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Acanthosis nigricans

Last updated: April 11, 2024

Summarytoggle arrow icon

Acanthosis nigricans is a dermatological condition of hyperkeratosis characterized by velvety, hyperpigmented plaques that are most frequently located in intertriginous areas such as the axillae or groin. It is often caused by an underlying metabolic or endocrine condition, e.g., diabetes or obesity. Acanthosis nigricans may also be genetic or associated with the use of certain medications (e.g., corticosteroids, oral contraceptives). Benign acanthosis nigricans must be distinguished from malignant acanthosis nigricans, which is the cutaneous manifestation of an underlying malignancy. Acanthosis nigricans is a clinical diagnosis, but testing is indicated to identify the underlying cause. Treatment is focused on the underlying cause and may include cosmetic treatment if requested by the patient.

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Etiologytoggle arrow icon

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Pathophysiologytoggle arrow icon

The stimulation of insulin, IGF, and/or other growth factor (e.g., fibroblast growth factor) receptors leads to epidermal hyperplasia, fibroblast proliferation, and hyperkeratosis. [1][2]

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Clinical featurestoggle arrow icon

  • Appearance [1][2]
  • Location [1][2]

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Managementtoggle arrow icon

Consider underlying malignancy in patients with a severe or atypical presentation (e.g., lesions with rapid onset of lesions, widespread distribution, and/or mucosal surface involvement). [1]

Acanthosis nigricans is a clinical diagnosis. Treatment of the underlying cause can resolve or improve the appearance of the skin lesions. [5][6]

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