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Acquired melanocytic nevi are common benign skin tumors composed of melanocyte-derived nevus cells.
Acquired melanocytic nevi are more common in whites than Asians and Africans.
Numbers of acquired melanocytic nevi peak in early adolescence, slowly increase in number until age 30 years, and then regress in elderly people.
Genetic factors, as well as environmental influences, such as increased ultraviolet radiation (e.g., natural sunlight and tanning), determine the number of acquired melanocytic nevi.
Other factors, such as skin injury, immunosuppression, hormones, and medications, have been associated with increased numbers of acquired melanocytic nevi.
Skin disorders, such as lichen sclerosis and epidermolysis bullosa, may be associated with acquired melanocytic nevi.
Most acquired melanocytic nevi occur on sun-exposed areas, although Asians and Africans are more likely to develop nevi on acral sites (e.g., palms, soles, and nails) and the conjunctiva.
Most white adults have between 12 and 20 acquired melanocytic nevi.
Acquired melanocytic nevi are asymptomatic, although they may be irritated by clothing or external trauma.
Junctional nevi are brown to tan macules with preserved skin epidermal markings.
Acquired melanocytic nevi on the palms, soles, and genitalia are usually junctional nevi.
Compound nevi are firm brown papules that may have a smooth or papillomatous surface.
Intradermal nevi are skin-colored to tan papules with a smooth surface.
Nevus spilus is a speckled tan to brown patch with sharply demarcated borders, similar to a café-au-lait macule.
There may be brown papules within the nevus spilus.
Blue nevi are solitary blue to black macules and papules, commonly found on the head and neck.
The dark color is attributed to heavily pigmented melanocytes in the deep dermis.
Spitz nevus is a pink to red-brown dome-shaped smooth papule.
Histologically, Spitz nevi may be difficult to differentiate from melanoma.
Spitz nevi are more common in children.
Acquired melanocytic nevi with a rim of depigmentation are called halo nevi .
An immune response to the melanocytes is responsible for the halo.
Vitiligo is associated with halo nevi.
Halo nevi occur primarily during adolescence.
Wood's lamp examination is helpful to evaluate for associated vitiligo.
A recurrent nevus is an irregularly pigmented macule or papule associated with a scar from a previous procedure.
Recurrent melanocytic nevi appear similar to melanoma.
A skin biopsy should be performed on suspicious pigmented lesions.
Acquired melanocytic nevi arise during childhood until about age 30 years and then slowly regress over a number of years.
Atypical (dysplastic) nevus
Melanoma
Hemangioma
Pyogenic granuloma
Juvenile xanthogranuloma
Acquired melanocytic nevi do not require treatment.
Sun precautions (sunscreen and sun-protective clothing) prevent the occurrence of acquired melanocytic nevi.
Pigmented nevi that are irritated may be removed, although irritation does not induce malignant transformation.
Acquired melanocytic nevi on skin areas with limited sun exposure and newly acquired nevi after age 30 years should be regarded as suspicious.
Spitz nevi in adults should be closely evaluated for melanoma because both are similar histologically.
Adults with halo nevi should have a full skin examination to look for an occult melanoma.
A new “junctional melanocytic nevus” in an adult is suspicious for early melanoma.
An atypical melanocytic nevus is a benign melanocytic nevus with abnormal clinical and histologic features.
Approximately 10% of the U.S. population has atypical melanocytic nevi.
Patients with multiple atypical nevi are at increased risk for melanoma, especially if there is a family history of atypical nevi and melanoma (also known as the familial atypical mole and melanoma syndrome).
Atypical melanocytic nevi may arise at any age and continue up until the sixth decade of life.
Atypical melanocytic nevi show asymmetry, border irregularity, color variation, and larger size (between 6 and 15 mm in diameter).
Atypical melanocytic nevi can appear anywhere in the skin but occur most commonly on the trunk and upper extremities.
Patients with familial atypical mole and melanoma syndrome have atypical melanocytic nevi in sun-protected areas, such as the scalp, groin, buttocks, genitalia, breasts (in women), and the palms and soles.
Many atypical melanocytic nevi may indicate an increased risk for ocular melanoma.
Eruptive atypical melanocytic nevi have been described in patients with immunosuppression, chronic myelocytic leukemia, and HIV.
Histologic evaluation of an atypical melanocytic nevus is difficult and should be performed by a dermatopathologist.
Patients with eruptive atypical melanocytic nevi should be evaluated for HIV and leukemia.
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