Eritrasma
Published on September 18, 2026
Risk Factors
Obesity, diabetes mellitus, immunosuppression, excessive sweating (hyperhidrosis), tropical/humid climates, advanced age, poor hygiene
Etiology
Corynebacterium minutissimum, a gram-positive rod that colonizes the superficial stratum corneum
Presentation
Asymptomatic or mildly pruritic, well-demarcated reddish-brown to tan patches in skin folds (groin, axillae, inframammary, interdigital web spaces of feet)
Classic Exam
Flat, well-demarcated, reddish-brown macules/patches with fine, wrinkled ("cigarette-paper") scale in intertriginous zones; no raised, active border
Diagnostics
Coral-red fluorescence under Wood's lamp (due to coproporphyrin III produced by the organism)
Management
Localized: topical erythromycin 2% or topical clindamycin 1%. Extensive: oral erythromycin 250 mg QID for 14 days
Keywords
"coral-red fluorescence," "Wood's lamp," "intertriginous," "reddish-brown patch," "fine scale," "Corynebacterium," "diabetic patient with groin rash"
01Pathophysiology
Erythrasma is a superficial bacterial infection of the skin caused by Corynebacterium minutissimum, a gram-positive, catalase-positive, non-spore-forming bacillus that is part of the normal cutaneous flora. The organism proliferates within the uppermost layers of the stratum corneum without invading deeper tissue. This is why erythrasma is a surface-level process with no systemic signs such as fever, lymphadenopathy, or leukocytosis.
The bacterium thrives in warm, moist environments. This explains why the infection localizes to intertriginous areas (groin, axillae, interdigital web spaces, inframammary folds), where skin-on-skin contact traps moisture and heat. Conditions that increase skin surface moisture or compromise local host defenses, particularly diabetes mellitus and obesity, predispose to overgrowth. Diabetic patients have altered skin pH, increased glucose in sweat, and impaired immune surveillance, all of which create an ideal environment for C. minutissimum.
A critical concept for exam purposes is the organism's production of coproporphyrin III, a porphyrin pigment. This pigment is the direct reason for the hallmark coral-red fluorescence under Wood's lamp examination. The connection between pathophysiology and the diagnostic finding is direct: the bacterium's metabolic byproduct is the diagnostic marker.
Because the infection is confined to the dead keratin layer, the inflammatory response is minimal. This explains the lack of vesicles, pustules, or a raised active border, which is a key clinical differentiator from dermatophyte infections (tinea).
02Classification and Clinical Manifestation
Erythrasma does not have a formal staging system, but it is clinically classified by its location and extent.
Intertriginous (classic)
Location
Groin, axillae, inframammary folds
Clinical Features
Well-demarcated, reddish-brown patches with fine wrinkling scale; usually bilateral
Notes
Most common form; often confused with tinea cruris
Interdigital
Location
Toe web spaces (especially 4th-5th)
Clinical Features
Maceration, scaling, and fissuring between toes
Notes
Often coexists with dermatophyte infection; commonly overlooked
Generalized/Discoid
Location
Trunk, proximal extremities
Clinical Features
Widespread, scaly, hyperpigmented patches beyond skin folds
Notes
Rare; seen in immunocompromised or diabetic patients; mimics tinea corporis or pityriasis versicolor
Type | Location | Clinical Features | Notes |
|---|---|---|---|
Intertriginous (classic) | Groin, axillae, inframammary folds | Well-demarcated, reddish-brown patches with fine wrinkling scale; usually bilateral | Most common form; often confused with tinea cruris |
Interdigital | Toe web spaces (especially 4th-5th) | Maceration, scaling, and fissuring between toes | Often coexists with dermatophyte infection; commonly overlooked |
Generalized/Discoid | Trunk, proximal extremities | Widespread, scaly, hyperpigmented patches beyond skin folds | Rare; seen in immunocompromised or diabetic patients; mimics tinea corporis or pityriasis versicolor |
Clinical Pearl: The intertriginous form is the most commonly tested. Vignettes typically describe a diabetic or obese patient with a chronic, mildly itchy, brownish patch in the groin that "hasn't responded to antifungals." That last detail is the strongest clinical clue.
03Diagnostic Workup
Wood's lamp examination
Role
Best initial test and most commonly tested diagnostic step
Expected Finding
Coral-red fluorescence of affected skin
KOH preparation
Role
Adjunct to rule out dermatophyte co-infection
Expected Finding
Negative for hyphae and spores (rules out tinea)
Gram stain of skin scraping
Role
Confirmatory if needed
Expected Finding
Gram-positive rods and filaments in the stratum corneum
Culture on tissue culture media
Role
Gold standard (rarely needed clinically)
Expected Finding
Growth of C. minutissimum (slow-growing, requires enriched media, up to 2 weeks)
Skin biopsy
Role
Rarely indicated
Expected Finding
Gram-positive rods in the superficial stratum corneum; minimal inflammation
Test | Role | Expected Finding |
|---|---|---|
Wood's lamp examination | Best initial test and most commonly tested diagnostic step | Coral-red fluorescence of affected skin |
KOH preparation | Adjunct to rule out dermatophyte co-infection | Negative for hyphae and spores (rules out tinea) |
Gram stain of skin scraping | Confirmatory if needed | Gram-positive rods and filaments in the stratum corneum |
Culture on tissue culture media | Gold standard (rarely needed clinically) | Growth of C. minutissimum (slow-growing, requires enriched media, up to 2 weeks) |
Skin biopsy | Rarely indicated | Gram-positive rods in the superficial stratum corneum; minimal inflammation |
Wood's Lamp Examination is the cornerstone of diagnosis and the answer the exam is almost always looking for. The lamp emits ultraviolet light at approximately 365 nm, causing the coproporphyrin III produced by C. minutissimum to emit a characteristic coral-red (pinkish-red) fluorescence. This test is rapid, non-invasive, and highly characteristic.
One important caveat: the fluorescence can be washed away if the patient recently bathed or applied topical agents to the area. If the vignette mentions a patient who cleaned the area before the visit, this can produce a false-negative Wood's lamp result. This is a testable detail.
KOH preparation is not the diagnostic test for erythrasma, but it plays an important role in the workup. Because the clinical appearance overlaps heavily with tinea cruris and tinea pedis, a negative KOH in the presence of coral-red fluorescence strongly confirms erythrasma and rules out dermatophyte infection. Think of KOH as the test that eliminates the main differential.
Culture of C. minutissimum is technically the most accurate test, but it is slow, expensive, and almost never required in practice. For exam purposes, the answer to "What test confirms the diagnosis?" is Wood's lamp, not culture, because the coral-red fluorescence pattern is considered pathognomonic in clinical context.
04Management and Treatment
Localized disease (first-line)
Treatment
Topical erythromycin 2%
Dose and Duration
Apply twice daily for 14 days
Localized disease (alternative)
Treatment
Topical clindamycin 1%
Dose and Duration
Apply twice daily for 14 days
Localized disease (alternative)
Treatment
Topical miconazole 2% or Whitfield's ointment
Dose and Duration
Apply twice daily for 14 days (mild antibacterial and antifungal properties)
Extensive or recurrent disease
Treatment
Oral erythromycin
Dose and Duration
250 mg four times daily for 14 days
Extensive (alternative)
Treatment
Oral clarithromycin
Dose and Duration
Single dose of 1 g (shown effective in studies)
Recurrence prevention
Treatment
Benzoyl peroxide wash or antibacterial soap
Dose and Duration
Ongoing use in affected areas
Clinical Scenario | Treatment | Dose and Duration |
|---|---|---|
Localized disease (first-line) | Topical erythromycin 2% | Apply twice daily for 14 days |
Localized disease (alternative) | Topical clindamycin 1% | Apply twice daily for 14 days |
Localized disease (alternative) | Topical miconazole 2% or Whitfield's ointment | Apply twice daily for 14 days (mild antibacterial and antifungal properties) |
Extensive or recurrent disease | Oral erythromycin | 250 mg four times daily for 14 days |
Extensive (alternative) | Oral clarithromycin | Single dose of 1 g (shown effective in studies) |
Recurrence prevention | Benzoyl peroxide wash or antibacterial soap | Ongoing use in affected areas |
For localized erythrasma, topical therapy is sufficient and is the first-line approach. Erythromycin 2% cream or solution applied twice daily for 14 days is the standard treatment. Topical clindamycin 1% is equally effective and is a reasonable alternative. The choice between these two is not typically tested; what matters is knowing that localized disease is treated topically with a macrolide or lincosamide.
For extensive, recurrent, or refractory disease, oral erythromycin 250 mg four times daily for 14 days is the treatment of choice. An increasingly cited alternative is a single 1 g dose of oral clarithromycin, which has shown high cure rates and excellent compliance. On exams, if the vignette describes widespread disease or failure of topical therapy, the answer shifts to systemic macrolide therapy.
Adjunctive measures are important for preventing recurrence. The organism thrives in moist environments, so patients should be counseled on keeping intertriginous areas dry, using absorbent powders, wearing loose-fitting clothing, and managing underlying conditions such as diabetes and obesity. Benzoyl peroxide wash or antiseptic cleansers can reduce bacterial load and lower recurrence rates.
Contraindications and Considerations: Macrolides (erythromycin, clarithromycin) carry a risk of QT prolongation and should be used with caution in patients on other QT-prolonging medications. Clarithromycin is contraindicated in pregnancy. If these agents cannot be used, topical therapy with clindamycin or fusidic acid is a safe alternative.
The "Next Best Step" logic for a typical vignette: patient with a chronic reddish-brown groin rash that failed topical antifungals, Wood's lamp shows coral-red fluorescence. The next best step is topical erythromycin 2% (if localized) or oral erythromycin (if widespread).
05Differential Diagnosis and Distractors
Tinea cruris
Why It Is Similar
Also presents as a pruritic, scaly, erythematous groin rash in obese/diabetic patients
Key Discriminator
Tinea has an active, raised, advancing border with central clearing; KOH shows hyphae; Wood's lamp is negative (most dermatophytes do not fluoresce; exception: Microsporum species, which cause scalp tinea, not groin)
Inverse psoriasis
Why It Is Similar
Pink-red, well-demarcated plaques in skin folds (groin, axillae)
Key Discriminator
Inverse psoriasis plaques are brighter red, thicker, and more sharply demarcated with a glazed, shiny surface; no fluorescence under Wood's lamp; often history of psoriasis elsewhere (scalp, elbows, nails)
Seborrheic dermatitis
Why It Is Similar
Can present in intertriginous areas with erythema and scaling
Key Discriminator
Seborrheic dermatitis favors sebaceous gland-rich areas (scalp, nasolabial folds, eyebrows) and has greasy, yellowish scale; Wood's lamp negative
Pityriasis versicolor (tinea versicolor)
Why It Is Similar
Hyperpigmented or hypopigmented scaly patches, also caused by a commensal organism
Key Discriminator
Distribution is on trunk and proximal extremities (not intertriginous); caused by Malassezia; KOH shows "spaghetti and meatballs" pattern; Wood's lamp may show yellow-green fluorescence (not coral-red)
Contact dermatitis (irritant or allergic)
Why It Is Similar
Erythema and scaling in groin/axillae
Key Discriminator
Typically more vesicular, weeping, or eczematous; associated with exposure to irritant/allergen (new detergent, deodorant); no fluorescence
Candidal intertrigo
Why It Is Similar
Red, macerated plaques in skin folds, especially in diabetic patients
Key Discriminator
Candida produces satellite papules and pustules beyond the main plaque margin; KOH shows pseudohyphae and budding yeast; no coral-red fluorescence
Differential | Why It Is Similar | Key Discriminator |
|---|---|---|
Tinea cruris | Also presents as a pruritic, scaly, erythematous groin rash in obese/diabetic patients | Tinea has an active, raised, advancing border with central clearing; KOH shows hyphae; Wood's lamp is negative (most dermatophytes do not fluoresce; exception: Microsporum species, which cause scalp tinea, not groin) |
Inverse psoriasis | Pink-red, well-demarcated plaques in skin folds (groin, axillae) | Inverse psoriasis plaques are brighter red, thicker, and more sharply demarcated with a glazed, shiny surface; no fluorescence under Wood's lamp; often history of psoriasis elsewhere (scalp, elbows, nails) |
Seborrheic dermatitis | Can present in intertriginous areas with erythema and scaling | Seborrheic dermatitis favors sebaceous gland-rich areas (scalp, nasolabial folds, eyebrows) and has greasy, yellowish scale; Wood's lamp negative |
Pityriasis versicolor (tinea versicolor) | Hyperpigmented or hypopigmented scaly patches, also caused by a commensal organism | Distribution is on trunk and proximal extremities (not intertriginous); caused by Malassezia; KOH shows "spaghetti and meatballs" pattern; Wood's lamp may show yellow-green fluorescence (not coral-red) |
Contact dermatitis (irritant or allergic) | Erythema and scaling in groin/axillae | Typically more vesicular, weeping, or eczematous; associated with exposure to irritant/allergen (new detergent, deodorant); no fluorescence |
Candidal intertrigo | Red, macerated plaques in skin folds, especially in diabetic patients | Candida produces satellite papules and pustules beyond the main plaque margin; KOH shows pseudohyphae and budding yeast; no coral-red fluorescence |
06Traps and High-Yield Pearls
The single most common way students miss erythrasma is by defaulting to a fungal diagnosis when they see a reddish-brown, scaly, intertriginous rash. The groin location, the scaling, and the association with diabetes all scream "tinea cruris," and many students pick an antifungal without considering a bacterial etiology. The exam exploits this tendency by including a detail that should redirect your thinking: either a negative KOH prep, a history of failed antifungal therapy, or an outright mention of Wood's lamp with coral-red fluorescence.
Another common trap involves confusing fluorescence colors. Students must commit to memory: coral-red = erythrasma (C. minutissimum), yellow-green = tinea versicolor (Malassezia), and bright green = Pseudomonas. The fluorescence color is the discriminator, and substituting one for another will cost you the question.
A subtler trap is the interdigital form. When a vignette describes scaling and maceration of the toe web spaces, students jump to tinea pedis. The clue is again a negative KOH or a mention of fluorescence. Recognize that erythrasma and dermatophyte infections can coexist in the same web space, so a positive KOH does not automatically rule out concurrent erythrasma.
Finally, remember that the core competency being tested here is pattern recognition of a benign, superficial bacterial skin infection that mimics a fungal process. The exam wants to confirm that you can use Wood's lamp findings and KOH results together to distinguish bacterial from fungal etiologies in intertriginous dermatoses and choose the correct antimicrobial class (antibacterial, not antifungal) for treatment.