, erythematous, oedematous plaques

DLE: coin-shaped, scaly hyperpigmented plaques, follicular plugging. Might have scarring
Note: subacute cutaneous lupus erythematosus might less commonly present on the face as annular scaly plaques
ACLE: ‘Butterfly’ distribution, namely bilateral cheeks and across the dorsum of the nose, sparing nasolabial folds. Can affect other photo-exposed sites

DLE: face, scalp, conchal bowl and ears. In diffuse form, might occur on trunk
Might have associated systemic symptoms of lupus (eg synovitis, chest pain, shortness of breath)Skin biopsy: histopathology, direct immunofluorescence
Blood tests: ANA, ENA, dsDNA, complement
Urine microscopy: proteinuria, dysmorphic red blood cells, red cell casts
DermatomyositisPink to violaceous erythema of eyelids; might have associated oedema (heliotrope rash)

Erythema, scale and diffuse alopecia affecting the scalp
Eyelids, forehead, scalp
Might have other clinical signs of dermatomyositis (eg shawl sign, V-neck sign, Holster sign, Gottron’s papules, Gottron’s sign, nail fold changes)
Might have associated muscle weakness (except in amyopathic forms)Associated photosensitivitySkin biopsy: histopathology
Special blood tests: CK, myositis-specific antibodies
Consider malignancy screen
Facial erythema secondary to a non-dermatological systemic process (eg pulmonary hypertension, liver failure, SVC obstruction, carcinoid syndrome)Plethora, fixed erythema, oedema, facial flushing
Absence of more specific skin changes such as pustules, papules, scale, vesicles or erosions
Variable distribution

Might present as facial flushing, fixed erythema and telangiectasia involving the cheeks, forehead, periorbital region and/or neck

Might also involve other body sites (eg palmar erythema, spider naevi on chest)
Known respiratory, gastrointestinal or cardiovascular comorbidities
Systemic symptoms such as dyspnoea, hoarse voice, chest pain, weight loss, fatigue, peripheral oedema, diarrhoea and/or jaundice
Abnormal cardiorespiratory
and/or gastrointestinal examination
Depending on suspected cause:

Electrocardiogram
Bloods: liver function test, full blood count, renal function test
Chest X-rayEchocardiogram24-h urinary 5-HIAA for suspected carcinoid syndrome
5-HIAA, 5-hydroxyindoleacetic acid; ACLE, acute cutaneous lupus erythematosus; ANA, antinuclear antibodies; CK, creatine kinase; DLE, discoid lupus erythematosus; dsDNA, double-stranded DNA; ENA, extractable nuclear antigen antibodies; IgE, immunoglobulin E; KOH, potassium hydroxide; MCS, microscopy, culture, sensitivity; PCR, polymerase chain reaction; SCC, squamous cell carcinoma; SVC, superior vena cava; UV, ultraviolet; VZV, varicella zoster virus.
Causes of red rashes on the face categorised by typical age of onset
Age 20–40 yearsAge 40–60 yearsAge >60 years
Common:
Acne vulgaris
Atopic dermatitis
Rosacea
Seborrhoeic dermatitis
Periorificial dermatitis/steroid-induced rosacea
Irritant contact dermatitis
Sunburn

Less common:
Psoriasis
Allergic contact dermatitis
Malassezia folliculitis
Pseudofolliculitis barbae
Tinea faciei
Cutaneous lupus erythematosus
Seborrhoeic dermatitis
Rosacea
Irritant contact dermatitis
Allergic contact dermatitis
Actinic keratosis
Shingles
Cutaneous lupus erythematosus
Dermatomyositis
Seborrhoeic dermatitis
Atopic dermatitis
Psoriasis
Actinic keratosis
Shingles
Cutaneous lupus erythematosus
Dermatomyositis

Approach to Diagnosis

  1. History of Presenting Issue:
    • Clarify onset, symptomology, effects on quality of life.
    • Assess age of onset and pattern of involvement.
    • Evaluate distribution for possible causes.
  2. Examination:
    • Characterize distribution and predominant morphology.
    • Classify rashes under scaly, papulopustular, and mixed morphology.

Suggested approach to red rashes on the face.

Figure 1. Suggested approach to red rashes on the face.


Causes of red facial rashes categorised by predominant morphology.

Figure 2. Causes of red facial rashes categorised by predominant morphology.


Clinical Clues:

  • Use targeted questions to narrow differential diagnosis based on history and examination findings.

Investigations:

  • Swabs for bacterial culture.
  • Skin scrapings for fungal microscopy and culture.
  • Swab for VZV PCR.
  • Skin biopsy for unclear diagnoses or non-responsive cases.

Conclusion

  • Accurate diagnosis of red facial rashes can often be achieved through a thorough clinical assessment, supported by appropriate investigations when necessary.

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