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The entities in this chapter can be further classified according to the algorithm in Fig. 89.1 .
Begin to appear during the 4th decade of life and then gradually increase in number.
Macular, papular, or verrucous; colors vary from white to black but most commonly brown.
Typically has a “stuck-on” appearance with a smooth to verrucous surface ( Fig. 89.2 ).
Spares the palms, soles, and mucosal surfaces.
May resemble a melanoma clinically but has no pigment network (by dermoscopy) and has horn pseudocysts.
Sudden appearance of multiple lesions may be associated with internal malignancy ( sign of Leser–Trélat) or erythroderma; the former may also be associated with skin tags, irritated seborrheic keratoses, tripe palms, and acanthosis nigricans.
Histopathology: a spectrum of different architectures, most commonly acanthotic, papillomatous and hyperkeratotic, or irritated ( Fig. 89.3 ).
Variants:
Dermatosis papulosa nigra ( Fig. 89.4 ): common in dark-skinned individuals; 1- to 5-mm hyperpigmented papules on the face
Stucco keratosis ( Fig. 89.5 ): 1- to 4-mm gray-white papules on the lower extremities (especially dorsal feet and ankles) of older adults
Inverted follicular keratosis : endophytic variant of seborrheic keratosis; tan to pink papule, typically on the face of adults
Clinical term for marked hyperkeratosis arising from a papule or nodule ( Fig. 89.6 ).
The base of the lesion most commonly represents an actinic keratosis or wart, but of the entities in this chapter, a seborrheic keratosis is most common; sometimes the base is a squamous cell carcinoma.
Pink to pink-brown papule or plaque ( Fig. 89.7 ); arises in chronically sun-damaged skin, most commonly on the chest, arms, and shins.
Occasionally multiple.
Clinically mimics basal cell carcinoma or Bowen disease.
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