Acral Acanthosis Nigricans

Acral Acanthosis Nigricans
Acral Acanthosis Nigricans
Acral Acanthosis Nigricans

Acral Acanthosis Nigricans (AAN) is a rare and typically benign skin condition that presents as hyperpigmented, thickened, velvety patches on the skin — specifically on the acral areas (i.e., the extremities like the hands, feet, fingers, and toes).


Key Features of Acral Acanthosis Nigricans

FeatureDescription
LocationDorsal surfaces of hands, feet, fingers, and toes
AppearanceHyperpigmented (brown to black), thickened, velvety plaques
OnsetUsually gradual and asymptomatic
SymptomsGenerally asymptomatic, may have mild pruritus (itching) in some cases
HistologySimilar to other forms of acanthosis nigricans: papillomatosis, hyperkeratosis, and acanthosis

Causes and Associations

Acral Acanthosis Nigricans is often classified as benign and is not typically associated with internal malignancies, unlike the malignant form of AN.

Common associations include:

  1. Ethnicity:

    • More prevalent in individuals with darker skin tones, particularly of African descent.

  2. Genetic Predisposition:

    • Can be idiopathic or familial.

  3. Endocrine Associations:

    • Less commonly associated with insulin resistance or metabolic syndrome than other AN variants.

  4. Drug-Induced:

    • Rarely, can be associated with medications (e.g., nicotinic acid, insulin, or corticosteroids).


Differential Diagnosis

  • Malignant Acanthosis Nigricans (usually involves mucosa and is more widespread)

  • Confluent and Reticulated Papillomatosis

  • Lichen Planus

  • Tinea nigra

  • Post-inflammatory hyperpigmentation


Management

Since AAN is often benign and cosmetic, treatment is generally not required unless for aesthetic or symptomatic reasons.

Options include:

  • Topical keratolytics (e.g., salicylic acid, urea)

  • Topical retinoids (e.g., tretinoin)

  • Laser therapy (for cosmetic purposes)

  • Treating underlying causes (if identified)


Prognosis

  • Usually benign with a stable or slow progression.

  • Not considered a marker for malignancy or systemic disease in most cases.

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