What are the distinguishing features between erythrasma and inverse psoriasis (inverse psoriasis)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: May 2, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Differential Diagnosis for Erythrasma and Inverse Psoriasis

When attempting to differentiate between erythrasma and inverse psoriasis, it's crucial to consider various factors, including clinical presentation, patient history, and diagnostic tests. Here's a structured approach to the differential diagnosis:

  • Single Most Likely Diagnosis:
    • Inverse psoriasis: This is often considered due to its common presentation in intertriginous areas (skin folds) with erythematous, smooth, and shiny plaques, which can closely resemble erythrasma. The presence of psoriatic lesions elsewhere on the body and a positive family history can support this diagnosis.
  • Other Likely Diagnoses:
    • Erythrasma: Characterized by well-demarcated, brownish-red, slightly scaling patches in intertriginous areas. It is caused by bacterial infection (Corynebacterium minutissimum) and can be diagnosed with a Wood's lamp, which shows coral-red fluorescence.
    • Intertrigo: A condition involving inflammation of skin folds due to friction, warmth, and moisture, often complicated by fungal or bacterial infections. It presents with erythema, maceration, and sometimes erosions.
    • Seborrheic dermatitis: Although it typically affects the scalp, face, and torso, it can occasionally involve intertriginous areas, presenting with erythematous, oily, scaling lesions.
  • Do Not Miss Diagnoses:
    • Cellulitis: An acute bacterial infection of the skin and subcutaneous tissue, which can present with redness, swelling, warmth, and pain. It requires prompt antibiotic treatment to prevent serious complications.
    • Cutaneous T-cell lymphoma (e.g., mycosis fungoides): Although rare, it can present with patches, plaques, or tumors in the skin, including intertriginous areas, and has a significant impact on prognosis and treatment if missed.
  • Rare Diagnoses:
    • Hailey-Hailey disease (familial benign pemphigus): A rare genetic disorder characterized by blistering lesions in the skin folds due to a defect in the ATP2C1 gene.
    • Darier's disease: A rare genetic disorder that affects the skin and sometimes other areas of the body, presenting with greasy, crusted lesions, particularly in the seborrheic areas and skin folds.

Each diagnosis has distinct features and implications for treatment. Accurate differentiation often requires a combination of clinical evaluation, laboratory tests (including cultures, biopsies, and special stains), and sometimes diagnostic procedures like a Wood's lamp examination.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.