To minimize the appearance of pigmented lines and wrinkles on the knuckles and elbow creases, the approach depends on the underlying cause, which is often benign but can be associated with systemic conditions such as diabetes, insulin resistance, or autoimmune disease. The pigmentation in skin creases is commonly seen in conditions like acanthosis nigricans, which is most frequently linked to insulin resistance or diabetes, but can also be a feature of other disorders such as autoimmune Addison disease. Key steps to address pigmented creases: Evaluate for underlying systemic disease: Assess for diabetes, insulin resistance, or autoimmune conditions such as Addison disease. If present, management of the underlying condition is the primary treatment. Topical treatments: For benign pigmentation, topical agents such as hydroquinone (Melanex, Lustra), tretinoin (Retin-A), or azelaic acid (Azelex, Finacea) may help lighten hyperpigmented areas. These should be used with caution and under supervision, especially in sensitive areas. Laser and light therapies: Fractional laser or intense pulsed light (IPL) therapy can be considered for persistent pigmentation, but results vary and there is a risk of post-inflammatory hyperpigmentation, especially in darker skin types. Moisturization and sun protection: Regular use of emollients and broad-spectrum sunscreen can help prevent further darkening and protect the skin barrier. Why does it look this way? Pigmented lines and wrinkles in skin creases are often due to increased melanin deposition, which can be a normal variant, especially in darker skin types, or a sign of underlying metabolic or endocrine disease such as diabetes, insulin resistance, or Addison disease. In Addison disease, hyperpigmentation is especially prominent in areas of friction, such as knuckles and elbow creases, due to increased ACTH stimulating melanocytes. In diabetes and insulin resistance, acanthosis nigricans presents as velvety, hyperpigmented plaques in flexural areas. If the pigmentation has been present since childhood and is not associated with systemic symptoms, it is more likely to be a benign variant, but a thorough evaluation is warranted to rule out underlying disease.